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Henry
(years diagnosed)

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her brother has one too
.
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Katie D (6)



                        100+ other people know it's not "all in your head" Please join me in keeping it real.

My husband Henry Stanton and I live in the UK and have been seeing neurosurgeons in this country over the last couple of years but I am not satisfied I am getting answers and getting increasingly worried.

Henry was born with an Arachnoid cyst to his brain (LEFT SIDE) - he used to be a racing driver and following some accidents about 12 years ago he had concussion and the cyst was operated on - they wanted to put a shunt in but couldn't because the fluid was too thick so they manually drained it. He did not have any symptoms for years but in the last 2 years he has suffered from sometimes disabilitating symptoms such as acute tiredness , numbness on the left side of his brain and feeling of passing out followed by rest/sleep

When he sees the doctors and has had CAT scan earlier this year they said he is not having pressure headaches - well, he knows that as he knows how to compare from the headaches he had experienced prior to the operation but he nonetheless has got symptoms and they are not only scary but are preventing him from living normally at times.

I really want some answers - want to know whether these symptoms are at all recognized - I want to have opinions expressed as to what the causes could be or what can be done to help this

I hate the fact that nothing is suggested/done

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Join us at arachnoidcyst.net so others can feel your pain and we can get "them" to listent to us~

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Some people just send snippets so I put them all together here.

You can help the most by adding your story to arachnoidcyst.net

The Arachnoid Cyst Foundation
c/o Catherine Clay
PO Box 66820
Los Angeles, Ca 90066
1-(800)-493-5022
11am-10pm PST Weekdays

PLEASE REALIZE THE TIME DIFFERENCE
Please read through this site before calling as your answers very well could be here already.
No we do not have printed materials, you will have to print out this site.
Amy and Catherine are giving telephone suppport at this time. Amy for emotional support and Catherine for MRIs.
If you didn't find the info you need on this site or arachonidcyst.net please do call.
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This site was designed and is maintained by Miss Catherine Clay She has recently had a child and is not the best communicator at this time. Please be patient and call or e-mail back!