Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 04-10-2015, 08:02 PM #11
madisongrrl's Avatar
madisongrrl madisongrrl is offline
Member
 
Join Date: Jul 2014
Location: Midwest
Posts: 584
10 yr Member
madisongrrl madisongrrl is offline
Member
madisongrrl's Avatar
 
Join Date: Jul 2014
Location: Midwest
Posts: 584
10 yr Member
Default

Quote:
Originally Posted by Healthgirl View Post
$1200 Ouch!
It was a 1.5 hour consult and he went over all my paper work.
Yeah that is pricey... but I assume a large chunk of that is lab work. How much did the consult part cost? It is nice to get someone with a different perspective to take a lot of time with your case.

Could you refresh my memory? Did you take the Igenex test in the past and have a borderline result?

Quote:
Originally Posted by Healthgirl View Post
He seems to be the only doctor who is curious as to why my ferritin is so low and why my copper is deficient.
Malabsorption due to autoimmunity? Have you found any good medical literature on the ferritin and copper levels? Clearly something is going on with that whether or not it's directly related to your SFN.

Quote:
Originally Posted by Healthgirl View Post
I must admit that I went in with the attitude of "of course this guy is going to say I have lyme with all my symptoms and go on about how flawed the CDC testing is", but yet I felt it was necessary to explore this option as no one has been able to help me.
I totally agree with you and will probably be headed down this same road shortly. All avenues need to be explored.

Quote:
Originally Posted by Healthgirl View Post
Lyme doc said plaquenil in conjunction with antibiotics can fight Bartonella...........I just hate medicine, but I don't know what I have to loose. I want my life back. I'm so freaking confused and have much to absorb as this was just last night that I got back from the appointment.
What do y'all think?
I think it's also difficult sorting out if your Sjogrens disease caused SFN or if it is happening in addition to it. I hate taking any kind of medicine too, but if I were in your shoes I'd give it a shot. At least for a little while to see if you can smack down some of this potential autoimmunity and/or infection.
madisongrrl is offline   Reply With QuoteReply With Quote
 


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
MG and LYME michaelunty Myasthenia Gravis 5 04-22-2015 06:24 PM
lyme and ms... novo20 New Member Introductions 1 09-04-2013 12:28 AM
ALS/Lyme jccgf ALS 7 08-20-2011 03:43 PM
I have just been Dx'd with Lyme Quahog Lyme Disease, Shingles and Other Microbial Conditions 12 11-06-2009 05:34 PM
Lyme LizaJane Peripheral Neuropathy 2 12-18-2008 07:15 PM


All times are GMT -5. The time now is 10:39 AM.


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.