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 | |||
|
||||
Member
|
Quote:
![]() ![]() ![]() ![]() ![]() ![]()
__________________
I Will Always Believe in Poems, Prayers And Promises Love, Desi . |
|||
![]() |
![]() |
![]() |
#2 | |||
|
||||
Magnate
|
I am so glad that you have found a Dr. that cares and that knows enough about RSD to diagnose it and run with the blocks. When you talked about how your Dr. treated you, I thought of mine. He's been right beside me for 17 years first with other problems and then the RSD. I believe knowing we have a Dr. that is willing to help us with the RSD is a first step. Someone said something about the weekends being the worst because the Dr. is out of the office. It makes us feel more alone with the pain that we need help and can't get it with this. Hopefully he will help you get it under control. It was an arm/ hand surgeon that diagnosed mine when no one else could.
Like Desi, I really believe in people at least getting the blocks. I had 3 and they did put me into remission. You might still deal with some symptoms but it will help deminish the pain. That's what we want, isn't it? I am sorry that you are having to go through this but at least being here with friends you have the great support you need and you will learn so much. Like Desi, I do believe in prayer. I do get angry with God at times but I still know he's walked me through what I have been through. My prayers are with you in this and I will pray for you that these blocks do help you. Ada |
|||
![]() |
![]() |
![]() |
#3 | ||
|
|||
Member
|
I am glad to hear that you have a good doctor willing to help you- so important that a good professional be on your team.
Oh, yes. It definitely is good to know you have "something" because you can try and treat the something instead of sitting around confused. I certainly hear you there- I dealt with that and it is terribly frustrating. ![]() I sure hope the blocks help you out. Sending you some (((pain free hugs))) and of course prayers. ![]() ![]() ETA: I know the feeling... it is so scary when it spreads... hang in there. A good attitude helps. ![]() Last edited by InHisHands; 11-09-2007 at 08:06 PM. Reason: to add more |
||
![]() |
![]() |
![]() |
#4 | |||
|
||||
Member
|
Thank you for your support Desi, Ada and IHH, it means so much to me.
I'm truly grateful I have nice people like you guiding me through this otherwise lonely experience. I also wanted to let you know, I did bring the tingling up to my doctor so he is aware but didnt comment about it. I still havent heard from the Pain Clinic yet, but I hope to soon. Ada, you were one of the first ones to suggest a Pain Specialist to me, so I was pleased when my doctors plan included the Pain Clinic. I'm glad these blocks worked for you, even though it sometimes lasted only a little while. ![]() And Desi, I'm going to ask for Fluroscopy, thank you for that suggestion. I will PM you soon as we definately have a lot to share with one another. I'm going to be as optimistic as possible. I'm still under that 3 year mark everyone has warned me about, right???? I'm trying to get in that "determined" mode where I can say "I have this, it doesnt have me". But I just dont know how to do that when no matter what I do seems to spark a flare up. I'm going to be grateful for what I have, and know that even if my life is nothing but trying to avoid the pain at least I have a life to fight for. Also, I'm going to tackle that laundry that's piled up and even try to make my bed again in the mornings ![]() I'm also going to check back here daily for motivation, assistance, guideance and maybe a few smiles. I'll be sure to kiss my Greyhounds for you all friends! ![]() ![]() ![]()
__________________
myspace.com/asiliveandbreathe |
|||
![]() |
![]() |
![]() |
#5 | |||
|
||||
Member
|
IHH,
I wanted to mention how important your understanding is to me. You've definitely made me feel alot less lonley in the past few days. I think it's so important, especially regarding something which is so uncommon as this, to have people who understand. It really makes a world of difference. Please let me know if there is anything I can do for you in return. ![]()
__________________
myspace.com/asiliveandbreathe |
|||
![]() |
![]() |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
Complete Recovery From Intractable CRPS Type I | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Not convinced of my diagnosis of CRPS Type II | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
new here, new crps? | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Ice and RSD/CRPS | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
recent article showing impaired endothelial function in cold-type CRPS | Reflex Sympathetic Dystrophy (RSD and CRPS) |