advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 09-16-2016, 12:08 PM #20
en bloc's Avatar
en bloc en bloc is offline
Senior Member
 
Join Date: Feb 2011
Location: Shenandoah Mountains, VA
Posts: 1,250
10 yr Member
en bloc en bloc is offline
Senior Member
en bloc's Avatar
 
Join Date: Feb 2011
Location: Shenandoah Mountains, VA
Posts: 1,250
10 yr Member
Default

The letter helps a bit, but he's not very specific about what he's referring to in regards to the neurological manifestations...as he mentioned SFN, disequilibrium, and the SVID/SVD. He doesn't mentioned CNS...and there is a difference between neuro manifestations and CNS (because SFN is a peripheral development, not CNS).

He only brings up the SVID as it does appear in those with Sjogren's...which it does. He doesn't refer to this as the main neuro symptom. He states the SFN and disequilibrium as main symptoms/problems. Therefore, I think he's addressing the immunosuppression as being related to helping these...as he would consider this treatment if both Sjogren's & neuro manifestations are confirmed (which are his two questions).

I DO think there is possibly something neuro related with the disequilibrium/vertigo. I agree that autonomic testing would be a good idea as maybe this disequilibrium/vertigo is a vagus nerve problem. Have you read anything about the vagus nerve? It can cause a variety of problems, including unusual dizziness.

I think my best summary of his letter is that he feels immunosuppression is best course IF there is confirmation (from other doctors) of both Sjogren's and neuro manifestation of Sjogren's (which he is referring to SFN and the disequilibrium/vertigo). This would be a normal course of action to treat SFN resulting from Sjogren's. I don't think they know what is causing the disequilibrium, but they likely think it's Sjogren's or neuro related. Keep in mind that autonomic dysfunction (which may be causing the vertigo) IS related to SFN...and is peripheral not CNS.

There is no indication he is considering a CNS involvement...thankfully!! That should ease your mind, for sure.

I also agree that Cellcept would be a good option to try once all your testing is done (don't want to medicate before you complete testing).

Last edited by en bloc; 09-16-2016 at 12:26 PM. Reason: Summary:
en bloc is offline   Reply With QuoteReply With Quote
 

Tags
disease, news, sjogrens, svd, symptoms


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
waiting for SFEMG test results n8swife Myasthenia Gravis 2 03-30-2011 05:15 PM
Possible MG, waiting on test results...questions shalynn Myasthenia Gravis 8 06-27-2010 02:49 PM
Waiting for MRI results Freesia38 Multiple Sclerosis 6 08-31-2009 11:25 PM
Waiting for results of Mitochondrial and CADASIL Merle Metabolic Diseases / Mitochondrial 1 12-12-2008 10:52 AM


All times are GMT -5. The time now is 07:21 AM.

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.