FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
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) |
Reply |
|
Thread Tools | Display Modes |
|
![]() |
#1 | ||
|
|||
Senior Member
|
If I hear one more person or doctor tell me oh you would feel better if you just exercised more and lost weight, I think I will SCREAM!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!
![]() Last edited by RSD ME; 11-07-2013 at 08:19 AM. |
||
![]() |
![]() |
"Thanks for this!" says: | pooh_ac (11-07-2013) |
![]() |
#2 | ||
|
|||
Senior Member
|
Ahhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh hhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh hhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
|
||
![]() |
![]() |
"Thanks for this!" says: | pooh_ac (11-07-2013) |
![]() |
#3 | ||
|
|||
Senior Member
|
RSD and people who don't understand RSD SUCK!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!
OH YEAH, And my life SUCKS because RSD and people who don't understand RSD SUCK!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! |
||
![]() |
![]() |
![]() |
#4 | |||
|
||||
Member
|
![]() Sorry you are feeling bad! I was actually going to post about weight gain and exercise tonight. I am lucky my doctors don't say things like that to me.
__________________
Zookeeper ~Shelly~ |
|||
![]() |
![]() |
"Thanks for this!" says: | RSD ME (11-07-2013), St George 2013 (11-07-2013) |
![]() |
#5 | ||
|
|||
Senior Member
|
Much like the the dreaded "it's all in your head" line, I think all (or at least most) of us who were at all overweight before or became sedentary after the development of our pain issues have heard some variation of the "you would feel so much better if you just got more exercise" line.
Have you been tempted to stress your body out even more by pushing your body even harder so you could lose weight JUST so that you could tell that doc to stuff it ? BTDT ! If it would make you feel any better, tell that doc a story about your online pal who DID exercise more, who DID lose a lot of weight.......and who STILL has the same severe RSD pain. Better yet, have the schmuck doc call me for a little "chat" and I'll tell him all about the PROOF that his little plan (which we all know is just to cover for the fact that he doesn't have an actual reasonable treatment plan for you) DOES NOT WORK. You might also remind said dear doctor that your difficulty with proceeding with his plan is that your severe pain is what is preventing you from exercising more. Challenge HIM. If he wants you to exercise for an hour a day, tell him that you'll be HAPPY to, just as soon as he brings your pain level down to a 0 or 1/10 for 24 hours so that you can sleep and feel comfortable enough to get out there. Make the commitment, promise him for each day he eliminates your pain that you vow to get out there and exercise. I'll bet that'll shut him up ![]() I spent years hoping that I could magically lose weight and exercise more, so that I could tell the physiatrist that WC sent me too where he could "stick" his opinions and advice. In the years since, I found a doc who has a clue and has tried to help me manage my pain, although WC denials have limited what treatments that we can do. At least he addressed my pain management needs and helped me get to a place where I felt I had SOME control. Last year, my mother was dx'd with Parkinson's and dementia after a fall and lengthy rehab. Years ago, she used to joke that she didn't need long term care insurance; she said she had "paid" for something better......a nursing degree for her eldest daughter (me), so she should get all the care she needed. That wasn't a bad plan....until I got broken ![]() The same month my mother was hospitalized, I had several important doctor appointments. I talked to each of them about my concerns for my mom.....and my need to get MORE control over my pain issues and increase my activity tolerance. My ortho who gave me steroid injections for my bilat. hip bursitis (related to my fibro). My shrink changed my antidepressant. My neuro MARKEDLY increased my narcotics. My rheumy eventually put me back on an anti-inflammatory and has helped to address my energy levels. All of them worked to get me to the point where I could get out and start moving. Walking has been my thing. I've tried to "upgrade" that to running, but that caused worsening RSD neck/arm pain and caused significant issues with my "itises" from fibro: I couldn't run and limped with walking from new plantar fasciitis and had worsening bilat hip bursitis and bilat knee tendonitis. Any kind of bouncing or dancing type cardio also seems to worsen the "itises" and is HORRENDOUS on my neck/arm RSD pain. I can now do some stretching, but haven't done well with attempts at weight lifting. Walking is my thing. Over a year and a hundred pounds lost later, I can tell you that I do indeed feel better..... IF I take a lot of narcotics. If I don't take the meds, the RSD pain is there, worse than ever. Tell your doc that I'm waiting for my pain to magically get better because of exercise.
__________________
. Gee, this looks like a great place to sit and have a picnic with my yummy bone ! |
||
![]() |
![]() |
"Thanks for this!" says: | Brambledog (11-07-2013), Hopeless (01-11-2014), Nanc (11-07-2013), RSD ME (11-07-2013), St George 2013 (11-07-2013) |
![]() |
#6 | |||
|
||||
Member
|
Quote:
Indeed I have, and it was an EPIC fail! This was a fantastic post and man oh man can I identify. And Renee, I'm so sorry. Hang in there girl. What was said to you by this doc was completely ignorant.
__________________
CRPS II Full Body via L5-S1 Discectomy Surgery in 2004 Symptoms started upon waking from surgery in right foot/leg, mirrored to left foot/leg and then EVERYWHERE else. Vision without action is a daydream. Action without vision is a nightmare. Japanese proverb, |
|||
![]() |
![]() |
"Thanks for this!" says: |
![]() |
#7 | ||
|
|||
Senior Member
|
I think finz hit the nail very firmly on the head here. Couldn't agree more, and very elegantly put
![]() Renee, I'm sorry you have your burden added to by such poorly-thought-out ignorance and lack of compassion. Sounds like you could maybe think about trying a new doc, or you could express to him how you feel about what he says. I used to suffer dreadfully from White-coat Syndrome, and just agreed with everything they said (still can if I'm feeling very low ![]() I hope things feel easier soon for you. Try a bit of pampering chick - some nice music, nice smells, self-massage (very soothing) and something altogether pleasant to eat and drink ![]() ![]() Hark at me. Lol. Take care of yourselves and keep being who you are, whatever size that might be ![]() Bram.
__________________
CRPS started in left knee after op in Aug. 2011 Spread to entire left leg and foot, left arm, right foot. Coeliac since 2007. Patella femoral arthritis both knees. Keep smiling! . |
||
![]() |
![]() |
"Thanks for this!" says: |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
Ugh I wanna scream | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
SCREAM!!! just a vent | Chronic Pain | |||
Ugh I could scream | Bipolar Disorder | |||
I just want to SCREAM.... | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Do I scream, or do I cry?? | Sanctuary for Spiritual Support |