LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » My (shortish) story, and would like input

 - UBBFriend: Email this page to someone!    
Author Topic: My (shortish) story, and would like input
6Hypnone
LymeNet Contributor
Member # 47629

Icon 1 posted      Profile for 6Hypnone   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I supposedly have fibromyalgia. Dx'ed in late 2014 when my mom was very sick. She died dec 2014. It has been said that my symptoms arose from her dying and my poor sleep and that if those are fixed, this would end.
I've had the typical lyme test (neg) and an ISPOT test (which I was told was as good as Ingenex) and that was neg, but my IFN-Y secretion unstimulated was high, and it indicated either a food sensitivity or a co infection, as it said that meant my immune system is active.

I've had DNA testing and metabolic testing. Am having neurotransmitter testing tomorrow. I am heterogyzous for MTHFR as well.

My symptoms in the beginning were (and still are at times) what felt/feels like bone pain..achy and growing-pain feelings, mostly in joints but now always.

Now I halso have a little tingling in one hand, and my left foot (which has a bone spur, and is confirmed that a nerve is somewhat crowded and inflamed there), as well as shocky sensations, nerve pain (sometimes sharp and sudden--painful).
The latter symptoms (the shocks, not the nerve pain) I first noticed on Gabapentin, so I went off and they eventually went away. Went back on same happened, came off. Tried Lyrica too. Both at low doses.

Now I am weaning off Gaba another time to see if it helps, so far, no.

I've also had a 'tickle' sensation in my nerves...hands, head, feet...it's maddening...I felt suicidal.

Anyway, has anyone heard/had the Ispot test? Do you have these symptoms? If so, was it lyme? And if NOT, what was it?

Feel very free to PM me as well.
I have some docs in mind, thanks to a friend outside of this and from here. I am in IL, sw suburbs of chicago.

Posts: 606 | From sw suburbs of chicago, Illinois | Registered: Mar 2016  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can you tell us more about your Lyme testing? Did you have the Western Blot, and if so, what were the results?

Are you taking something for your MTHFR? Your symptoms sound nervous system-related and B vitamins are closely associated with that. Plus, when you don't methylate, you don't get rid of toxins. Perhaps toxins and heavy metals are part of the issue. I would see an alternative doctor who understands MTHFR.

I had an "Array 10" for food sensitivities. It was great. I found out all kinds of foods I was reacting to. That helped. When my gut is healed, we think I'll be able to add most of them back in, but it was good to know what was causing some random reactions.

So, I'd look at 1) MTHFR treatment 2) What are the food sensitivities? 3) Heavy metals .... with an alternative practitioner. Once you get all this stuff (and the other stuff they find) treated, if you have symptoms, then worry about whether the remaining is bacterial or viral, if you even have remaining symptoms.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you have Lyme, stress can bring it on more strongly, since stress weakens the immune system.

I was first diagnosed with fibromyalgia before finding out I had Lyme, as are so many.

Bone pain and nerve symptoms sound suspicious for Lyme.

IGeneX can send you a free testkit. If you qualify as low-income, www.lymetap.com covers 75% of testing costs.

Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Check your GABA supplement. Does it contain Vit B6? It could be adversely affecting your nerves.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have you ever taken a fluoroquinolone antibiotic (cipro, levaquin, avelox, etc...)?

They can cause the persistent problems you described long after taking it.

Posts: 2839 | From California | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.