CSF Leaks and Spontaneous Intracranial Hypotension
F Michaels
Spontaneous Intracranial Hypotension (SIH) is a condition where a patient gets postural headaches due to a leak of the Cerebrospinal Fluid (CSF) in the spinal membrane. (1) What happens is that the leak causes low CSF pressure within the nervous system, and thus causes a constant string of headaches to the patient. The problem with SIH is that it is very hard to diagnose and there is not a great deal of information on why it occurs. In 1995, a study showed that only one in fifty-thousand people in Minnesota had SIH. It also showed that SIH was more common in women than in men, and that the condition usually developed while the patient was between 40 and 60 years old. (5) When first researching this condition, my two main questions were: Why does it develop and can it be cured? In order to answer these questions, one must first examine how CSF runs through the body and the specific symptoms of SIH.Cerebrospinal Fluid is formed in ventricles of the brain. It moves through the ventricles and leaves the brain at the base, underneath the cerebellum.(2) Then, the fluid moves into the spinal cord and the nerves, and finally returns to the brain. Throughout this time, the CSF is moving through a membrane, called the dura that surrounds the brain and spinal cord. The condition of Intracranial Hypotension (IH) develops when a rupture occurs in the membrane. Thus, the CSF leaks out of the dura, causing a dislocation of the brain downward and "pressure on pain-sensitive structures."(5) IH can develop as a result of brain surgery, spinal surgery, or any major trauma to the head. (3) However, as in the case of SIH, the rupture can sometimes occur spontaneously. In other words, there is no known cause for the rip in the dura. Some doctors speculate that the spontaneous tear is due to the initial weakness of the dura, or a traumatic event that went undetected; however there is not a great deal of information on this subject.(5)
The principal symptom of Spontaneous CSF leaks is headaches. The headaches only occur when the patient is upright, and gradually disappear when the patient is lying down. In most cases, the headaches gradually increase from the moment the patient wakes up in the morning. However, in other cases the headaches are quick and severe. The acuteness of the headaches varies in each case, which affects how quickly the condition is diagnosed. Some of the related symptoms of SIH are a loss of hearing, tinnitus, vertigo, stiffness of the neck, nausea, and even vomiting.(5)
Since the primary symptom of SIH is constant and severe headaches, it is often misdiagnosed. Unfortunately, misdiagnosis can increase the painful treatment for other conditions that imitate SIH (such as Chiari malformation) as well as the possibility for early treatment. In a study done by Dr. Wouter I. Schievink between 2001 and 2002, he found that 94% of patients who had SIH were initially misdiagnosed when they visited a doctor about their symptoms.(4) Some of the common treatments due to misdiagnosis included craniotomies (surgical incisions in the skull) and cerebral arteriographies (a procedure that uses an injection of dye and x-ray images to examine arteries in the brain). More than half the number of cases of SIH has been reported in the last decade.(5) Therefore, because SIH is so often misdiagnosed, it is not likely that there has been a drastic increase of the condition, but rather that more cases of it are being correctly diagnosed.
In some cases of SIH, the condition disappears as spontaneously as it appeared. Mild cases can be cured through a general increase in fluids, especially caffeine, and lots of rest. However, more serious cases will require a procedure called the epidural blood patch. This is a procedure where autologous blood is injected into the patient's lumbar spine. The blood travels through the spinal cord, finds the rupture in the dura, and clots the rupture. Success of the epidural blood patch in patients with IH can usually be determined immediately after the procedure. If it is not successful, the procedure can be repeated several times with a larger amount of blood injected (no more than 30 ml) and in many cases can lead to a permanent closing of the torn dura. (5)
However, in more severe cases of Spontaneous Intracranial Hypotension, the epidural blood patches that are injected into the lumbar spine are ineffective. At this point, an effort to locate the exact position of the rupture in the membrane can be made and then another epidural blood patch may be performed at that location.(5) This location-specific procedure is more effective than a regular epidural blood patch, and should cure the condition. However, there are a few cases where even this procedure is not successful. Further procedures to resolve the issue include an injection of fibrin glue into the specific location of the rupture and (in the most persistent cases) even surgery, both of which seem to cure the condition.(5)
In conclusion, Spontaneous Intracranial Hypotension is a very rare type of a Cerebrospinal Fluid leak, but unlike other types, it does not occur due to any specific traumatic event or surgical procedure in the nervous system. Although there is not much information on the possible causes of SIH, it is suspected that an intrinsic weakness of the spinal membrane or an abnormality of the brain structure causes the rare condition. The symptoms of SIH are so small and so common, that it can often be misdiagnosed. Therefore, the condition of SIH, although thought to be very rare, is probably more likely than one might think. So how can someone prevent SIH? Is there anything a person cando to prevent the rupture of the dura? Unfortunately, there is no clear answer because very little information exists as to the primary cause of the tear. All one can really do is avoid brain surgery or any head trauma that could trigger the onset of regular IH. Hopefully, as more observations are gathered about Spontaneous Intracranial Hypotension, the causes of it will be identified and the ways to help prevent it will become more apparent.
References
1)Abstract of two cases by T.A. Rando and R.A. Fishman, general information on SIH2)Discovery Health: CSF leak, general information on Cerebrospinal Fluid leaks
3)University of Maryland Medical Center, general information on Cerebrospinal Fluid leaks
4)Archives of Neurology, Abstract of a study on the Misdiagnosis of SIH
5)Medscape: Spontaneous CSF leaks, A review by Dr. Wouter I. Schievink
08/31/2005, from a Reader on the Web I have had this exact problem. It started in February 2004 and I have had it and the really bad headaches since then. Just recently, my headaches has subsided. A little background: I woke up one day in February 2004 with a excruciating headache. I went to numerous doctors and they all said it was migraine headaches. They gave me many different pain killers and nothing worked. Finally I went to a neurologist. After giving him my simptons, he said "let's check your spinal fluid." He then proceded to put a big needle in my back to check and have my spinal fluid analyzed. He got very little out of my back. He had a lab run some test, but everything came up negative. He gave me some pain killers, that did not work and then that was it. So I went to this other neurologist and he said that he had a patient two months prior that had the same condition and we should try a blood patch. Did that and that did not work, he had me try it again and that did not work. He then suggest that I check into the hospital and run a boat load of tests. He then consulted with another doctor and with all the different tests (MRI, Cat scans, etc) noticed that I had holes in the back of my neck. Both doctors decided that I would stay in the hospital and have my spinal fluid drained every hour and lay flat in the hospital bed to see if the dura would close. After a week and a half in the hospital, they did another test and some of the tear closed but I still had some still torn. (Mind you, I had many tears in the back of my neck and slightly down my spine). I was released from the hospital with the same headaches and continued to live with them until this day, though less severe. When I read your piece on spontaneous leaks, I could not believe that I am not the only one out there that has this problem! THANK YOU!!! I don't know what caused my leakes, I have had no trauma, nothing so I am at a loss. I would love to be able to talk to someone about my case and maybe sent my doctor's and hospital's records to you to put in your database to help other people. Lastly, I just read an short article about the actor George Clooney that had the same thing. I would be great to here more on this subject. I a wait your response. Sandra 11/10/2005, from a Reader on the Web I had a Sponaneous Spinal Fluid Leak in 2003 for which I finally received a blood patch procedure after suffering for 3 weeks through countless tests. I have tinnitus as a result of this condition which began 2 weeks after the initial spinal headache. I was wondering if any one else has this same problem. Its very hard to find information on this since Spontaneous Leaks are so rare (1 in 50,000). I would appreciate learning more about this. 12/30/2005, from a Reader on the Web Comment on the article on CSF leaks and hoping the person who posted a comment will read this one, or perhaps someone at Serendip could forward it to him/her. No, you are not alone with suffering a CSF leak and yes, they can be very hard to find and fix. Here's the link to a discussion community of fellow sufferers and those who suspect they have a leak and don't know. There are a lot of great resources here to help you go back to your Dr's and get more help. Two blood patches is often just the beginning of treatment, not the end, but many neurologists are not up on their reading on this rare problem and don't know what else can be done, or perhaps have never done it themselves and don't want to refer you..... http://brain.hastypastry.net/forums/forumdisplay.php?f=118 Pam Bryan |
Additional comments made prior to 2007
I also have intracranial hypotension from two epidural shots for a lumbar disc problem. The back problem is not so bad anymore but I still suffer from moderate to severe head pressure 24/7. For two years I was bedridden with this terrible ailment, unable to stand along with many of the cranial nerve side effects (double vision, nausea, radicular neuropathy). Three blood patches failed to help....slowly over time I was able to do more. Myelograms and cisternographies have not been able to see my leak, though my spinal pressure was measured twice to be low, as well as my brain mris showing enhancement. Though I am functional again I still have many restrictions including exercise (frustraing as an ex-athlete). I'm also a licensed nutritonist and your paper touches on some interesting points....why doesn't the dura heal? The biggest obstacle with this conditon is the difficulty with diagnosis because most doctors believe the dura must heal in x amount of time and. So to accept that this doesn't occur with everyone is one problem and then why it isn't healing is another. I wonder if certain fundamental factors are missing relating to connective tissue. Not necessarily one of the conventional connective tissue disorders but something missing or interfering with attaining adequate amino acids to fully optimize connective tissue sythesis/regeneration. At any rate, this can be an unbelievably debilitating condition....check out Mass General Hospital's neurology department's...brain forum and look under csf leak diagnosis and you will see it is more common than perhaps once thought. Plus these headaches are so not like migraine, although it is not uncommon for migraines to develop on top of them. These headaches/pressure are all about physics...an intense pulling sensation..like G-forces pulling your head down. I'm praying for more research....maybe better imaging to find smaller leaks. Many thanks for your paper ... Cindy, 4 February 2006
It's wonderful to read the comments from others who have suffered with spinal leaks. I too went misdiagnosed for well over a year. I was told my headaches were caused by stress, menapause or even migranes. It was just one year ago that the pain became unbearable and my doctor now thought it was meningitis. I was put in the hospital and a neurologist found my leak. Although my surgery was to take place in another hospital, it was postponed because I had seizured. I was put into a medically induced coma so I could be stablized. I had never had a seizure in my life and it was believed that it was brought on by the extreme loss of fluid. My leak was at the base of my spine. After an extended hospital stay and complications, I am now happy to say I am cured. I have not had even the slightest headache in one year and hope I never do ... Julie L, 7 April 2006
My husband started w/ severe fatigue approx 4. months ago. The fatigue lessened,but he began having chronic headaches.He has had a headache now for about 3 months. Spinal tap results came back as low pressure and high protein. He seems to think it is a low pressure headache. This is all new to us. We have never heard of such a thing. Apparently there are more of you out there who suffer from this. We would love to hear from anyone experiencing the same thing. He did have a blood patch today. Waiting to see if it helps. Thanks for that great article. Very good and informitive ... Lisa, 15 August 2006
REGARDING SPONTANEOUS INTRACRANIAL HYPOTENSION I am a 36yo female I have had this condition also on july 19 2006 I went to bed with a bad headache and woke up the next morning with sore shoulders and neck when I tried to get up I suffered the most excruciating pain in my neck and head it was so bad I wanted to vomit . When I visited the local hospital the doctor gave me panadol and sent me home without doing any tests. After 3 days of getting worse I went back to my doctor by this time I could barely walk because the pain was so severe the doctor sent me over for a cat scan which they picked up immediatley as some kind of fluid on my brain . After that I was flown by Royal Flying Doctor to Perth . While there I had 2 MRI one on my brain and the other on my spine after the spinal one they picked up that I had a leak in my spine. I just want to tell any one out there who has had or does have this condition that I really feel for you because it's such a traumatic illness and no one has any idea how painful it is also anyone who is suffering pain in the head so bad please demand you have a cat scan ... Deanne, 26 September 2006
I am just three weeks out of having a disctectomy done. The week prior to that I received an epideral to try amd fix the blown disc that I had. Is there anyway to minimize the pan of the headaches? I am being admitted into the hospital again on Monday to now correct the spinal fluid leakage problem. Does anyone have any suggestios concerning this matter or that can supply me with any kind of information? ... Heather, 22 November 2006
I would like to talk to others who are suffering from spinal fluid leaks. Can you help put me in touch? Or, can I talk to you? ... Brad Hennenfent, 22 January 2007
I read the article on Spontaneous Intracranial Hypotension and felt compelled to share my experience with this condition, which is still unresolved but hopefully soon to be treated. I should preface this by saying that I have never had injury or trauma to the head or spine. I developed a headache a little over two weeks ago that was very migraine-like except that none of the pain relievers I tried got rid of it entirely, it originates at the base of the skull and spreads forward, and it's relieved within five minutes of lying down. Also, after five days of the headache, I began to have a feeling of congestion in my ears accompanied by a soft rushing sound, followed by mild hearing loss. The first doctor I saw in Urgent Care gave me some migraine medicine; the second ordered a CT scan; the third ordered a brain MRI and had me see a neurologist; the neurologist saw a report of the MRI that indicated enlarged ventricles, thought I might have hydrocephalus and referred me to a neurosurgeon for another opinion (the neurologist also prescribed Diamox, a diuretic - yikes!); the neurosurgeon looked at my MRI and thought I had a Chiari malformation, but wanted a second opinion so he had me see another neurosurgeon; the second neurosurgeon made the diagnosis of intracranial hypotension and ordered a lumbar MRI to see if they could detect a CSF leak. My dilated ventricles caused a lot of confusion because that's not usually consistent with SIH, but it was eventually concluded that I've probably had hydrocephalus all my life but have never had symptoms, and that the hydrocephalus is not what's causing my current problems. The next step was supposed to be a tracer study to try to identify a leak and its location. Well, my concerned husband got tired of all the shuffling and waiting around among our local doctors, so he took me up to Stanford (about an hour's drive) and checked me in to the ER; as you can imagine, we got much farther much faster by doing that. Stanford neurologists agreed with the diagnosis and have arranged for a blood patch next week -- no messing around with a tracer study. The blood patch will be injected and then my head will be lowered so that the blood coats the entire inside of the dura along the spine, with the assumption that if there's a leak somewhere along there, it will be plugged up. Let's hope it works!!! ... Larisa, 25 March 2007
I AM 45 YEARS OLD AND I TO WIND UP WITH MIGRANES I REMEEMBER JUST THIS MONTH OF THIS YR. MY HEADACHES WERE SO BAD THAT I LAYED IN A DARK COOL ROOM AND JUST SLEPT I WAS FEELING NAUSEATED EVERTIME I HAD TO USE THE RESTROOM THE SMELL OF FOOD EVEN MADE ME SICK. RECENTLY I HAD A MRI AND THE DOCTOR TOLD ME THAT THE FLUIDS IN MY BRAIN WERE LOW. BUT I ALSO WENT THROUGH 3 BLOWS TO THE HEAD FROM MY EX-HUSBAND NOW I HAVE A NEW LIFE A WONDERFULL HUSBAND AND I ALSO TO WENT TO THE COMPUTER TO FIND NUMEROUS ANSWERS BUT NOTHING SEEM COMPLETED I WILL BE SEEING A NEUROLOGIST HERE THIS AUGUST BUT TILL THAN OUR HOUSE IS DARK AND COOL AND TAKE MEDICATION FOR HEADACHES HOW SEVERE CAN THIS BE AND WHAT HAVE THEY FOUND IN TODAY TECHNOLOGY? I HOPE SOMEONE OUT THERE CAN UNDERSTAND WHAT I AM GOING THROUGH AND WHAT RELIEVED DID THEY RECIEVE DURING ALL THIS PLEASE IF ANY ONE KNOWS PLEASE SEND WHAT INFORMATION YOU MAY HAVE CAUSE I WOULD LIKE TO HAVE MY LIFE BACK TO NORMAL ... Susie, 26 June 2007
One morning in Oct. 06 I woke up with severe headaches and after 6 weeks of working up the ladder at my HMO, a neurologist finally diagnosed me with CSF leak (SIH). Not content to being mollified by being put on Prozac, I did some cursory research on the net and found out that others had what I had and found that some had been referred to Dr. Schievink at Cedars Sinai in Los Angeles for treatment. These can include blood patches, glue patches and surgery. His staff is very familiar with the disease and he is "the" expert.
My HMO refused to send me to him (right down the street in my case) the cost you know, until I developed large subdural hematomas. At that point they had no choice but to refer me because it was totally out of their realm to effectively treat the underlying cause, the CSF leak, or the subdurals.
A long story short--after 2 blood patches, 1 glue patch and 2 spinal surgeries(laminectomies)at T9-11 to remove benign Tarlov cysts, to repair 2 leaks, I can now function quite nicely. I have a 20 lb. lifting limit, can't hike up steep hills, and can't push or pull on heavy objects. These modified "val salva" maneuvers, I have learned, will cause undectable (on a CT myleogram) leaks. They come and go because I will still get positional headaches at times. At my last reading my CSF pressure is ZERO.(0) cm.
I'm very fortunate at 60 years old to be retired and thank God every day for the wonderful treatment I have recieved. I think mine was a severe case, I use to do a lot of physical work and ran for 25 yrs and maybe those were contributing factors ... Harvey Geiss, 16 July 2007
I had a spontaneous CSF leak in Nov 2004. After weeks of being told I had migrains, I was sent to a neurologist. He immediatly knew it was a CSF leak and put me on bedrest. After 6 weeks on bed rest, I still had bad headaches everytime I stood up. I then had a test to show where the hole was and they could not find it. I went to a different hospital and asked if we could do the test standing up because that was when I had my pain, and they said their machines can't go up that far. So I asked if they could do it with me on my knees, and they said yes. With in minutes they saw a large tear at C7. After two blood patches my major headaches are gone. From day one, to the last blood patch it was 4 months of bed rest! Yuck! Now I am living my life wondering if this will happen again, and taking Neurontin for these annoying daily headaches. Scary stuff! ... Elizabeth Kilik, 11 October 2007
Reading article and reader comments on intracranial hypotension. I've suffered over past 15 years from initially intracranial hypotension and flipped at some point to intracranial hypertension (or pseudotumor cerebri)! Living in Cleveland, OH diagnosis ranged from CSF leak to Chiari Malformation to POTS to migraine headaches. I ended up at Mayo Clinic where intracranial hypertension was diagnosed JUly 2007. Mayo has some of the leading experts on this area of neurology in the country. Medication was tried for a short while and in August 2007 a VP Shunt was placed to releive the hypertension. Almost 9 weeks after surgery some headache symptoms arise mid-day when I'm upright- started irregularly a few weeks ago now more of a daily occurance, including one episode of nausea and vomiting. I'm following up back at Mayo Clinic in 1 week. Looking for anyone with similar experiences, resolution of symptoms, and return to normal family and work life ... Robert Schneider, 22 October 2007
Comments
acupuncture works
Submitted by Ruth Toops (guest) on Wed, 03/21/2012 - 7:27pm.
Our 13 years old grandson has had a headache since the evening of Jan. 17, 2012. That day he took an inconsequential fall off his bike. He did not hit his head and didn't even mention the fall until several days later when he still had the headache.
We have suspected from the beginning that he had a dura leak; it seemed to match the symptoms, except it did not get better when he was lying down.
The doctors have done MRI, CT scan, EEG, and lumbar puncture, all normal.
On our own (not insurance paid) we went to an acupuncturist who helped him become pain free for several hours. Since then, two treatments a week, average, he is now pain free for 26 hours following each treatment.
The doctors are treating him for migraine, just increasing and increasing the meds which do nothing for him. Children's Hospital, in Los Angeles, basically wrote him off. The neurologist says live with it. He is not able to go to school, be out of bed, or function, except after acupuncture.
That do we do next?
Thank you.
We have suspected from the beginning that he had a dura leak; it seemed to match the symptoms, except it did not get better when he was lying down.
The doctors have done MRI, CT scan, EEG, and lumbar puncture, all normal.
On our own (not insurance paid) we went to an acupuncturist who helped him become pain free for several hours. Since then, two treatments a week, average, he is now pain free for 26 hours following each treatment.
The doctors are treating him for migraine, just increasing and increasing the meds which do nothing for him. Children's Hospital, in Los Angeles, basically wrote him off. The neurologist says live with it. He is not able to go to school, be out of bed, or function, except after acupuncture.
That do we do next?
Thank you.
My dural hole is 3 cm long
Submitted by Serendip Visitor (guest) on Sat, 12/03/2011 - 11:11am.
Possibly acupuncture could work in terms of feeling better, but it certainly will not repair a hole of that size. The osteo defect is even larger. And the herniated brain tissue will not "go back into place."
Acupuncture here costs a lot and without having been able to work now for so many years, I have nothing left. I am eligible for the free food handouts which are comprised of whatever the local grocers are ready to throw out. I have other health issues for which I require medicines not covered by the insurance and cannot afford those. I cannot afford to get my dental work done.
It is all due to the two failed operations which made the defects larger and due to the missing mastoid they pulverized away to get a "good view" and never wasted a moment's thought as to what this woman is going to do afterwards without that part of her skull! At least before the operations and the ear tubes I was able to work! I felt like crap all of the time, but I was still able to function! That has been taken away from me completely.
I am sorry, right before the holiday season, I have nothing, absolutely nothing positive to say about this. There are no alternatives out there accessible to me.
As long as I can stand (which is not very long and not very often) and talk, I need to focus on how to make the voices heard of countless numbers of patients who have been misdiagnosed, not taken seriously and were subject to malpractice.
That is what I need to hear on this forum and anyone out there who has an inkling of where I can direct that energy, please write in.
I no longer believe I will gain access to competent surgeons who can repair that defect.
Acupuncture here costs a lot and without having been able to work now for so many years, I have nothing left. I am eligible for the free food handouts which are comprised of whatever the local grocers are ready to throw out. I have other health issues for which I require medicines not covered by the insurance and cannot afford those. I cannot afford to get my dental work done.
It is all due to the two failed operations which made the defects larger and due to the missing mastoid they pulverized away to get a "good view" and never wasted a moment's thought as to what this woman is going to do afterwards without that part of her skull! At least before the operations and the ear tubes I was able to work! I felt like crap all of the time, but I was still able to function! That has been taken away from me completely.
I am sorry, right before the holiday season, I have nothing, absolutely nothing positive to say about this. There are no alternatives out there accessible to me.
As long as I can stand (which is not very long and not very often) and talk, I need to focus on how to make the voices heard of countless numbers of patients who have been misdiagnosed, not taken seriously and were subject to malpractice.
That is what I need to hear on this forum and anyone out there who has an inkling of where I can direct that energy, please write in.
I no longer believe I will gain access to competent surgeons who can repair that defect.
I found the following link
Submitted by Toni (guest) on Fri, 12/02/2011 - 7:05pm.
I found the following link great! I suggested to my doctor after still not finding my leak creating all of my low pressure headaches to put me on medication that will increase the pressure to balance me out. She let me know that she had discussed my case with a headache specialist and he made the same recommendation. Please check out this link if you are having headaches that go away when you lay down and they happen daily and the pain increases when standing up. I was having sinus pressure and pain, headaches that increased when I was not lying down and no medications over the counter would work. Excedrin extra strength did help take some of the edge off. check it out
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Headaches
Submitted by Serendip Visitor (guest) on Wed, 11/30/2011 - 10:27am.
Most of this summer I have been having really bad headaches. Started with sinus infection that I left untreated for weeks I eventually got medicine and cleared it up. I continued getting headaches daily and then my hearing started to go in my left ear. So I went back to the Dr. They told me that maybe the sinus infection didn't go away so they doubled me up on medications and gave me Prednisone for my ear pain/plugged feeling. While I was on Prednisone I felt amazing. Once I was done with the treatment I started right back up with daily headaches. As soon as I stood up in the morning it would hit me. Sometimes the pain was so severe I was crying on the couch laying down when I should have been getting ready for work. After trying everything I could think of to treat it with no success I finally went to the dr again. The doctor thought that I had sinusitis and ordered a CT scan of my sinuses. When the test came back normal the response was since it was not what was expected she didn't know what to do. I called the Dr. a few days later because they were going to hope I would fall through the cracks. I tried to do my own research and come up with different things that could be wrong. I scheduled an appointment with an allergist, I went to the Chiropractor for an adjustment, and I did research online every night. Going to the Chiropractor was the worst thing I could have done, it brought on the most severe pain I have ever had! I was calling the doctor everyday sometimes in tears. The women at the front would make comments like "your are still in pain". Finally I had to yell at one of the nurses and explained that I am trying to do what the right thing is and threaten to go to the ER daily if they didn't do something and switch doctors. Finally, I was able to see a Dr. that did motor tests and looked in my eyes. When she looked in my eyes she said something was not right. She was able to see where there was pressure or something pressing on the back of my eyes. She got me in for a rush MRI where the outcome was that I have low intracranial pressure. Since I didn't have any injury or trauma they were concerned. It has now been since at least 3 months of daily pain. I still have not received a blood patch and bed rest is killing me.
I guess all I have to say is fight! If you know something is wrong and the doctors just are not helping call them every day and make them do their job!! I finally was able to stop calling daily and for a change they call me. Don't let yourself fall through the cracks.
I guess all I have to say is fight! If you know something is wrong and the doctors just are not helping call them every day and make them do their job!! I finally was able to stop calling daily and for a change they call me. Don't let yourself fall through the cracks.
THANK YOU SO MUCH FOR THAT GET UP AND FIGHT 'EM ATTITUDE!
Submitted by Serendip Visitor (guest) on Thu, 12/01/2011 - 3:25pm.
You have no idea what strength reading these lines has given me!
This is exactly the medicine I need(!): Others who have had to fight, will ADMIT that it IS a battle, that so many doctors are NOT doing their jobs must share to spread hope, and ENERGY TO CONTINUE THE BATTLE.
I honestly do not want to hear about all the "nice" stories which worked out.
I suffer from four serious illnesses: skin cancer, fibromyalgia, spontaneous osteo-dura defect and hernias on both sides.
I write "serious" because they are all potentially life-threatening, including, though indirectly, yes, the fibromyalgia. But I will not go into that here. This forum is for another purpose.
In all four cases I had to search for YEARS to get my diagnoses confirmed. I went running from specialist to specialist, ....oh, you know what, I cannot even bear to repeat it.
What I need to help ME, which is why I am on this forum, also to encourage others who keep hearing it's "all in their head" (yes, it really IS in your head, you have a leak or some other problem!) is to hear from other "fighters" out there who did not give up and got results. I am not talking about healing. I am talking: results! We need to encourage each other not to give up.
To listen to how others are lucky to have such wonderful doctors does not help me one iota here in Munich! I am stuck in this horrible situation and I need to be in contact with and hear stories from people who have gone through the same hell I have.
Thanks so much for lighting the fire within me.....the flame was threatening to go out forever.
Patients are in a weak position. What if patients, except for the emergency and IU cases, simply boycotted doctors and hospital for awhile.
It has gotten to the point where I dread going to see a doctor of any kind. I feel like a mistreated dog, cowering in the corner with its tail between its legs. How could I have let it come to this? Lack of hearing words like yours.
I will keep them in mind when I call again tomorrow.
Sincerely,
Marie
This is exactly the medicine I need(!): Others who have had to fight, will ADMIT that it IS a battle, that so many doctors are NOT doing their jobs must share to spread hope, and ENERGY TO CONTINUE THE BATTLE.
I honestly do not want to hear about all the "nice" stories which worked out.
I suffer from four serious illnesses: skin cancer, fibromyalgia, spontaneous osteo-dura defect and hernias on both sides.
I write "serious" because they are all potentially life-threatening, including, though indirectly, yes, the fibromyalgia. But I will not go into that here. This forum is for another purpose.
In all four cases I had to search for YEARS to get my diagnoses confirmed. I went running from specialist to specialist, ....oh, you know what, I cannot even bear to repeat it.
What I need to help ME, which is why I am on this forum, also to encourage others who keep hearing it's "all in their head" (yes, it really IS in your head, you have a leak or some other problem!) is to hear from other "fighters" out there who did not give up and got results. I am not talking about healing. I am talking: results! We need to encourage each other not to give up.
To listen to how others are lucky to have such wonderful doctors does not help me one iota here in Munich! I am stuck in this horrible situation and I need to be in contact with and hear stories from people who have gone through the same hell I have.
Thanks so much for lighting the fire within me.....the flame was threatening to go out forever.
Patients are in a weak position. What if patients, except for the emergency and IU cases, simply boycotted doctors and hospital for awhile.
It has gotten to the point where I dread going to see a doctor of any kind. I feel like a mistreated dog, cowering in the corner with its tail between its legs. How could I have let it come to this? Lack of hearing words like yours.
I will keep them in mind when I call again tomorrow.
Sincerely,
Marie
Thank you. You have to fight
Submitted by Serendip Visitor (guest) on Fri, 12/02/2011 - 6:52pm.
Thank you. You have to fight for the treatment you deserve now a days and it is mind-blowing how much they get paid for patients having to do all the work. My neurologist says things like "So what do you want to do" my answer always is whatever you recommend I do. ?? Good luck with your fight!
And I thought it was only like that here.....
Submitted by Serendip Visitor (guest) on Fri, 12/02/2011 - 8:33pm.
So this is quite interesting. Patients ALL OVER are getting the same arrogant, inconsiderate treatment.....I honestly thought it was a German thing, or a national insurance problem. (I am writing this fully aware of the fact that NO INSURANCE does not get you anywhere either.....so all those out there against a national insurance plan due to poor treatment they fear they will be subject to, well, even though they have a point there, it does not look like those with the private insurance coverage are getting much better treatment!)
Hey, at least your doctor was nice enough to ASK you what you would like to do as opposed to throwing you out of the office as has happened to me on numerous occasions. Four times I was asked to leave. The other times the doctors simply brushed me off by saying, "you have been dealt a bad hand" and "do not even think for a minute that our insurance system is going to pay for you to go seek the help of some miracle healer in Timbuktu" (this was in response to a question the doctor asked ME. He wanted to know if I had heard of any specialists and I said, yes. When he asked where, I mentioned Dr. Schievink in the U.S. That's when I got the lecture on miracle healers in Timbuktu!
One might say, gee, Marie, maybe it's your attitude....at this point you're d***** right it is! After what I have been through, I have developed a very low opinion of doctors in general and to even hear the word mentioned sets me off. So I had a 9-month time out, WITH therapy to try to make sense of it all. The conclusion is that it makes no sense whatsoever, but to be in a constant state of rage is not helping the situation any. I have an operation of a different nature coming up and in all fairness must say that in this case I know I am in good hands. But it has nothing to do with the CSF problems so this is not the place.
Yes, you CAN get lucky and receive competent medical care by a physician who is in it because he or she has a calling. But those people are far and few between.
Thanks again and should I not hear from you, enjoy the holidays.
Kind regards,
Marie
Hey, at least your doctor was nice enough to ASK you what you would like to do as opposed to throwing you out of the office as has happened to me on numerous occasions. Four times I was asked to leave. The other times the doctors simply brushed me off by saying, "you have been dealt a bad hand" and "do not even think for a minute that our insurance system is going to pay for you to go seek the help of some miracle healer in Timbuktu" (this was in response to a question the doctor asked ME. He wanted to know if I had heard of any specialists and I said, yes. When he asked where, I mentioned Dr. Schievink in the U.S. That's when I got the lecture on miracle healers in Timbuktu!
One might say, gee, Marie, maybe it's your attitude....at this point you're d***** right it is! After what I have been through, I have developed a very low opinion of doctors in general and to even hear the word mentioned sets me off. So I had a 9-month time out, WITH therapy to try to make sense of it all. The conclusion is that it makes no sense whatsoever, but to be in a constant state of rage is not helping the situation any. I have an operation of a different nature coming up and in all fairness must say that in this case I know I am in good hands. But it has nothing to do with the CSF problems so this is not the place.
Yes, you CAN get lucky and receive competent medical care by a physician who is in it because he or she has a calling. But those people are far and few between.
Thanks again and should I not hear from you, enjoy the holidays.
Kind regards,
Marie
The Psycho Diagnosis
Submitted by Serendip Visitor (guest) on Sat, 11/26/2011 - 12:22pm.
Can someone, anyone, out there give me a plausible explanation as to why doctors will say symptoms one experiences are the result of a psychological illness if they do not have a test yet to prove something?
A person wrote recently about the strange taste and fluid loss, and was told it is all psychological. Hello! The person had brain surgery and it is VERY LIKELY that he/she truly DOES have a CSF leak!
I have gone through hell due to this not-being-believed by members of the medical profession, and not just for one illness.
And in each case, four in all, it turned out, once the illness had progressed to a certain degree, that I was right! Getting the medical documentation to "prove" I was not imagining things after all does not make up for all that agony of not having been taken seriously.
For some strange reason, if the doctors can find nothing, family and friends tend to also jump on the psycho wagon along with the doctors.
I am an intelligent (at least semi-intelligent) person, once functioning, living life to the fullest. Why on earth would I begin to suddenly start imagining things?
I am honest about this, I would truly like to hear an explanation that will help me be able to forgive all those diagnosticians who cannot simply say, "Gee, I hear you, but I cannot find anything. But with your description of things, it sure does sound like ......(fill in the blank)," not only in my case, but in everyone else's who has gone through the same torture. Yes, it is torture being told you are imagining things when they are, indeed, real. And everytime I read those words "I was told it is psychological" written by someone else, I become so livid. Something needs to be done about this as it is unacceptable.
Are there any lobbies out there for patients??!?
A person wrote recently about the strange taste and fluid loss, and was told it is all psychological. Hello! The person had brain surgery and it is VERY LIKELY that he/she truly DOES have a CSF leak!
I have gone through hell due to this not-being-believed by members of the medical profession, and not just for one illness.
And in each case, four in all, it turned out, once the illness had progressed to a certain degree, that I was right! Getting the medical documentation to "prove" I was not imagining things after all does not make up for all that agony of not having been taken seriously.
For some strange reason, if the doctors can find nothing, family and friends tend to also jump on the psycho wagon along with the doctors.
I am an intelligent (at least semi-intelligent) person, once functioning, living life to the fullest. Why on earth would I begin to suddenly start imagining things?
I am honest about this, I would truly like to hear an explanation that will help me be able to forgive all those diagnosticians who cannot simply say, "Gee, I hear you, but I cannot find anything. But with your description of things, it sure does sound like ......(fill in the blank)," not only in my case, but in everyone else's who has gone through the same torture. Yes, it is torture being told you are imagining things when they are, indeed, real. And everytime I read those words "I was told it is psychological" written by someone else, I become so livid. Something needs to be done about this as it is unacceptable.
Are there any lobbies out there for patients??!?
I agree ! Doctors should 'believe ' patients with CSF symptoms
Submitted by Serendip Visitor Kate (guest) on Fri, 03/30/2012 - 4:50am.
I couldn't agree more! I too, have had a CSF leak post sinus surgery, but AGAIN (it seems) I had to research and self-diagnose etc. and suffer for longer than was needed - but I shall not complain as mine was relatively quick after reading this forum .
It seems as though 'headaches' have such a bad stigma attached to them too!? Why is that?
Thankfully for me, I moved states in Australia and (after 4 x Emergency visits being told I'm stressed / fine /migraines etc. mind you!)
I finally got diagnosed as having an 'intermittent CSF cranial leak' by a neurologist who had 'seen it a few times before'. I mentioned I had thought that all along too! He didn't think I was mad, thankfully! Good bloke!
I find it extraordinary that Doctors would 'assume' first that patients 'fabricate' symptoms etc. I will definitely be advocating on behalf of all people with CSF leaks - (and any other debilitating illnesses) and as much as possible - educate.
I am a health professional myself so I hope I can achieve something!!? It seems that without RESEARCH no doctors will listen, but I will try! ;-)
Keep up believing your selves everyone
Take care and be positive.
I am still not 'fixed' 100% but it will be complex, I am resting more, and may take time... and fingers crossed not more sinus surgery.
THANK YOU for this forum.
Good luck to all,
Kate
It seems as though 'headaches' have such a bad stigma attached to them too!? Why is that?
Thankfully for me, I moved states in Australia and (after 4 x Emergency visits being told I'm stressed / fine /migraines etc. mind you!)
I finally got diagnosed as having an 'intermittent CSF cranial leak' by a neurologist who had 'seen it a few times before'. I mentioned I had thought that all along too! He didn't think I was mad, thankfully! Good bloke!
I find it extraordinary that Doctors would 'assume' first that patients 'fabricate' symptoms etc. I will definitely be advocating on behalf of all people with CSF leaks - (and any other debilitating illnesses) and as much as possible - educate.
I am a health professional myself so I hope I can achieve something!!? It seems that without RESEARCH no doctors will listen, but I will try! ;-)
Keep up believing your selves everyone
Take care and be positive.
I am still not 'fixed' 100% but it will be complex, I am resting more, and may take time... and fingers crossed not more sinus surgery.
THANK YOU for this forum.
Good luck to all,
Kate
Blood Patch
Submitted by Lin (guest) on Sat, 11/05/2011 - 5:31am.
Hello to everyone, sorry to hear of your suffering and I don't want to throw more complications at you but.
I have read quite a few of the comments and I have not come across anything that warns of the DANGER OF BLOOD PATCHES.
They are a primary cause of ARACHNOIDITIS.
We don't always get to choose "good or bad" sometimes it's "bad or worse" but to make the right choices for you, you need all the facts. Do a search - Blood Patch Arachnoiditis - and look for yourselves.
Lin
I have read quite a few of the comments and I have not come across anything that warns of the DANGER OF BLOOD PATCHES.
They are a primary cause of ARACHNOIDITIS.
We don't always get to choose "good or bad" sometimes it's "bad or worse" but to make the right choices for you, you need all the facts. Do a search - Blood Patch Arachnoiditis - and look for yourselves.
Lin
Blood Patch
Submitted by stephanie1980 (guest) on Thu, 10/27/2011 - 6:50am.
Long story short, I have been suffering from daily excruating headaches for 7 months now. One day I just woke up in excruating pain. I ended up at Er to Er for a period of 4 weeks. I was told I was having migraines to "it is all in my head" when they finally could not take it any longer and drove longer to another ER. after several tests they gave me a presumative diagnois at U of M ann arbor, mi of spontanous csf low volume headache. they said my MRI showed "sublte patch dural enhancement". During this time, I have had 2 blood patches and now 7 months later I just had my third two days ago. I have so much more to tell and add but since I am in so much pain and I can barley type. After EVERY blood patch my pain has INCREASED?!? the doctors are baffeled and said they have never heard of this. Has anyone had this problem? The pressure in the front of my head is sooo bad and the back of my neck is stiff. Its awful. yesterday I went to my doctor and he gave me 4 sets of injections in my head. I cant take this much longer. I empathized with anyone with a headache.
So I am suffering from low
Submitted by Ashgraff (guest) on Sun, 12/04/2011 - 10:29pm.
So I am suffering from low csf headaches. As a patient at u of m Ann arbor wonder who you see and what treatments. I have hone thru 2 patches. Now trying one more medication then a cistnogram to find the leak. My doc figured out I had pressure headaches in about 3 months but nothing works. The patches only lasr a week. Partly because of work I am sure. So any thoughts on what helps???
I am diagnosed with
Submitted by Serendip Visitor (guest) on Mon, 11/24/2014 - 8:02pm.
I am diagnosed with spontaneous intracranial hypotension (low pressure). This started with headaches in the spring and severe neck pain and stiffness, then I woke up to hearing loss in left ear and whooshing sound. After seeing an ENT he had MRI done and found menegeal enhancement. I've had 2 blood patches that only lasted a week. Since then I take amitriptyline and I am on caffeine and try to up my salt intake to retain fluid. I drink all day and have to at least have 1 Gatorade a day . Since doing this I have not had a headache or nausea in 4weeks! I've also heard to avoid heavy lifting and bending over. The caffe was the biggest help though! It's speeds production of csf
I am also at U of M and see
Submitted by stephanie1980 (guest) on Thu, 12/22/2011 - 1:54am.
I am also at U of M and see Dr. Wade Cooper. I highly recommend him. He is very attentive and compassionate. Have you gone through the cistnogram?
csf leak
Submitted by Serendip Visitor (guest) on Wed, 10/19/2011 - 1:00pm.
i have a very bad diagnosed csf leak from my right nostril, it pours out. i end up dripping fluid on everything then at times it spurts so much i end up choking.this started in august 2011.apparently there is a hole just under my pituitary gland in my skull.i have had 2 brain scans now and given numerous samples of fluid.i have just been refered to another specialist that can repair it and am waiting for an appointment.i have terrible like sea sickness and headaches.i was on complete bedrest but have given up on that now, am slowly going insane.i have done nothing that could have caused this.whats this facebook group can't find it??.am in the uk
katie
katie
Katie, Try and find Mayo
Submitted by Connie Paulak (guest) on Wed, 10/26/2011 - 5:47am.
Katie,
Try and find Mayo trained neurologist in your area, they are very good doctors. Wish you the best.
Connie
Try and find Mayo trained neurologist in your area, they are very good doctors. Wish you the best.
Connie
CSF LEAKS (Cerebrospinal Fluid Leak) & Intracranial Hypotension
Submitted by Serendip Visitor (guest) on Thu, 10/20/2011 - 6:04pm.
CSF LEAKS (Cerebrospinal Fluid Leak) & Intracranial Hypotension
If that link does not take you right to the page, when you log onto Facebook, type in CSF Leaks and that forum is the first one which will pop up.
Good luck to you.
I have not had any good luck myself, except coming out of two surgeries with no paralysis. No one here can help me. And I have given up. A person can only run against a brick wall for so long, and then one day you simply stop in your tracks, realizing it is of no use. That is where I am at now.
My life is gone, I am sick every single day, and this is how the rest of my life is going to be, I fear.
But your story will have something different about it and maybe you will be lucky and get some information which will help you.
Others have been successfully treated. It's the unsuccessful stories which stay on the forums, normally. Those who have had successful treatment are getting on with their lives.
Again, good luck in your search.
Marie
If that link does not take you right to the page, when you log onto Facebook, type in CSF Leaks and that forum is the first one which will pop up.
Good luck to you.
I have not had any good luck myself, except coming out of two surgeries with no paralysis. No one here can help me. And I have given up. A person can only run against a brick wall for so long, and then one day you simply stop in your tracks, realizing it is of no use. That is where I am at now.
My life is gone, I am sick every single day, and this is how the rest of my life is going to be, I fear.
But your story will have something different about it and maybe you will be lucky and get some information which will help you.
Others have been successfully treated. It's the unsuccessful stories which stay on the forums, normally. Those who have had successful treatment are getting on with their lives.
Again, good luck in your search.
Marie
Dear Katie - try to find the
Submitted by Tali Danenberg (guest) on Thu, 10/20/2011 - 1:42pm.
Dear Katie - try to find the facebook group:
It is very helpful
It is very helpful
Pseudo tumor cerebri
Submitted by Misty (guest) on Sat, 10/08/2011 - 9:57pm.
I was diagnosed with PTC last year.. had a spinal tap with opening pressure of around 24 I think?? I was not overweight, I was 169 at 5"1 I guess that could be considered overwieght for height and weight. Since then I have lost weight and I am now 128 pounds.. I have had a HORRIBLE headache for almost 2 weeks now.. It seems to get better when I lay down and really that is all I want to do.. I do not want to go anywhere or do anything.. This has effected my life so much and much more than I can even tell people because they do not understand. I have become very depressed with this condition as well. I am not sure if you can have a spinal leak after a years time. I was feeling alright and then just a few weeks ago the headaches came on really bad. Somedays I just feel like I am going to die, or that I want to die. It gets so unbearable at time. If anyone has thse same conditions I would love to hear from you!
CFS Leaks
Submitted by Connie Paulak (guest) on Tue, 10/04/2011 - 10:06pm.
Well it looks like we have to be our own doctors these days. What I have that I call (moments) is, head feels like it is in a vise from lower back of head over the ears through the temples to the frontal. If I move to fast with my head or step down hard it feels like my brain hits the frontal of my head. My hands and feet tingle and have numbness. My wrist and ankles (when having a bad moment) will spasm. My eyes can't focus, my abs feel like they are tight. I have to sit down to recover, can't look up. Every sound is louder in my head with my heart beat. When my feet fall asleep it takes longer for them to snap out of it. I been dealing with this for last 3 years now and have seen every doctor possible. Now I'm going back to a neurologist, for the second time. I see him at the end of the month and I've taking notes on everything my body does in these moments. I thought I had if figured out when I read the side efffects of the Genric's I take. I'm back to name brand on all except one, which I will get changed with my NEW doctor tomorrow. Do not be afraid to get a new doctor, most of them are so tapped out it's not even funny. I'll let you know what happenes when I see the neurologist. Thanks, Connie
Hey Connie, please let us
Submitted by Serendip VisitorBetty Bouchillon (guest) on Tue, 10/25/2011 - 3:21pm.
Hey Connie, please let us know what your dr said about this. My husband is dealing with something know going on 5 months. They can't find anything. He is very fatigued at all times. He sleeps all night and gets up the next day very tired. Can't find anyone here to help us. Thanks for this info.
Hello everyone, I want to
Submitted by Connie Paulak (guest) on Thu, 10/27/2011 - 10:49pm.
Hello everyone,
I want to update you on my visist to the neurologist today. I do Not have CSF leak, what a relief. The doctor said that I need more sodium in my diet and less water....that was kinda wierd?? The main thing I did was reach when I started to have my moments, that was the best thing I could have ever done. I believe my moments were contributed to taking Generic medications. I'm back to name brands and I feel great. I have lost 30 pounds and my cholesterol went down by 10 points. Yesterday I had my first day of No moments, today I had a small one and that was very mild, I couldn't look up. Please research all the life changes with meds, food, life style, it saved me. Best of luck to all of you, I will still research for people on hear that need help.
God Bless
Connie
I want to update you on my visist to the neurologist today. I do Not have CSF leak, what a relief. The doctor said that I need more sodium in my diet and less water....that was kinda wierd?? The main thing I did was reach when I started to have my moments, that was the best thing I could have ever done. I believe my moments were contributed to taking Generic medications. I'm back to name brands and I feel great. I have lost 30 pounds and my cholesterol went down by 10 points. Yesterday I had my first day of No moments, today I had a small one and that was very mild, I couldn't look up. Please research all the life changes with meds, food, life style, it saved me. Best of luck to all of you, I will still research for people on hear that need help.
God Bless
Connie
I will, thak you. How old is
Submitted by Connie Paulak (guest) on Wed, 10/26/2011 - 5:40am.
I will, thak you. How old is your husband?
Connie
Connie
Where are you located? Connie
Submitted by Connie Paulak (guest) on Tue, 10/25/2011 - 8:06pm.
Where are you located?
Connie
Connie
Advice-help-child
Submitted by Emili-RO (guest) on Sun, 10/02/2011 - 6:52pm.
I'm from Romania. I have a girl three years and 10 months old.
Last year he had meningitis. Even before the meningitis runny from nose, right nostril a liquid like tears. Only 2 weeks back, I found out that fluid is cerebrospinal fluid. Currently about 3-5ml runny every day. If someone can tell how serious it is, what to do, if you can live without surgery, which is the best doctor costs? Thank you
Last year he had meningitis. Even before the meningitis runny from nose, right nostril a liquid like tears. Only 2 weeks back, I found out that fluid is cerebrospinal fluid. Currently about 3-5ml runny every day. If someone can tell how serious it is, what to do, if you can live without surgery, which is the best doctor costs? Thank you
Advice-help-child
Submitted by Connie Paulak (guest) on Thu, 10/20/2011 - 1:28pm.
I live in USA not sure what your doctors in Romanis cost. You need to take your child to see a neurologist and geta MRI of his head and neck. He may have CSF, I would check with doctor first.
Wish you the best and your child too.
Connie
Wish you the best and your child too.
Connie
Thank you
Submitted by Emili-RO (guest) on Tue, 10/25/2011 - 3:00am.
Thank you very much! Your advice help us! Excuse my English language, because I am slovak from Roumania.
You are welcome. You might
Submitted by Connie Paulak (guest) on Wed, 10/26/2011 - 5:43am.
You are welcome. You might have Mayo Clinic trained neurologist in your area, they are very good Doctors. Have a great day.
Connie
Connie
CSF Leak Be Warned
Submitted by Johnh (guest) on Mon, 09/26/2011 - 12:54pm.
I am no doctor or have any in depth medical knowledge but would like to tell others my experience of a CSF leaks. Following a (no risk???)sinus operation i began to feel unwell and complained to hospital staff, the surgeon and a GP, none of whom would take my complaints of not feeling well seriously. Five days after the operation i was admitted to ER with symptoms of servere headache, photophobia, nausea and vomiting. My glassgow rating was 3/15. The surgeon had perforated the orbital wall leading to a cerebrospinal fuild leak. This provided entry point for meningitis bacteria which is found in the throat of any health human being. The CSF leak lead to hydrocephalus(swelling on the brain). This swelling lead to the following secondary complications; bilateral third nerve palsy(blindness), inflammatory myelitis( C5 incomplete quadriplegia),deep vein thrombosis, pulmonary embolism(blood clot on lungs) and faecel and urinary incontinence. A CT scan performed at the time failed to detect a source for the meningitis.
All this could have been avoided if the ENT surgeon had have provided me with prop-lactic antibiotics. The initial entry point for the leak healed on its own accord a few weeks after the operation. Prior to operation i was very active 32 year old male who enjoyed the outdoors.
All this could have been avoided if the ENT surgeon had have provided me with prop-lactic antibiotics. The initial entry point for the leak healed on its own accord a few weeks after the operation. Prior to operation i was very active 32 year old male who enjoyed the outdoors.
I have been suffering for
Submitted by Cheryl (guest) on Tue, 09/20/2011 - 12:03pm.
I have been suffering for nearly 4 years, been to the ER 4 times, seen two different neurologists. Always diagnosed with migraines, but I am convinced that I have a CSF leak. I have all the symptoms, even numbness in my feet and hands at times and a metallic taste in my mouth, (was told I have neuropathy)I have been seeing my primary physician nearly twice a month for the past 3 years, getting several prescriptions for migraines, but none seem to work. I am in the Kansas City area. Does anyone know of a doctor close to here that has any experience treating CSF leaks with positive results? I have been turned down at Mayo.
Any help is greatly appreciated,
Cheryl
Any help is greatly appreciated,
Cheryl
support group
Submitted by Weary Wife (guest) on Thu, 08/25/2011 - 8:03am.
found this support group for leakers created by leakers, it looks like a good place to get information!
CSF Leak
Submitted by Andrea Fulcher (guest) on Mon, 08/22/2011 - 7:58am.
In January 2011 I woke up feeling quite unwell but put it down to the after math of Xmas Celebrations. 3 days into feeling ill after vomitting, my hearing going tinny and the most horrendous headache i had ever had, i took myself to our local GP walk in centre, to be told I had a severest of migraines and given migraleve. Next day not satisfied with the diagnosis I returned to be told by a different GP that I had a Sinus infection, and given more tablets to take home. That night I went to Local hospital and although they could see how much pain I was in as I couldnt lift my head up without screaming, they sent me home saying I had a migraine. I perseverred for another week at home until the pain was unbearable. Returned to the hospital and refused to go home until they gave me some kind of scan to find out what was going on in my head. I was admitted that day and endured 7 lumber punctures, each time failing to get any fluid from my spine until the last one which had blood in it. Afterwards I was sent for a CAT Scan on my head, but unbelievable to me it all came back clear. They discharged me with painkillers, and booked me for an MRI scan later that week. After the scan I was called to see my Consultant who informed me that the scan showed a collection of small bleeds to the back of my brain, but as they weren't bleeding anymore I was sent home with stronger painkillers and told they would scan me again after a month!!!! 3 days later the pain in my head was so agonising that I took myself to a different hospital and within an hour of being there and seeing a Neurologist I was admitted and told I have SIH causing the CSF leak. At this point I couldnt walk so how I was originally sent home is beyond me. 4 days later after complete bedrest I had an epidural blood patch. two hours later I was made to get up and the ripping in my head instantly attacked again. it hadnt worked. More MRI/CAT Scans later the Docs confirmed that the tear was in my neck. I was booked in for a Myleogram and Blood Patch. Unfortunately after the myleogram they couldnt see the hole under the CT guidance so the basic epidural blood patch was given again. After a month confined to my bed I was eventually released as it seemed to be a success, although I still have never experienced a time since when I was totally headache free. A month or so ago, I started with the same symptoms again, nausea, vomitting, headaches, burning sensation in my head, neck stiffness and pain - Once in contact with the hospital again I was fastracked straight to the neurology clinic and given another blood patch, but the symptons remained and gradually worsened, leading to a second blood patch the following week. To date, the symptoms are still there but just as at the beginning and building up, and I am waiting to be seen in clinic again to see what the next stage is - dont think my body could bear another epidural blood patch as the pain afterwards was horrendous, worse than childbirth..............praying for a solution soon, as I want my life back, I am only 39 and have years left in this old dog yet lol
spontaneous csf pain relief
Submitted by pupp (guest) on Thu, 11/17/2011 - 2:45pm.
Been suffering from spontaneous csf leak since 1st april 2011. Kept being told it was tension headache or migraine but knew that it wasn't either of those as it was postural (when i was sitting up or standing)
Nothing shows on CT or MRI and I've had a caffeine infusion which didn't work either. Not keen to try blood patch as can't find site of leak(s) Seven months later and still the same.
However I have been prescribed Amatriptyline and now take 70mg per day. It doesn't take the pain away but makes it just bearable enough to get up and about for a little while every day... that and the fact i'm getting used to the constant pain.
Amatriptyline is the only pain killer which has made any difference to me.
Nothing shows on CT or MRI and I've had a caffeine infusion which didn't work either. Not keen to try blood patch as can't find site of leak(s) Seven months later and still the same.
However I have been prescribed Amatriptyline and now take 70mg per day. It doesn't take the pain away but makes it just bearable enough to get up and about for a little while every day... that and the fact i'm getting used to the constant pain.
Amatriptyline is the only pain killer which has made any difference to me.
Try the Blood Patch
Submitted by Serendip Visitor (guest) on Fri, 11/18/2011 - 3:03pm.
I experienced a CSF Leak in January 2011. They did multiple MRI/CT and never found the hole. On February 9th they went ahead with the blood patch. It took a few days but my spine started filling up with fluid and 3 weeks later I was back to normal. I highly suggest you do the blood patch. You won't know until you try it. Good luck!
blood patch
Submitted by pupp (guest) on Fri, 12/09/2011 - 6:06pm.
Both my neurologist and consultant anaesthetist (he'd do the patch) have said a blood patch within a few weeks of it starting would have beast chance of working and that if I had been diagnosed sooner then a blood patch would be a good idea. (It took 4 months and lots of fighting from me to confirm it was SIH and it's now 8 months since the day it started) Both say that it's not very likely to help due to 1: not finding site of leak(s) 2: it's now 8 months after it started. I've been told to increase my dose of amitriptyline from 70mg to 100mg per day but i haven't found any difference in pain felief so far.
I have been able to get back to work which has really helped me keep sane. However i have to work reduced hours and also take time off every few weeks. But it's very difficult and at the moment I'm really struggling because i'm exhausted, tearful and feel hopeless. Not to mention still being in constant pain.
I'm usually in bed around 8pm (staying up late tonight but i know i'll suffer for it during the next couple of days)
I have found that keeping well hydrated, eating small & often and lots & lots of coffee helps but lying out flat is definitely the best relief.
I hate the thought that I could be like this forever so I'm still fighting to resolve this.
I have been able to get back to work which has really helped me keep sane. However i have to work reduced hours and also take time off every few weeks. But it's very difficult and at the moment I'm really struggling because i'm exhausted, tearful and feel hopeless. Not to mention still being in constant pain.
I'm usually in bed around 8pm (staying up late tonight but i know i'll suffer for it during the next couple of days)
I have found that keeping well hydrated, eating small & often and lots & lots of coffee helps but lying out flat is definitely the best relief.
I hate the thought that I could be like this forever so I'm still fighting to resolve this.
Medical Support
Submitted by Serendip Visitor (guest) on Sat, 12/10/2011 - 6:47pm.
How had those of you out there with relatively quick diagnoses been able to find a competent neurologist who would take an interest?
I suffered symptoms for 8 years until during an exploratory mastoidectomy my osteodura defect was discovered. As the doctor admittedly had not expected that (although you could see it on all the diagnostic pictures, if you ask me!), his repair job failed. Four weeks later I was in again for emergency surgery, repair job failed again.
Now I have to live with this. I am in bed 22, sometimes even 23 hrs. out of 24. Some days I push it to keep my sanity and do something upright which then causes that horrible pressure at the base of the skull behind the ear where the defect is and I get pains and a very strong pulling sensation behind my eyes. So much for the update on what my story is (have written the long version already ages ago on this site).
My problem is, despite the two failed surgeries (csf fluid leakage through the ear tube, now through the nose, confirmed by the lab, current mri and ct scans show the defects are still there, even larger than before the first surgery because during the two surgeries the edges of the holes were "smoothed over," I cannot get a doctor--anywhere here in Munich--to confirm that I indeed am suffering these symptoms! I am, by the most, still being told they know nothing about such defects, do not have time to "read up on it" and that what I am experiencing is most likely psychological.
I cried, kicked and screamed about that for a looooong time, now I can only say to myself "what jerks" they all are for treating me this way.
I need a doctor who will take me seriously, take the time to "look it up" and confirm that what I am going through on a daily basis is indeed the consequence of me having a 3 cm gaping hole in the dura and skull base. I also have a brain prolapse. During each surgery a part of the brain which inevitably falls through that hole was surgically removed, but as the hole is still there, the brain still shifts down through that hole (a 3 cm small part).
Even the surgeon who operated on me, and knows and confirmed in writing that the surgeries did not work refuses to give me any support concerning a confirmation of my symptoms resulting from that defect. He, too, said that he cannot rule out that my symptoms are not psychological. He told me in the presence of a friend that most likely what they see in the latest mri and ct scan images is the prolapsed brain, collection of csf, but that it cannot be said for sure. It could also be "inflamed mastoid cells."
Why are they acting like this? I need this diagnosis and the consequences thereof confirmed in writing in order to get the help I need on a daily basis. I am no longer aber to do things like bend over to clean a bathtub, do grocery shopping, change my bedding. I wait for help to stop by, friends whenever they can "fit me in" and I do not understand why in the U.S. so many of you with even smaller leaks which do not even show up on the images, were able to get diagnosed in under a year, and are being taken seriously.
Why are the doctors I have heard about so often here and on Facebook willing to "look it up," whereas here I have been told repeatedly by so many doctors I have consulted that they know nothing about the illness and have no time to be reading up on it, that I am simply out of luck?
Why am I not getting confirmation of this from the very surgeon who knows because he is the one who pulverized away parts of my skull go "get a good look" and did not replace that bone so now that ear is sunken into the skull on the side where a healthy person has the mastoid part of the skull to support the ear (the ear tube is squished flat causing me to be hard of hearing on that side)?
These are not rhetorical questions. I am trying to make sense of this without going mad. My guess is that doctors here in Germany are not held accountable for their actions. Under law they are allowed to misdiagnose and make mistakes. I have been told this. Also, I think that my surgeon who performed the two mastoidectomies is perhaps afraid to "got out on a limb" for me is afraid it will reflect negatively upon him?
The surgeon told me he has no way of knowing what I am going through, therefore he cannot confirm it. Also, there are not sufficient studies on this illness, he added.
This forum for me is about remaining sane. It is the only place where I can find people who know what I am going through symptom-wise which itself takes a load off. But the rest of my questions.....I cannot make any sense of it and I find it downright cruel.
Are there any members of the medical profession on this forum who might help me to be able to understand the treatment I am getting?
I thought initially, it must "be me." I have tried remaining stone-faced and matter-of-fact, I have tried the friendly approach, I have cried, have become hysterical even twice, I have tried everything, and no matter how I present my case, I get the same response. Two doctors actually told me never to come back.
I contacted the insurance company, who suggests the GP get things rolling, only to have the GP flip out completely and say (more or less, it was in German): "Am I the idiot around here? Oh, just come to Dr. _________, he's so stupid, he'll do anything."
The other GP said, it does not matter what you do, it will all be an experimenting around, and your symptoms are most likely psychological anyway.
Another GP said: "I am not even going to touch that subject! I know nothing about it and I wipe my hands of it. You must look for someone else."
I could go on and on because it has been years of this living hell, but now I must find peace and come to terms with the fact that I do not have access to any doctors "who get it" in the U.S. I live here and the system is not going to pay for me to go abroad to get an operation. I have been told this by the one neurologist I consulted who studied at Harvard and was able to explain what is going on in the brain (the pulling behind the eyes, etc.) that the German system is not going to send me to Timbuktu just because there is someone there who claims to be a miracle healer. He actually said that because I had mentioned a specialist, Dr. Schievink, in California.
And although this Harvard-educated neurologist was able to explain things about my illness, he refused to write the doctor's report required by the GP who sent me to him.
I must stop here as I doubt most have the time or energy to read through all of this.
But please, I am looking for answers as to why I am getting this treatment. I honestly do not understand and I am starting to cry again, so it is time to stop writing about it.
Any members of the medical profession with an insight, please write in.
Thanks and a good luck to everyone.
Marie
So
I suffered symptoms for 8 years until during an exploratory mastoidectomy my osteodura defect was discovered. As the doctor admittedly had not expected that (although you could see it on all the diagnostic pictures, if you ask me!), his repair job failed. Four weeks later I was in again for emergency surgery, repair job failed again.
Now I have to live with this. I am in bed 22, sometimes even 23 hrs. out of 24. Some days I push it to keep my sanity and do something upright which then causes that horrible pressure at the base of the skull behind the ear where the defect is and I get pains and a very strong pulling sensation behind my eyes. So much for the update on what my story is (have written the long version already ages ago on this site).
My problem is, despite the two failed surgeries (csf fluid leakage through the ear tube, now through the nose, confirmed by the lab, current mri and ct scans show the defects are still there, even larger than before the first surgery because during the two surgeries the edges of the holes were "smoothed over," I cannot get a doctor--anywhere here in Munich--to confirm that I indeed am suffering these symptoms! I am, by the most, still being told they know nothing about such defects, do not have time to "read up on it" and that what I am experiencing is most likely psychological.
I cried, kicked and screamed about that for a looooong time, now I can only say to myself "what jerks" they all are for treating me this way.
I need a doctor who will take me seriously, take the time to "look it up" and confirm that what I am going through on a daily basis is indeed the consequence of me having a 3 cm gaping hole in the dura and skull base. I also have a brain prolapse. During each surgery a part of the brain which inevitably falls through that hole was surgically removed, but as the hole is still there, the brain still shifts down through that hole (a 3 cm small part).
Even the surgeon who operated on me, and knows and confirmed in writing that the surgeries did not work refuses to give me any support concerning a confirmation of my symptoms resulting from that defect. He, too, said that he cannot rule out that my symptoms are not psychological. He told me in the presence of a friend that most likely what they see in the latest mri and ct scan images is the prolapsed brain, collection of csf, but that it cannot be said for sure. It could also be "inflamed mastoid cells."
Why are they acting like this? I need this diagnosis and the consequences thereof confirmed in writing in order to get the help I need on a daily basis. I am no longer aber to do things like bend over to clean a bathtub, do grocery shopping, change my bedding. I wait for help to stop by, friends whenever they can "fit me in" and I do not understand why in the U.S. so many of you with even smaller leaks which do not even show up on the images, were able to get diagnosed in under a year, and are being taken seriously.
Why are the doctors I have heard about so often here and on Facebook willing to "look it up," whereas here I have been told repeatedly by so many doctors I have consulted that they know nothing about the illness and have no time to be reading up on it, that I am simply out of luck?
Why am I not getting confirmation of this from the very surgeon who knows because he is the one who pulverized away parts of my skull go "get a good look" and did not replace that bone so now that ear is sunken into the skull on the side where a healthy person has the mastoid part of the skull to support the ear (the ear tube is squished flat causing me to be hard of hearing on that side)?
These are not rhetorical questions. I am trying to make sense of this without going mad. My guess is that doctors here in Germany are not held accountable for their actions. Under law they are allowed to misdiagnose and make mistakes. I have been told this. Also, I think that my surgeon who performed the two mastoidectomies is perhaps afraid to "got out on a limb" for me is afraid it will reflect negatively upon him?
The surgeon told me he has no way of knowing what I am going through, therefore he cannot confirm it. Also, there are not sufficient studies on this illness, he added.
This forum for me is about remaining sane. It is the only place where I can find people who know what I am going through symptom-wise which itself takes a load off. But the rest of my questions.....I cannot make any sense of it and I find it downright cruel.
Are there any members of the medical profession on this forum who might help me to be able to understand the treatment I am getting?
I thought initially, it must "be me." I have tried remaining stone-faced and matter-of-fact, I have tried the friendly approach, I have cried, have become hysterical even twice, I have tried everything, and no matter how I present my case, I get the same response. Two doctors actually told me never to come back.
I contacted the insurance company, who suggests the GP get things rolling, only to have the GP flip out completely and say (more or less, it was in German): "Am I the idiot around here? Oh, just come to Dr. _________, he's so stupid, he'll do anything."
The other GP said, it does not matter what you do, it will all be an experimenting around, and your symptoms are most likely psychological anyway.
Another GP said: "I am not even going to touch that subject! I know nothing about it and I wipe my hands of it. You must look for someone else."
I could go on and on because it has been years of this living hell, but now I must find peace and come to terms with the fact that I do not have access to any doctors "who get it" in the U.S. I live here and the system is not going to pay for me to go abroad to get an operation. I have been told this by the one neurologist I consulted who studied at Harvard and was able to explain what is going on in the brain (the pulling behind the eyes, etc.) that the German system is not going to send me to Timbuktu just because there is someone there who claims to be a miracle healer. He actually said that because I had mentioned a specialist, Dr. Schievink, in California.
And although this Harvard-educated neurologist was able to explain things about my illness, he refused to write the doctor's report required by the GP who sent me to him.
I must stop here as I doubt most have the time or energy to read through all of this.
But please, I am looking for answers as to why I am getting this treatment. I honestly do not understand and I am starting to cry again, so it is time to stop writing about it.
Any members of the medical profession with an insight, please write in.
Thanks and a good luck to everyone.
Marie
So
CSF Leak
Submitted by Serendip Visitor (guest) on Sat, 04/12/2014 - 3:53am.
HI Marie, I just read your article/posting...did you ever find relief? did you end up going to see Dr. Schievink? If so what happened?
My husband is currently going through a untraceable CSF leak and he is suffering.
Thank you and I look forward to hearing back from you
Kendra
My husband is currently going through a untraceable CSF leak and he is suffering.
Thank you and I look forward to hearing back from you
Kendra
CSF leak
Submitted by Stephanie Fitton (guest) on Sun, 09/11/2011 - 11:56pm.
I came upon your post while doing research. My situation is very simular to yours. It started in February 2011 and I am still sick daily. I just turned 28 years old and there is no known cause for my CSF leak. I have undergone 5 blood patches at different locations in my spine, and none have worked. My leak is too small to be seen on a scan (it always has been) so the doctors are not sure what else to try. Im sick daily and spend alot of time just hoping I will wake up one day and it will be gone. I go for my 6th blood patch next month and just the thought of undergoing that pain yet again makes me feel more sick. It was good that I happened by your post because I really feel totally alone in all of this because my doctor said its very rare so there isnt even much research to go on, nevermind other people who understand what im going through. If you want to compare stories or just have someone to talk to who knows how you feel, send me and email at . Thanks, Stephanie
CSF Leak
Submitted by Andrea Fulcher (guest) on Tue, 09/27/2011 - 5:58am.
Hi Stephanie,
Just read your comments on here. Like you, there is no known reason what caused my CSF Leak, and after 4 blood patches now, I am waiting to see my Doctor again as the symptoms once again have reared their ugly head - burning headaches, horrendous neck stiffness - there's got to be more to life than feeling yukky like this all the time. I too have had another MRI scan on my neck and spine and this time they were unable to locate the leak on the scan - but i was told that sometimes the scan is not reliable in these instances as they can be so hard to detect - unless yr totally gushing when losing your fluid......i know exactly how you are feeling, about being alone - as its such a rare thing, when you talk to people about it, they dont understand, and sometimes wonder if they realise what a painful and awful thing it is to have to go through. I have today found the Facebook that has a forum on it, if you would like to join and we can compare notes on that, just put CSF Leak in the search engine and it will direct you to their page. Hope you are feeling better soon.
Just read your comments on here. Like you, there is no known reason what caused my CSF Leak, and after 4 blood patches now, I am waiting to see my Doctor again as the symptoms once again have reared their ugly head - burning headaches, horrendous neck stiffness - there's got to be more to life than feeling yukky like this all the time. I too have had another MRI scan on my neck and spine and this time they were unable to locate the leak on the scan - but i was told that sometimes the scan is not reliable in these instances as they can be so hard to detect - unless yr totally gushing when losing your fluid......i know exactly how you are feeling, about being alone - as its such a rare thing, when you talk to people about it, they dont understand, and sometimes wonder if they realise what a painful and awful thing it is to have to go through. I have today found the Facebook that has a forum on it, if you would like to join and we can compare notes on that, just put CSF Leak in the search engine and it will direct you to their page. Hope you are feeling better soon.
Hi Stephanie, I was diagnosed
Submitted by Tali Danenberg (guest) on Mon, 09/12/2011 - 4:02pm.
Hi Stephanie,
I was diagnosed with this spontanous CSF leak since mid August. I still have pain but it seems to be of a differnet nature. I rest most of the day so I'm noit sure it's th esame pain or some other headache nerve pain. Do you rest / lie down all day?
I was diagnosed with this spontanous CSF leak since mid August. I still have pain but it seems to be of a differnet nature. I rest most of the day so I'm noit sure it's th esame pain or some other headache nerve pain. Do you rest / lie down all day?
would like to consult
Submitted by Tali Danenberg (guest) on Sun, 09/04/2011 - 2:54pm.
Would be happy if you can send me you phone number including country and area code as I'm suffering from the same symptoms
do not know if you meant me but here it is
Submitted by Serendip Visitor (guest) on Fri, 09/23/2011 - 2:44pm.
i have a flat rate for the us and for all of central europe so i can call you back for free, if i am the person you meant.
for some reason the facebook connection did not show up properly on the page as far as i could tell so here it is again:
once you get into facebook.com you have to type in csf leaks under groups. this will lead you to the forum within which are several different discussion subjects, all ending as one big one if you ask me.....not very helpful, but at least you will not be alone. i have not found any real answers there than can help me. i am very ill, with two failed mini-craniotomies under my belt am pretty negative these days. am angry at the world and especially at all the doctors who did not take me seriously, who gave me the psycho-stamp on my forhead instead of believing me. i am not angry for getting sick as there is no right to health. also i am not angry at not having been healed. i AM angry, very angry, for having been lied to, not taken seriously (THAT issue again), and having been left alone with this problem by the doctors. not one single doctor is willing to help me find competent treatment here in europe, let alone in the u.s. or anywhere else. alone i am getting nowhere and have given up for the time being. the issue has been put on the back burner where it is going to stay until i either croak, or somehow manage to muster up a new wave of energy to go at it again.
if things are so complicated, and the hurdles are so high, it is not worth it in the end. which is why--for now--i have given up.
hope you have a better journey.
for some reason the facebook connection did not show up properly on the page as far as i could tell so here it is again:
once you get into facebook.com you have to type in csf leaks under groups. this will lead you to the forum within which are several different discussion subjects, all ending as one big one if you ask me.....not very helpful, but at least you will not be alone. i have not found any real answers there than can help me. i am very ill, with two failed mini-craniotomies under my belt am pretty negative these days. am angry at the world and especially at all the doctors who did not take me seriously, who gave me the psycho-stamp on my forhead instead of believing me. i am not angry for getting sick as there is no right to health. also i am not angry at not having been healed. i AM angry, very angry, for having been lied to, not taken seriously (THAT issue again), and having been left alone with this problem by the doctors. not one single doctor is willing to help me find competent treatment here in europe, let alone in the u.s. or anywhere else. alone i am getting nowhere and have given up for the time being. the issue has been put on the back burner where it is going to stay until i either croak, or somehow manage to muster up a new wave of energy to go at it again.
if things are so complicated, and the hurdles are so high, it is not worth it in the end. which is why--for now--i have given up.
hope you have a better journey.
thank you so much. I suceeded
Submitted by Tali Danenberg (guest) on Sun, 09/25/2011 - 3:57am.
thank you so much. I suceeded to enter the facebook forum
There are several docs who do
Submitted by Traci Irving (guest) on Wed, 08/24/2011 - 7:24pm.
There are several docs who do get this if you can get to them..and travel..I know your dilemma...wouter schievik at cedars sinai in la...linda gray at duke unversity...jawad shah at iinn.com in michigan..they are the best so far we have a page on facebook for support and answers.. mayo clinic in arizona..minnesota...dr mokri...good luck
what is the facebook
Submitted by Tali Danenberg (guest) on Mon, 09/12/2011 - 4:15pm.
what is the facebook connection? can't find it.
blood patches??
Submitted by Serendip Visitor (guest) on Tue, 08/23/2011 - 11:52am.
Hi, I suffer from spontaneous csf leakage, the meaning of which is clearly explained at the beginning of this forum: hole in the dura for no apparent reason, erosion of the bone at the skull base, brain prolapse and persistent liquorrhoe.
I request for all comments to be sent to me because I never know when maybe, just maybe there will be a tidbit of information which will help me. I have had two failed surgeries, a long history of false diagnoses and not being believed, being called lazy, it's "all in your head" (hey, but it really IS all in my head!), and even now that the surgeon saw for himself, something which he admitted he had never encountered before in his professional life (which might possibly be the reason why both surgeries failed???), he does not have anyone to compare me to and does not believe that even though all the above has been confirmed, what it feels like to have these problems with the accompanying symptoms everyone knows about (dizziness, pressure, pain, nausea, fatigue), he does not believe they stem from my problem. I am still after all I have been through being told it is psychological.
Well, now my psychological state after years of this, having lost my life, no longer able to work, cannot even keep up a normal social life because I have to lie down so often, I really am depressed and ask myself repeatedly, why DO I hang on to life in this state when there is basically nothing left except the bed I lie in almost 24/7. Surrounded by so many people ignorant of the illness, I have lost friends because they just don't get it and are not willing to truly get informed.
But to get to my point: Please, fellow sufferers, what is this with the blood patches? I still do not understand why they are used and what symptom they are supposed to alleviate. Do you also suffer from a hole in the dura and skull base? Or is your illness something completely different, but with the same symptoms associated with losing CSF?
I keep reading entries, those affected understand each other, but I have never heard of having a blood patch before entering this site with my problem as the title of the site is the description of my problem. But there are so many people who talk of the blood patches....
Would like to get informed as I wonder if this is a type of therapy? And if so, does it work? And for whom is it suited?
I have been told to my face here in Germany, I am out of luck. I need THE expert surgeon who has successfully performed the operation at least 25 times and I have been dealt a poor hand. It is my own tough luck. All the other doctors I have seen did not even take the time to look the illness up. I have been thrown out of doctors' offices with my problem. They shrug their shoulders, say they have never heard of such a thing, and I am on my own.
But I am not on my own as there quite obviously others who have had the same horrible experience. However, some have found healing. I do not have access to the experts in the U.S. for insurance reasons. I had sent all my records to Johns Hopkins and a year later was asked to come in for a visit! How on earth can I travel alone to the U.S. when I cannot even sit upright for longer than a few hours? And who is going to pay for it? I am penniless as I can no longer work. Life really is bleak now. And the worse part is, there is no end in sight. I could go on living like this for another 30 years. So I ask myself repeatedly, just what it is holding me back from taking the proper action to end it. I have no quality of life left.
I am very, very sad, and hopeless.
I request for all comments to be sent to me because I never know when maybe, just maybe there will be a tidbit of information which will help me. I have had two failed surgeries, a long history of false diagnoses and not being believed, being called lazy, it's "all in your head" (hey, but it really IS all in my head!), and even now that the surgeon saw for himself, something which he admitted he had never encountered before in his professional life (which might possibly be the reason why both surgeries failed???), he does not have anyone to compare me to and does not believe that even though all the above has been confirmed, what it feels like to have these problems with the accompanying symptoms everyone knows about (dizziness, pressure, pain, nausea, fatigue), he does not believe they stem from my problem. I am still after all I have been through being told it is psychological.
Well, now my psychological state after years of this, having lost my life, no longer able to work, cannot even keep up a normal social life because I have to lie down so often, I really am depressed and ask myself repeatedly, why DO I hang on to life in this state when there is basically nothing left except the bed I lie in almost 24/7. Surrounded by so many people ignorant of the illness, I have lost friends because they just don't get it and are not willing to truly get informed.
But to get to my point: Please, fellow sufferers, what is this with the blood patches? I still do not understand why they are used and what symptom they are supposed to alleviate. Do you also suffer from a hole in the dura and skull base? Or is your illness something completely different, but with the same symptoms associated with losing CSF?
I keep reading entries, those affected understand each other, but I have never heard of having a blood patch before entering this site with my problem as the title of the site is the description of my problem. But there are so many people who talk of the blood patches....
Would like to get informed as I wonder if this is a type of therapy? And if so, does it work? And for whom is it suited?
I have been told to my face here in Germany, I am out of luck. I need THE expert surgeon who has successfully performed the operation at least 25 times and I have been dealt a poor hand. It is my own tough luck. All the other doctors I have seen did not even take the time to look the illness up. I have been thrown out of doctors' offices with my problem. They shrug their shoulders, say they have never heard of such a thing, and I am on my own.
But I am not on my own as there quite obviously others who have had the same horrible experience. However, some have found healing. I do not have access to the experts in the U.S. for insurance reasons. I had sent all my records to Johns Hopkins and a year later was asked to come in for a visit! How on earth can I travel alone to the U.S. when I cannot even sit upright for longer than a few hours? And who is going to pay for it? I am penniless as I can no longer work. Life really is bleak now. And the worse part is, there is no end in sight. I could go on living like this for another 30 years. So I ask myself repeatedly, just what it is holding me back from taking the proper action to end it. I have no quality of life left.
I am very, very sad, and hopeless.
Don't give up!
Submitted by Serendip Visitor (guest) on Fri, 01/18/2013 - 6:52pm.
I hope this message finds you well. I felt a stong need to reply to your post. I too have a csf leak and am in bed 24/7. Unable to do anything except eat, use the bathroom, and shower. There are options to fix it. Blood patches sometimes work. It's where they inject some of your own blood into the space surrounding the membrane that holds your spinal cord. If that doesn't work they can inject a glue into the location of the leak. I'm in the middle of determine the right corse of treatment. I know you are having a hard time getting the help and treatment you need but maybe you could get in touch with a dr in Germany or the us that will help you for free. I've found a doctor in San Francisco California that has agreed to look at my scans for free. His name is William Dillon. Dr Keith Black is a neurosurgeon at cedar senai in California that will look at your scans for $50. I bet if you call and tell them your situation he may look at your info for free. At least they could confirm it and relay the message to a doctor there in Germany. I know it's exhausting dealing with everything when it takes all you have just to sit up and eat, but even going through it all I still believe everything happens for a reason. This will make you stronger... Hang in there and bug doctors until someone agrees to help you. It's your life! Fight for it!
csf leak in head
Submitted by Traci Irving (guest) on Wed, 08/24/2011 - 7:18pm.
blood patch will not work for leak in head..sorry...only surgery can repair...did they find leak location? I understand your saga..I really do..took years to find the answer..turned away so many times..told I was crazy..dye test no show leak...found new skull based nuero who finally got it...had bifrontal craniotomy to repair defect in cribriform plate with defect running into sphenoid sinus...test that discovered the leak was called intrthecal high pressure cisternagram (spell)..very invasive but no choice..had to repair anyway so why not find exact location to make sure it gets repaired correctly sure dont wanna do it again...such a very long complicated story..so I do understand your mental well being...I was THERE !!! ask anything you need..I am here to answer
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