Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 02-28-2011, 09:28 AM #13
Snoopy's Avatar
Snoopy Snoopy is offline
Magnate
 
Join Date: Sep 2006
Posts: 2,280
15 yr Member
Snoopy Snoopy is offline
Magnate
Snoopy's Avatar
 
Join Date: Sep 2006
Posts: 2,280
15 yr Member
Default

Quote:
Originally Posted by daisy.girl View Post
Can I ask why you did not try a DMD? Are you still able to walk?
In 1985 there were no DMDs. Betaseron was the first DMD to become available to the general MS population in 1993...by lottery. I did have a lottery number. At the time there were alot of unknowns about Betaseron since it was the first of it's kind. As my number came up I decided to wait and see.

Through the years I have simply decided I prefer to take my chances with the disease. I, personally, do not believe these drugs work as well as we are lead to believe. The disease is still not understood and I often wonder how is it possible to effectively treat a disease under those circumstances.

I don't walk right but I do walk and unaided for the most part.

However, I do like and use trekking poles when I will be out doing a lot of walking. My balance sucks and always has, trekking poles help to compensate and helps my endurance.

My thoughts and opinions on the DMDs are just that...thoughts and opinions. Not everyone will have my experience.

To use or not use a DMD is a personal choice and neither choice is wrong. Do what you feel is best for you. The choice you make is the one you feel the most comfortable with and the path that leads to the least regrets
__________________
Dx RRMS 1984
Snoopy is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
daisy.girl (02-28-2011), dmplaura (02-28-2011), Kitty (02-28-2011)
 


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
How would you describe your facial numbness?? jiggered Multiple Sclerosis 13 12-04-2010 07:27 AM
How do you describe your RSD to others? InHisHands Reflex Sympathetic Dystrophy (RSD and CRPS) 30 05-03-2010 09:51 PM
Can someone describe the differences... dahlek Diabetes / Insulin Resistance / Metabolic Syndrome 2 01-26-2009 12:03 PM
a new way to describe what MS is to me sassy Multiple Sclerosis 13 01-21-2009 08:43 AM
Describe how you went numb? sugarboo Multiple Sclerosis 18 02-23-2008 01:15 PM


All times are GMT -5. The time now is 11:57 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.