advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 08-25-2020, 12:54 PM #7
tkrik's Avatar
tkrik tkrik is offline
Wise Elder
 
Join Date: Jan 2008
Posts: 8,403
15 yr Member
tkrik tkrik is offline
Wise Elder
tkrik's Avatar
 
Join Date: Jan 2008
Posts: 8,403
15 yr Member
Default

I'm sorry you are having such a rough time. It's so frustrating when we feel the doctors aren't listening and don't have that validation. I think we all have been there to varying degrees.

Have you discussed any of this with your primary care doctor? They may be able to help get the ball rolling quicker and in the right and/or different direction. Unfortunately, there are a number of diseases that mimic MS. Your PCP may be able to come at it from a different angle, maybe testing for other autoimmune diseases and even going to a rheumatologist.

It's really hard to be struggling and have no definite answers to anything. Hang in there and let us know how you are doing.
tkrik is offline   Reply With QuoteReply With Quote
 

Tags
cope, feel, flare, symptoms, waves


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
Copper Deficiency - Mimics MS? Koi13 Multiple Sclerosis 17 05-14-2013 05:38 AM


All times are GMT -5. The time now is 09:39 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.