View Single Post
Old 06-23-2010, 04:45 PM
NM_Dewey NM_Dewey is offline
Junior Member
 
Join Date: Nov 2009
Location: Belen, NM
Posts: 39
10 yr Member
NM_Dewey NM_Dewey is offline
Junior Member
 
Join Date: Nov 2009
Location: Belen, NM
Posts: 39
10 yr Member
Default

Craig,

I went through with the genetic testing mainly for my family. My grandmother (85 y/o) has terrible balance issues and slurred speech, my mother(64 y/o) has balance issues but no symptoms, older brother (41 y/o) has had an MRI that shows the cerebellum atrophy with balance issues. I am lucky to get the painful neuropathy, balance issues, speech issues...yadda, yadda, yadda. I'm 40 and thinking back have been experiencing symptoms for much longer than I thought. I've been experiencing hand/leg tremors since I was young.

Unfortunately by getting a specific dx I now have to deal with insurance and all those other things. My long term disability insurance has a "pre-existing" existing clause. Since I've only been in my current job for 10 Months and have had dr visits and testing prior to starting the job the say I have a 'pre-existing" condition, though, we had no dx. Very frustrating. I've read cases where people have fought the insurance companies on these clauses and won...but at what cost?

Thanks for your reply. Good to know others are out there...at times it gets very lonely feeling as if you are the only one facing this terrible disease.

Dewey

Quote:
Originally Posted by NeuroNixed Craig View Post
Hi NM_Dewey,

I read your original post and thought I had written it. I give you credit for going the genetic testing route. From day one when suggested by my neuro at that time, I refused on principle. I do not trust medicine, insurance, or government with information that may have a detrimental effect on my children and grandchildren, i.e. "pre-existing condition." Not to mention I would have to pay almost $7,000 and it's not covered by my insurance.

I was training for a marathon in Hawaii when symptoms hit. Within 2 years I was dependent on forearm crutches to ambulate. Misdiagnosed twice with two different types of MS, strongly suspected Hereditary Spastic Paraplegia but without a genetic marker test they would not confirm it.

Now, after 10 years for severe and progressive symptoms, the diagnosis is Spinocerebellar Ataxia and Atrophy, Cerebellar Degenerative Disease with Ataxia. Oh! And let us not forget the unrelated near fatal brain stem stroke of December 2008. Docs and neuros went nuts trying to figure out if my symptoms were stroke or disease related. Almost controlled chaos in the ER, according to my wife.

I understand, appreciate, and totally empathize with your situation. Until I find the blue ink stamp on the bottom of my foot with an expiration date, who the h*ll cares what the neuros say. Stephen Hawking has Lou Gehrig's Disease and wasn't suppose to live past high school. What's that tell you?

As our unit motto says from special ops, "Evaluate, Adapt, and Overcome!" If anybody gives you a problem, tell them they are free to go get counseling.

You are NOT alone. Thank you for sharing your circumstances.
__________________
"An American Military member, whether active duty, retired, national guard or reserve, is someone who, at one point in his life, wrote a blank check made payable to " The United States of America", for an amount of "up to and including my life.""
NM_Dewey is offline   Reply With QuoteReply With Quote