New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

Regular Member

Date Joined Aug 2008
Total Posts : 42
   Posted 8/7/2008 10:04 AM (GMT -7)   
I have not been diagnosed as of yet, however, know that I've had Epstein Barr in the past.  Does anyone know if there are links between EBV and fibro?  I think I read recently that there was a link between MS and EBV.
I've been to neuro for 3 years and not dx'd with MS.   I honestly feel that it's fibro.  Have felt pretty good for last 5 months and then a few days ago - WHAM!  can't think, too tired to do anything, burning in muscles - electric shock feelings - I sleep but wake up feeling like I was up all night.  redface
I never brought up Fibro to my dr - he never offered any info on it either.
dazed and confused

Veteran Member

Date Joined Aug 2007
Total Posts : 6067
   Posted 8/7/2008 11:04 AM (GMT -7)   
Hi booboos, cute name, and welcome to our family. If they have ruled out MS, lupus and RA it could very well be fibro. Please read the fibro 101 thread, second thread on first page. There is a great deal of info in it and a list of symptoms. Some are surprised at how many symptoms fit them.
We have some with EBV that I'm sure will give you some input on it.
This is a great forum and you will learn a lot on here.
luv and hugs
Forum Moderator Fibromyalgia
Fibro,Sjogrens, Anxiety, Gastroparesis, IBS, Gastritis, Allergies, High Blood Pressure, Low Blood Sodium and Osteoarthritis
Amitriptyline, Celexa, Xanax, Synthroid, Zyrtec, Micardis, Spironalactone, Tylenol, Reglan, Lidoderm Patches and Tramadol
Co Q 10, Super B Complex, Extra B12, Multi vitamin

Regular Member

Date Joined Jun 2008
Total Posts : 168
   Posted 8/7/2008 11:09 AM (GMT -7)   
Hi booboos and welcome to the family! In June this year, I was dx'd with fibro, cfs and cebv......the "c" in cebv means chronic/reoccurring. My first 2 rheumatologist visits, 7 weeks apart, were designed to get the first specific blood test results to rule out other diseases before giving a dx of fibro or cfs and start me on a newer treatment regimen of glutathione/atp injections once diagnosed (designed to relieve fibro/cfs/cebv symptoms by boosting the immune system & fighting off free radicals). The second visit was to compare the second test results with the first and to discuss how I felt.....any improvements or degradations.....and continue with another six weeks of injections leading up to a third visit for more comparisons and evaluations. From what I've learned from my rheumy and been able to gleen off of numerous internet sites, there does appear to be some kind of link between cebv (the chronic form) and fibro & cfs. My first blood test showed the ebv count to be through the roof......the second one showed it as only slightly high but my gabba globulin count as being low (another link to immune system function).

What does this means that I've felt the best I have in years over the last month and a half with only 1 minor flare of fibro/cfs appearing during that whole time and little or no ebv symptoms. The vast majority of people in this country have been exposed to Epstein-Barr with many developing mononucleosis or mono symptoms while others never do. Once exposed though, it will show up in a specific blood test for exposure. There is another specific test for activity which mine shows as being chronically active, thus the dx and treatment. A rheumatologist, especially one with real knowledge and experience with fibro and cfs, is usually more qualified to give these kinds of diagnoses through the running of much more specialized tests. I sincerely hope this helps you some.

Gentlest of hugs,
John (53)
Dx'd June 2008 with Fibromyalgia & CFS  possibly caused by chronic Epstein-Barr virus (many years of ongoing symptoms.....recently worsening)......also, previously dx'd sleep apnea, high blood pressure, hypothyroid, low testosterone, high cholesterol, heart arrythmia & headaches (all types)
Several meds too numerous to list or remember!

Regular Member

Date Joined Aug 2008
Total Posts : 42
   Posted 8/7/2008 11:21 AM (GMT -7)   

Thanks so much for the info.  I've been battling the unknown off and on for quite some time. The 3 years with the neuro was exhausting and I never did get an answer. I was supposed to go back for another MRI of cervical spine, but never went.  I have been feeling good for about 3-4 months and then it just hit me again. The foggy feeling/pain/my jaw is tight and hurts - weird pains in my head and shock feelings in my side and arm.  I have never gone to a rheumy and think I will make an appt.  I know my family dr thinks I'm a hypochondriac and I've tried to stay away from the office. He said that I'm "hyper-sensitive" - huh??? tongue

Thanks again for the info and input Im not sure about the EBV being chronic - he never said - I also had former human parvo virus in the blood too. Neither was active at the time of the test.  I get migraines, tension headaches, back pain neck pain, muscle aches and stiffness/burning feeling. RLS, gerd, IBS, fatty liver, bulging discs.  I had gotten a very bad infection when I gave birth to my daughter 9 years ago - Strep B - which settled in my hip joint and ate away the cartilage. Eventually, I had to get a hip replacement (4 years ago), but sometimes I wonder if that experience triggered something.


Veteran Member

Date Joined Jun 2008
Total Posts : 726
   Posted 8/7/2008 2:08 PM (GMT -7)   
booboos (LOVE the name),
There could be 2 reasons your doc called you hypersensitive.  He could have meant that you are "extra sensitive" to just the mere touch of someone grazing your arm (I have a definite hypersensitivity where I broke my leg last year-you can't even touch that area).  Or, he could have been a jack*** and meant that you are highly emotional and react to anything and everything in a bad way.  Obviously, I don't know your doctor, but since you do, maybe you can figure out what he meant. eyes
Anyway, welcome to the family.  Fibro or not, we are here for you, OK? :-)
FINALLY dxd on 06/13/08
Vicodin, Neurontin, Ibuprofen for pain-which doesn't help, BTW
Zoloft & methadone (NOT for pain) for sanity-which doesn't help, BTW
Klonopin for anxiety (Guess what?  Doesn't help!)
"I'll take the Chivas instead"
-Kelly Clarkson

Veteran Member

Date Joined Jan 2005
Total Posts : 9090
   Posted 8/7/2008 2:15 PM (GMT -7)   
Hi booboos and welcome! Just my opinion here...but so far medical science hasn't figured out what actually causes fibro nor exactly what is going on so...seems for someone to suggest that EBV causes it is a bit presumptive. Read good medical research, all that you can get your hands on. Learn all you can here and from good university or NIH studies. I use my local library all the time so try to find good books there too. Do be wary of those with the word 'Cure' in their title. When there's a cure you can bet we'll be some of the first to know.

Co-Mod Fibromyalgia & Chronic Pain Forums
Fibromyalgia, Ulcerative Colitis, Insulin dependent diabetic, collapsed disk, dermatitis herpetiformus, osteo arthritis in spine and other locations.

The only difference between genius and stupidity is that genius has it's limits. Albert Einstein: (1879-1955)

Forum Moderator

Date Joined Apr 2005
Total Posts : 17499
   Posted 8/7/2008 2:16 PM (GMT -7)   
Hi, Booboo, and welcome!  I'm glad that you joined us.  Some think that Epstein Barr can cause fibromyalgia but others think it's neurological or caused by a different virus.  The fact one knows the cause of fibromyalgia.  Everyone is guessing right now but I think they are working on finding the cause so they can work on finding help for us and possibly a cure.  Wouldn't that be wonderful! 
Again, welcome!  I do hope to hear more from you soon.
Forum Moderator/ Fibromyalgia
Fibromyalgia, Crohn's Disease, Ostomy, Diabetes, Autoimmune Inner Ear Disease, Osteoporosis
God does not give us a spirit of fear, but of power and of love and of a sound mind.    2 Timothy 1:7

Regular Member

Date Joined Aug 2008
Total Posts : 42
   Posted 8/7/2008 4:58 PM (GMT -7)   
Thanks for all the support and information!  I'm so glad that I found you guys! :-)
I do take hydrocodone for back/neck pain, klonopin for RLS, prevacid (when I remember), flaxseed oil, coq10 and l-carnitine. Probably some other stuff that I can't remember right now!!
I recently stopped taking the pain meds because I have a fatty liver and was afraid I would do more harm - but it's hard. The fatigue and general feeling of malaise is too much sometimes. The pain meds also gave me energy but  I could not take them at night because of sleep.  I also noticed for the past several years that I do have tender points inside my elbows and knees and at a point around shoulder blade.   I decided that I was going to start looking for a rheumy in my area and start from there.
You guys are wonderful and I really appreciate the information, tips and support!
New Topic Post Reply Printable Version
Forum Information
Currently it is Tuesday, November 21, 2017 4:24 PM (GMT -7)
There are a total of 2,896,459 posts in 317,904 threads.
View Active Threads

Who's Online
This forum has 157488 registered members. Please welcome our newest member, Marcos Elrod.
417 Guest(s), 9 Registered Member(s) are currently online.  Details
countingstarsx, mattamx, Doggiedo, SomeonesMom, Michael_T, Hoagie, dbwilco, garyi, cnrage

About Us | Advertise | Donate
Newsletter | Privacy Policy & Disclaimer
Follow on Facebook Follow on Twitter Follow on Pinterest
©1996-2017 LLC  All Rights Reserved.