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Arnold Chiari Malformation Support Group
A community of patients, family members and friends dedicated to dealing with Arnold Chiari Malformation, together.
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04/03/2009 05:01 PM
likaloha
Posts: 10
Member

hi there...

I would just like to quickly introduce myself and say Hi!! to everyone..I am 47 y.o. with several medical problems, but probably the most painful is the Chiari... I don't know if this is typical, but my doc didn't initially find my Chiaris, I had to ask for the specific testing to see if I had it...it was suggested to me by a colleague who's daughter had just been diagnosed... I have read some stuff about this, but as I have other disabling conditions along with this, I haven't had any treatment.. or a good neuro either... I look forward to getting to know others who have the same issues that I have, 'cuz I think that it is hard for others to really understand..Lisa

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04/05/2009 04:30 PM  Top
prism
prism
 
Posts: 66
Member

Hi Lisa,

It is very hard to get treatment for Chiari depending on how much herniation you have going on- I for one, have had no help except from the people at the Chiari Institute in NY> it depends on how much it's disrupting your life- whether it's worth it to go there or not, for me, it was really worth it.

I hope you get the help you need soon.

hugs,

zoe


04/08/2009 09:28 AM  Top
likaloha
Posts: 10
Member

Zoe.. thanks for the reply.. I live in Ohio, so going to NY now for tratment is not possible.. may research closer alternatives.. take care..Lisa

Previous discussions I participated in:
west nile virus?
hello there..
hi there...
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