~Chronic Fatigue Syndrome and Fibromyalgia~A place for Chronic Fatigue Syndrome (CFS) and Fibromyalgia (FM) discussion.
Welcome To EDS-Kids
EDS Kids is a support group and community dedicated to helping children and young adult who suffer from chronic pain resulting from illnesses and genetic conditions like Ehlers Danlos Syndrome and Fibromyalgia. Ehlers-Danlos Syndrome (EDS for short) is a genetic connective tissue disorder which primarily causes chronic joint pain and joint dislocations. EDS Kids is a community dedicated to helping not only sufferers of EDS but their family and friends too.
Hey guys. My fibromyalgia and CFS have really been killing me this week. My lymph nodes are the size of golf balls... and I can barely make it across the room without running out of breath. To add onto it, I'm starting to dislocate my "good" shoulder (as if there's such a thing in EDS...)
Does anyone here know of ANY type of relief for those things, especially for the constantly swollen lymph nodes? I'm desperate. My lmphs have been swollen for 4 years now! Could I have some kind of tiny viral or bacterial infection sitting around in my body because I'm slightly immune deficient, causing my lymphs to be swollen?
Ugh... I'm running around in circles! Someone! Anyone! Any ideas...?
-Johnna
__________________ I'm an admin so please let me know if you need anything! =]
Johnna - 22- EDS III, FMS, CFS, Hashimoto's Thyroiditis, HPA Axis Dysfunction, POTS, Meniere's Disease, Clinical Depression. CURED of Adrenal Insufficiency! =] I'm a ninja, zomg!
Oh Johnna! I'm so sorry to hear that you're feeling so poorly too....my CFS has been flaring for almost a month so I feel your pain.
Sadly I don't think there is anything you can do regarding the fibro. Just rest as much as you can I would say. Regarding the lymph nodes, I'm sure you've discussed them with a doctor, right? If you haven't, you know where to start lol!
(((hugs)))
__________________ Gwendolyn
*21 years old*
EDS (Hypermobility and Classical), POTS, NCS, CFS, IBS, GERD, Fibromyalgia, a sliding hiatal hernia, Depression, Gastroparisis
I am beginning to learn that it is the sweet, simple things of life which are the real ones after all.
~Laura Ingalls Wilder
The best and most beautiful things in the world cannot be seen or even touched. They must be felt within the heart.
~Helen Keller
I would go to a your doctor about the lymph nodes, it sounds to me like you could have some kind of infection or something. For the fibro what i do is rest a lot and use a heating pad a lot so that I can get my muscles to relax and loosen up a bit.
I hope you feel better soon.
__________________ Staci Jo *21*
When the world says "Give Up"; Hope whispers "Try one More TIme."
Classical EDS, Fibromyalgia, Depression, Anxiety, DDD & Bulging disk at L4-L5
I'm a moderator here and if you wanna chat or have any questions I'm here.
(I remember you being on a muscle relaxer...that helps a lot of people too)
As for the CFS...I have swollen lymphs from time to time...most of my docs aren't "into" CFS and Fibro so the thought is that I could have a chronic infection that just flares up...I'm supposed to see an Infectious Disease doc but I never went. Did your doc say the swelling is from the CFS???
__________________
What I always wish I was doing ---> :
I'm one of the mods here...feel free to PM me anytime (or IM too)
My doctor contributed the swelling to the Fibro... but has also told me I should see an infectious disease specialist. The only problem with this is that my dad just got let go of work yesterday, so we're still not quite sure if I still have that medical insurance. I guess we'll have to wait and see. ._.
-Johnna
__________________ I'm an admin so please let me know if you need anything! =]
Johnna - 22- EDS III, FMS, CFS, Hashimoto's Thyroiditis, HPA Axis Dysfunction, POTS, Meniere's Disease, Clinical Depression. CURED of Adrenal Insufficiency! =] I'm a ninja, zomg!
I am so sorry to hear that all of you are so young and are suffering with this horrible disease. My aunt has been struggling with fibromyalgia for many years and swears by the healing benefits of epsom salt. She has been soaking for 20 minutes a day and buying the same box for years. However, we were in Walgreens a couple days ago and we found a new epsom salt product in the first aid aisle called Pepsom sports. She decided to try it and really liked the spearmint scent and they way she felt after soaking. Just thought I would pass along this information to anyone struggling with this disease. Hope you all feel better!