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)


advertisement
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 08-01-2012, 04:21 PM #1
AliM AliM is offline
Junior Member
 
Join Date: Jul 2012
Posts: 21
10 yr Member
AliM AliM is offline
Junior Member
 
Join Date: Jul 2012
Posts: 21
10 yr Member
Default Difficulty walking: CRPS foot

I'm just hoping there's somebody else who has gone (or is going) through a similar situation and can help me out.

I woke up in December with this in my left foot, and it took until July before I finally found a doc who was able to nail down my CRPS diagnosis. Because it progressed so many months without a diagnosis or focused treatment, it has gotten bad pretty quickly. My new doc put me on Gabapentin, which has been a miracle drug for me. Now sheets and blankets and socks against my foot don't bother me any more, we can rub my foot without problem except for the sesamoid area which is incredibly tender still. (X-rays show a darker spot there--maybe what started this.)

Trying to avoid that sesamoid area has created somewhat of a club foot. And the swelling is CRAZY. Various docs prescribed all sorts of meds since December to try to control the swelling, but not a single thing worked. It's so bad I can't even get a shoe on. I wear an orthopedic walking boot every time I leave the house, which helps take the pressure off the painful ball of my foot and it...well, gives me a shoe to wear. Regardless of what I do or how much I'm on my feet, by 4:00ish my foot and ankle become the size of Texas.

Between the swelling and the tender ball of my foot, walking is excruciating. I dread having to walk across the house, even. Every single step is excruciating. Luckily I'm a former competitive tennis player, so I learned years ago to play through pain, so that's helping me cope. But at the same time, remembering how active I used to be is SO discouraging when I can't even walk 2 steps without pain. Going for a walk with my family is impossible. Half hour of grocery shopping is my limit before the pain and exhaustion makes me snippy and grumpy. (And I certainly don't want to be snapping at my kids or hubby!)

So...what's my future? Will this get better with time? Would physical therapy help? (I'm skeptical about PT with the swelling and sesamoid "injury.") Is there anything I can try that will ever allow me to get back to a somewhat normal existence? (I sure miss tennis, but would be happy to slowly amble someday without pain...)

Has anyone else dealt with this? I know everybody's CRPS is so very different, but I'm hoping for hope...
AliM is offline   Reply With QuoteReply With Quote
 


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
Hi, first posting,new member, CRPS in foot lucky853 Reflex Sympathetic Dystrophy (RSD and CRPS) 21 10-02-2013 12:29 PM
Foot turning in when walking BARBARA356 Myasthenia Gravis 1 07-22-2010 03:11 PM
problem with walking and foot pain Jim091866 Parkinson's Disease 1 06-15-2010 12:20 PM
New I have CRPS IN RIGHT FOOT. Azaila Reflex Sympathetic Dystrophy (RSD and CRPS) 6 02-10-2010 04:18 PM
difficulty walking and tailor's bunion Jim091866 Parkinson's Disease 3 09-30-2009 05:31 PM


All times are GMT -5. The time now is 11:28 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 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.