Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 11-12-2016, 05:31 PM #2
Littlepaw's Avatar
Littlepaw Littlepaw is offline
Senior Member
 
Join Date: Nov 2014
Posts: 1,537
10 yr Member
Littlepaw Littlepaw is offline
Senior Member
Littlepaw's Avatar
 
Join Date: Nov 2014
Posts: 1,537
10 yr Member
Heart

Hi Sophie and Welcome,

I am so sorry for what you're going through. We all know how frightening this can be. But you are not alone and there are definitely reasons for hope. The majority of people with CRPS (80% according to Cleveland Clinic's Dr. Michael Stanton Hicks) improve over time.

Treatment for either CRPS 1 or 2 will be very similar; pain control, exercise, PT, anti-oxidents, stress reduction etc. Though a nerve injury can have its own set of issues and be a complicating factor there is still potential for healing. I had a severe, complicated nerve injury (worst kind possible) and had to have a repair so we know that I have CRPS 2. That said my symptoms are improved and under control with ongoing treatment. Recovery was slow and took a lot of aqua therapy and gradual weightbearing but I am able to walk and do what I need each day.

My best advice is to be cautious about any nerve destroying interventions in your foot. Phenol injections for Morton's neuroma can make things worse. Surgery, if ever pursued would be best done by someone with peripheral nerve training so they know how to handle the nerve properly to prevent a true neuroma from forming. Could you have damage to the nerve from your injections? It is possible but risks for this are lower if your injections were ultrasound guided. That interdigital nerve is small as your podiatrist said but even CRPS 1 appears to have damage to the small fibers in the skin of some CRPS patients according to Dr. Louise Oaklander. I would try not to worry too much about that at this point. If it makes you feel better you could ask for an ultrasound of that nerve which would show swelling or constriction. If your podiatrist hasn't done much of that a Physical Medicine doctor who treats Morton's could take a look. The pain in your other foot could be mirror pain, something I had originally that was not true CRPS but pain jumping across the spinal cord from pain being very intense. Mine resolved as I got better.

Nerves can be really fussy. If you are having even minor swelling in your feet now that could be contributing to aggravation of the nerve which can accumulate fluid and swelling itself. Any recommendation they have for footwear may be helpful and will be conservative treatment for the neuroma. Offloading pressure and also providing adequate support to give a little space between the toes are good strategies. Make sure you have an adequately large toe box. Try toe spreaders for short periods when off your feet. Get in a pool and swim. It will help your circulation and swelling while starting imperative exercise. You might also try a round of oral steroids which are recommended as an early treatment and can break the inflammatory cycle that gets CRPS going.

Hang in there and try not to stress too hard. I know it's easier said than done. But you beat this beast once before and we're all hoping you're going to beat again!

Sending hugs and healing love,
__________________
Littlepaw

Shine Your Bright Light
Littlepaw is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Shay08 (11-13-2016), Sophie0513 (11-12-2016)
 

Tags
crps, feet, foot, podiatrist, started

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
your input please jeanb Parkinson's Disease 8 09-27-2011 08:28 PM
I really need your input!! MelodyL Alcoholism, Addiction and Recovery 15 07-22-2009 09:54 PM
Still Need Your Input, Please Virginia Therese Parkinson's Disease 11 01-30-2008 07:47 PM
Please...I need your input Virginia Therese Parkinson's Disease 5 01-28-2008 03:27 PM
Tell it like it is - Need your input! pegleg Parkinson's Disease 35 04-29-2007 08:15 AM


All times are GMT -5. The time now is 08:03 AM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.