New Cadisal Member
 

Hi--I am a 46 year old woman with a Cadisal diagnosis (my only sibling, sister, also has been diagnosed with Cadisal). For 4 years, I was diagnosed with MS and did shots of Rebif 3 times a week. I feel that being in Atlanta I have seen the best doctors at Emory but unfortunately none are very experienced with Cadisal so help me!

I am sorry to hear about your Dx of cadasil. I found out when the Univ of Maryland Brain Bank did an autopsy on my mother. The geneticists at OHSU in Portland then concluded that I and my brother had a variant of Cadasil. The genetic lab at the U of Wash came to the same conclusion. My brother I then sent our medical info to NIH, and they agreed..so I accepted the Dx, however, my current neurologist does not. She says I show no signs of stroke and I do not have migranes, so she thinks it is some other type of leukodystrophy. My brother has an appointment in Jan with a supposed Cadasil expert at the Mayo Clinic, and I am anxious to hear what he learns.
Since the DNA test for Cadsail is not covered by medicare I decided not to pay. I had other things to spend the money on. Have you had the test?
How did they determine that you have cadasil?
Good luck to you.
"Together we have hope" is a website devoted to cadasil. The site maintain a list of doctors who have some experience with the disease. But I always felt that anyone who has experience with vascular dementia, already knows as much as anybody can expect and since there are no treatments for disease, all you can do is get someone to treat the symptoms anyway, and the symptoms are common neurological symptoms...so why go looking for someone who knows the disease. It is a genetic disease, and neurologists don't get much, in any, genetic education.

Hi Amy...here is a link to a cadisal site...http://www.igive.com/welcome/warmwel...fm?c=32891&m=0

Amy,

Hello and welcome to NeuroTalk. Great to see you have come to be with us. You will find a great number of caring, supporting members here willing to help each other as they can.

I see Alffe has given you our link to cadisal.

Again welcome, looking forward to seeing you around.

Darlene:hug:

Cadisal
 

Hello, I was just wondering how old you are. With a 37 year old and a 30 year old sons I am worried wath the future holds for them. The youngest has provin positive to Cadisal but you mentioned 'Varience" is there diferent types? Regrads Anna

Hello Amy and Welcome to our lil corner of the world. I see you've been given some good directions already, so just want to add that I'm glad you found us..

:welcome_sign:

Is that DaisyMay that I know??? :confused:

Amy, I am so sorry to hear about your MS confusion. This is something new to me..Cadisal...as a MS person, I will look this up. Thanks everyone for the info.

And Welcome Amy! I'm new here too!

Cadisal
 

It looks like we are both stunned by all this. So far all i can sea is gloom. I hope there is something happening with reasearch. With 4 children so far 2 are positive and the others are scared. They are better then me on the computer and their results have been -the more you know the more you dont want to know. Best of luck. regards Anna.

Hiya,
Welcome to Neurotalk, if you need anything just ask
Thanks

Hi, Amy! :Wave-Hello: Welcome to NeuroTalk!

I'm not familiar with Cadisal, so I would recommend that you use our nifty search engine located in the toolbar above. I hope you'll find some answers soon. :)