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Replies to "Hi. I cannot recommend a doctor in particular for you. Frankly, in my experience there is..."
I have PTS, I was blessed to be diagnosed 2 1/2 months into it, though it is the most painful experience in my life. I live in the Chicago area and this is so uncommon i have had a hard time finding any info or even neurologists who have treated more than one person. I have the rarer nerves in my arm involved and cannot find a dr who has ever treated a woman with this. Anyway, it slowly improves, sleep when you can, positioning, heat, tens unit, exercise, all help. I still take occasional pain meds, but time heals, slow, slow, so hang in there, sleep sitting in a recliner, only way for a long while. Ive been ill with it 16 months, still have severe denervation, no strength, but i do pilates 3 days a week to keep. Strength,
Thank you for your information regarding the Thymoma. Mark has had numerous MRI's and CAT scans and nothing shows any tumors or suspicious shadows, etc.
As a result of inactivity, he has developed blood clots in his arm and is now on Eliquis (blood thinner). Do to the swelling in his arm and hand, PT is not an option at this time. But he does daily exercises to maintain some ROM in his right arm. We go for a new ultrasound end of February to check on the clots.
Also working with a pain management doctor to contain the pain. A once a month visit to renew prescriptions.
It's just SO frustrating to have no known cause, no diagnostic testing, no definite timeline for it to run its course or how complete a person's recovery may be.
I appreciate finding this Group and am sure we can learn a lot and hopefully, help someone else.