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-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Broadway Baby and all............. (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/13318-broadway-baby.html)

Barb2406 02-13-2007 12:48 AM

Broadway Baby and all.............
 
:hug: BB,

Thanks for the info about the docs in Eastern PA. I am going to have to change my signature as I found a PM Doc that believes I have RSD!!!!!!!!!!!

Finally I found a PM Doc, went to him today and he did an epidural lumbar block, he also ordered the Duragesic patch at 50 mcg's. For the first time in months I am below a 6 on the pain scale.

I do have a question for anyone that might know the answer. In the last 2 weeks I started having the burning on the instep of my right foot,this is where my RSD started. Anyone have any idea why it took almost 8 years for this awful burning to start?????

;) :hug: :eek:

BroadwayBaby 02-13-2007 12:36 PM

Barb,
I'm glad I could help, and CONGRATS on the treatments!

As for the change in symptoms - I've had RSD for 8 years now, and have very few of the same symptoms now that I had when it started - it seems that the disease just tends to change (not evolve, really) over time.

I started with burning pain in the back of my right knee - now, my symptoms change on a daily basis! Burning, tingling, aches, sharp pains, front of the knee, back of the knee, feet, left leg......sometimes all, sometimes only one or two!

I know that's not necessarily helpful, but I would say that it's definitely important to keep your doctor updated on your symptoms - if things are progressing/changing, the doc needs to be aware so that your treatment can be modified if necessary.


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