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#1 | ||
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Junior Member
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#2 | ||
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New Member
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In the uk...operating on the brain doesnt seem to be a popular option unless life threatening, its so frustrating thanks everyone |
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#3 | ||
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Junior Member
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I have the same problem. My ventricles are enlarged and the symptoms all started at once. After having a cisternogram done, they said there was no blockage or leak. They said I would have to live with it. They said I was probably born with it.. So I dont know what to do now. Also they found a clover leaf aneurysm on my basilar top artery measuring 8.5 and cant do surgery on it either, because it has 5 other arteries feeding into it. To dangerous to operate. One doctor told me i'm screwed..(JERK). I know how you feel and I'll keep you in my thoughts and prayers. Cheri ![]() |
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#4 | ||
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Junior Member
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I was diagnosed at 2 mo of age with a Dandy-Walker cyst in my 4th ventricle which led to hydrocephalus. I had my first shunt at 2 mo of age, my second at 11 mo, my third at 5 yrs, and then didn't need to be shunted again until I was 32. My first adult experience of hydrocephalus was scary, vomiting, gait, bad headaches, and I received my first adult shunt tap Halloween 2003 and was hospitalized over then next 4 days for a shunt revision. Since then, 2006 and 2009 have been hard on me surgically, as now I face sharp pains in my forehead and back of neck that are not migraine in nature at all. I have had 6 shunt adjustments in 5 weeks, 3 head CT's, and 2 head X-rays. I got my first shunt tap since my last hospitalization last July. I hope my surgeon can find out how to "fine tune" my shunt valve to the right setting, because my original setting at 12 showed overdrainage. I have been set at 15, 18,
20, 16, and now 14 to see if the pain will go away on its own. I'm getting another head CT on Thursday, and I hope it can show something that these past 5 weeks of agony could not. ![]() |
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#5 | ||
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New Member
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no enlarged thymus gland | Myasthenia Gravis |