Physical Therapy for Complex Regional Pain Syndrome with Michael Wiechec, PT, MCMT | RSDSA
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- Опубліковано 30 лип 2024
- To learn more about complex regional pain syndrome (CRPS) and reflex sympathetic dystrophy (RSD), visit Reflex Sympathetic Dystrophy Syndrome Association (RSDSA)’s website at rsds.org.
View the presentations from Treating The Whole Person: Houston, and our previous conferences, at rsds.org/educational-presenta...
#RSDSA #CRPS #RSD
Great info
To Mr. Weichec:
I was wondering if we could talk about care, I live a few hours away from Houston and just noticed the area these were taking place. I'm also one of those who has just been let slip bc no one will listen and worse. I developed CRPS, possibly after my injury, possibly after the surgery. Idk and there's a lot Idk bc of the "treatment" I've received. And here I am 2yrs later, can't walk, muscle atrophy, and a collapsing arch now too. I'm all kinds of messed up from this and lack multiple levels of care, even basic. There's so much that's taken place and I'm... I'll say exhausted bc I know you gotta know what I really mean. And I have no help, I have no care or direction. I'm trying to do everything alone with what information I can pick up. Considering it immediately gets argued when I bring up info from here...Idk what to think anymore and I need help. The first few minutes of this video explained way more than I've gotten so far. I'm really hoping you can help me somehow.
Edit: Grammar
Very Nice Mr Wiechec,
I am wondering if you know where Todd Merry might be?
I'll forward you question to him
I have been through all kinds of physical therapy and at first it was helping but then I got hurt from just working more hours 25 instead of 18 and walking more and then I started getting the symptoms back and ever since then physical therapy has just made it worse and I notice it the next day. It last for weeks and months unless I start moving then it starts slowly starting to calm down I might be misdiagnosed but they can’t find what’s wrong with me and I have a purple foot unless I lay on a bed.
I’m 6 months in and can’t walk only sort of relief is laying in bed with my foot elevated. I noticed u posted this a year ago seeing if u are now walking?
@@Skippystan I have days were I have more strength but I have to use crutches to move some of the time I can use 1 crutch. I can sit in a chair for about a half hour before I start getting weak and my left leg starts turning a darker shade. My muscles especially in my back and hip will become weak and painful without doing anything or not that I noticed. I have to sit on my bed to get much relief. It’s like having storms and hurricanes periodically throughout the day. I have to take vitamin d if I’m off it for too long I wake up with even more back pain and can’t regulate my temperature feeling cold no matter what. I could write a novel about this stuff it’s so complex. I also loose memory when the pain starts becoming unbearable really weird.
@@brawlnoob7791 it’s definitely a nightmare that’s for sure, thr daily struggles of pain and not being able to walk is frustrating.
Is this today?
June 2019
Please don’t read every slide