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#11 | ||
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New Member
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#12 | ||
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New Member
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Hello all. I have had a chronic CSF leak for over 16 years. Have rips in my sheniod sinus. I have had 3 unsuccessful transnasal endoscopic surgeries to try and repair.
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#13 | ||
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New Member
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I cant believe there are so many people living with this condition for years. I am convinced I have a CSF leak since a craniotomy to remove a benign brain tumour in March. Neurologists agree but no-one seems to be able to actually find anything. Have been referred to an Ear Nose and Throat consultant now - is that usual? Am lying in bed today having felt really dizzy for the past 3 days. My main worry of course is contracting meningitis - at least knowing there are so many people living with this for years means there is a chance I wont get it. Does anyone know the statistics for contracting meningitis with a CSF leak?
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#14 | ||
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Junior Member
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Had my surgery four days ago. Everything went fine, they patched the dura and I felt great for 3 days. But today I woke up with the familiar ringing in the ears. Don't really know what to do: should I call the surgeon and go back to hospital? Or should I stay in bed? I will see him next week to have the staples out. I am trying to find something to help dura heal. Does caffeine help? What about enzymes? Wobenzym or vitalzym. Did you try them?
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#15 | ||
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Junior Member
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Caffeine? Doesn't make a difference to me... Lifting things? Sometimes, it just doesn't matter, you're gonna get the leak no matter what you do. I earned a couple of leaks after a stepped down funny off of a ladder one day. |
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#16 | ||
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Junior Member
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Well, on Friday I'll have the stitches out and will see what my doc has to say. I have an MRI scheduled in a month... Ringing in the head is pretty strong.... |
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#17 | ||
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Junior Member
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Yes, I hear you ringing too ![]() |
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#18 | ||
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New Member
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My story differs slightly from what's already been posted. I too had an initial "migraines" diagnosis, but in 2009 Dr. Linda Gray at Duke UMC ( u can call DUke directly at 919 684 8111 and book an appt with Dr. Gray )found 7 tears in my dura were causing the low pressure pain. Took 14 blood patching procedures over 1 1/2 years to seal me up. Then the real culprit, HIGH pressure and underabsorption by brain tissue, was discovered. Pseudotumor cerebri is the name of the condition. It's rare but not unheard of, and in APril 2011 Dr. Gerry Grant, Duke neurosurgeon, put in a VP shunt. After initial complications (infections and then blockage) I have had good results and relief with my Codman programmable VP shunt.... until this week. Pain in my chest, along tubing route sent me to ER. no infection found in blood and no fever. was sent home with pain med Rx. I am now in contact with both doctors mentioned above (both are away at conferences, but emailing and/or calling me) to determine next step. I cannot recommend these two doctors highly enough. DOn't stop til you get to see them.
Has anyone else had chest pain from shunt catheter? It's different from infection or blockage pain. |
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#19 | ||
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Junior Member
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I don't know if you've experienced these kinds of headaches but it's the worst headache I've ever had -- it's 100X worse than the morning after way too much cheap tequila - really REALLY BAD -[/QUOTE]
Yes, I had those headaches after my first surgery in 2010. That is something hard to describe, one needs to have those to understand how bad that can be. I couldn't lift, the pain on the back of the neck was killing me. The headache would go away after I lied down. So I stayed in bed for 3 days and it went away but the leak didn't stop. We realized that much later. I was having all kinds of sensations in my head (ringing, pressure in my temples, in my ears). Now, after the second surgery (to fix the leak), I never had those headaches but I have ringing... which might be a sign of a leak. I don't want to have an MRI right away. What for? Another surgery? I will have MRI done in 3-4 months and then will go from there... It's been 15 days after the surgery. I'm going back to work next week. |
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#20 | ||
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New Member
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I have had two spinal taps and four blood patches and still have not been fixed. I have been down (90% bedridden) for over 5 months. After every blood patch I feel better for about two weeks, with only slight discomfort, and then it gets worse. I have had a billion MRI's, CT scans, CT Myelogram, etc. and they can't find the leak. My last blood patch we drove & took a train 3,000 miles so that I could lay flat to see Dr. Schievink. He did a full volume blood patch. When we left LA I felt good, but within a few days started feeling bad again. This time with even greater pain in my lower back. He came highly recommended, but I would have to say that he has been hard to reach to get answers. I don't know where to turn from here....
sleepless in st. pete |
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