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FMS ForumsGeneral & SupportSevere Elbow Pain
04/21/2012 11:15 AM
SweetJulie62
SweetJulie62
 
Posts: 26
Member

Not likely i go to comm service clinic and they are not offering me much help just ibuprofen and flexaril.
I am a Certified Medical Assistant any comments, suggestions are from personal experience and not offered as Medical advise.
Reply

04/21/2012 11:50 AM  Top
RLFORTIN
RLFORTIN
 
Posts: 27
Member

I have pain in my elbow that affects my hand, fingers and forearm. Had an EMG and I have Ulnar Nerve Damage. I get pain, muscle weakness and tingling. Have you have a EMG/nerve conduction study?

Nelle

Nelle : )

04/21/2012 01:27 PM  Top
hatbox121
hatbox121
 
Posts: 10501
Group Leader

Weakness that is progressive is more worriesome than the pain. An EMG is a good call to check for any potential nerve damage that might be there. If you don't have insurance check out the no insurance/low income thread that is stickied in the general forum.
Amy~ “When you come to the end of your rope, tie a knot and hang on.” ~Franklin D. Roosevelt

Current dxes-Ehlers Danlos Syndrome, Mitral Valve Prolapse w/regurg, 2 other heart valves with regurg, POTS, DDD, scoliosis, various OA, polyneuropathy of unknown origin, SI joint dysfunction/fusion/collapse, chronic rotar cuff tendonitis, impingement syndrome of the shoulder, chronic bursitis in various locations, degeneration of the sternum, vertigo, GERD, FM, CFS, CPS, various bone marrow lesions, brain lesions of unknown cause, migraines, TMJ, vertically bulging discs, Raynaud's, anemia, tinnitus, high copper levels, borderline glaucoma, colon polyps, intermittent RLS, Vit D deficiency, depression, Eye accomodation disorder, Essential tremor, recurrent kidney stones, sacral spine disorder, inflammed tendons, and inflammation of spinal nerves(no specific dx).

I'm am not a dr. I am not a substitute for a dr. All advice I give is based on research and my personal experiences.

04/22/2012 06:54 AM  Top
Adewyn
Adewyn
 
Posts: 4975
Group Leader

oooo mmmyyyyy gggooooddddessssss... yes.!!! the fibro points urt all the time but before i started building my muscles back up.. holy crap there were days i couldnt even open my elbow joint up... now at i am uilding muscle in that area... yes my fibro points hurt... but i have had far less "attacks of this pain.. i usualy get it when i have over used (obviously) OR Slept on my arms wrong..... hang in there... if you dont have muscle relaxer ask for one take it at night and see if it helps after a few days.... keep moving those arms and hands... and shoulders...hugs andlove

04/22/2012 04:51 PM  Top
SweetJulie62
SweetJulie62
 
Posts: 26
Member

Thanks for the advise but currently i am in pain 24/7. Difficulty walking i am going to start walking and increase daily.
I am a Certified Medical Assistant any comments, suggestions are from personal experience and not offered as Medical advise.

Previous discussions I participated in:
188/118
Another Loss
I have RSD(CRPS)

04/26/2012 06:38 PM  Top
SweetJulie62
SweetJulie62
 
Posts: 26
Member

Marilyn,

Nice to hear from you. All my rheumatoid tests came back as normal so i will have to live with the back pain. My tennis elbow has gotten so painful i can no longer lift a gallon of milk mostly from the severe pain. Anytime i do any house hold chores it hurts for the next few days, throbbing, very swollen i am afraid it will get so bad i will not be able use my elbows.

I talk to a lawyer about disability, i have to get him some info. I have no family, nearby and the same for friends. But i am pushing on.

Enough about me, how are you

I am a Certified Medical Assistant any comments, suggestions are from personal experience and not offered as Medical advise.

Previous discussions I participated in:
188/118
Another Loss
I have RSD(CRPS)

04/26/2012 07:19 PM  Top
SweetJulie62
SweetJulie62
 
Posts: 26
Member

No i have to go to a comm clinic so i am left with ibuprofen and flexaril i do not want drugs i want something done.
I am a Certified Medical Assistant any comments, suggestions are from personal experience and not offered as Medical advise.

Previous discussions I participated in:
188/118
Another Loss
I have RSD(CRPS)

04/26/2012 07:53 PM  Top
mabri
mabri
 
Posts: 4710
Group Leader

Julie,

You are not alone, we are here for you always. I know it's not the same as having family nearby, but we care for and support you.

I know you do not want drugs, but unfortunately with fibro there is really nothing they can do. We can do some things to help ourselves, but meds are so helpful in helping us lead a functional life. I hope you can get to a dr to get the attention you need. HUGS

Please do not take anything I say as medical advice. I am not a doctor.

**Becky**

04/30/2012 10:11 AM  Top
SweetJulie62
SweetJulie62
 
Posts: 26
Member

Thanks for your support! I need all of you.
I am a Certified Medical Assistant any comments, suggestions are from personal experience and not offered as Medical advise.

Previous discussions I participated in:
188/118
Another Loss
I have RSD(CRPS)
Reply

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