Guest guest Posted January 9, 2008 Report Share Posted January 9, 2008 Hi . I just joined two days ago and I understand the shoulder pain. My doc told me to do stretching excersise's and to use a pilate's band for some resistance. I just got shots of cortizone in my shoulders and will start the stretching in a couple days to allow the med to work before I use my shoulders like that. I am hoping that this will help with some of my stiffness/pain in my upper body. Good luck. Question: when you have done therapy before have they given you papers showing you how to do excersises at home on your own? The last therapy I went to gave me some and that is what I will use to get started again. Christi Randall www.singingwomenoftexas.com want to reintroduce myself Hi to everyone. MY name is I joined in the beginning of Dec. but my fibro has been so bad I have not been able to answer. Thank you to those of you who so nicley welcomed me. And to ansewer the question about my shoulder. Yes it is from the fibro and loss of movement we all have. The pain was so severe in my shoulder I just could not raise my arm on a regular basis as I should have. Now my right one is trying to do the same thing. Therapy is essental for all of us to maintain our range of motion but how many can go on a on-going basis? It is too expensive. So I am trying to make efforts to move them more but it is soooo hard!! I share with all of you the pain and loss of parts of our lives like work, and play. Sometimes I find it so unbeliveable how fast everything has changed. 1. While it is wonderful to share our experiences with everyone on the list as to what treatments do and don't work for us, pls always check with your dr. Some treatments are dangerous when given along with other meds as well as to certain health conditions or just dangerous in general. 2. If you are in a difficult situation (doesn't matter what it is) pls don't be afraid to ask for help. It is the first step to trying to make that situation better. 3. To unsubscribe the e-mail is: Fibromyalgia_Support_Group-unsubscribe 4. Also, it is not uncommon for more than one member to be feeling bad at the same time when it comes to flares and b/c of that potentially take something another member says the wrong way. And that includes the things that one member may find funny (even if it's laughing at fibro itself) even though we who deal with illness whether one such as fibro or multiple illnesses try to keep a sense of humor. 5. Pls let's be gentle with each other, and if you are having a bad day pls let us know so that we can do our best to offer our support. Have a nice day everyone. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2008 Report Share Posted January 10, 2008 >Hi , I just joined the group this week and love it, everyone is so nice and caring. Your right it does get expensive and the insurance only pays for so many visits half the time. What I found to work (and I do this with my husaband and myself) is we have a work out time, What I mean is I asked the OT, PT, and ST what we could do at home and they all gave me sheet of papers that had easy to do work outs on them so we try and do a few each day. Speech is for my husband but ot and pt works for both of us, lol. I have pain in my shoulder and the one thing the ot had me doing is (sound strange) walk my fingers up the wall and back down I guess it streches the rotorcuff to help with range of motion. Hope this helps alittle. (((HUGS))) Tina > Hi to everyone. > MY name is I joined in the beginning of Dec. but my fibro has > been so bad I have not been able to answer. Thank you to those of you > who so nicley welcomed me. And to ansewer the question about my > shoulder. Yes it is from the fibro and loss of movement we all have. > The pain was so severe in my shoulder I just could not raise my arm on > a regular basis as I should have. Now my right one is trying to do the > same thing. Therapy is essental for all of us to maintain our range of > motion but how many can go on a on-going basis? It is too expensive. So > I am trying to make efforts to move them more but it is soooo hard!! I > share with all of you the pain and loss of parts of our lives like > work, and play. Sometimes I find it so unbeliveable how fast everything > has changed. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2008 Report Share Posted January 10, 2008 > And to ansewer the question about my > shoulder. Yes it is from the fibro and loss of movement we all have. > The pain was so severe in my shoulder I just could not raise my arm on > a regular basis as I should have. Now my right one is trying to do the > same thing. Therapy is essental for all of us to maintain our range of > motion but how many can go on a on-going basis? It is too > expensive. So > I am trying to make efforts to move them more but it is soooo hard!! I read this, and Debra V's response. I have the same kind of problem. I had physical therapy for it back in 1999, I think. A couple of months ago I dug out my old exercise sheets from that go- around and very gently started up the same physical therapy exercises that I got back then, and have been adding a few. I also started playing my cello again. The first few times I played it, my shoulder would seize up and flare and I couldn't hold my right arm up. I slacked off during the holidays, and things started hurting again, but I'm back at it. As long as I do the exercises, it seems to help,and while the pain isn't *gone*, it's better, I have more range of motion, and seem to be building some strength. Plus I can play my cello longer. Have you talked to your doc? It could be that with a few physical therapy sessions, they can help you develop a plan for ongoing exercises to help build strength and keep it from getting worse. I always say that people like me don't exercise, we do physical therapy. ;D Z Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2008 Report Share Posted January 10, 2008 Well, hello again, . Sorry to hear about your awful shoulder pain. I hope that belonging to this group is helpful to you. At least you know you are not alone and that at least WE care. Jeanne in WI > Hi to everyone. > MY name is I joined in the beginning of Dec. but my fibro has been > so bad I have not been able to answer. Thank you to those of you who so > nicley welcomed me. And to ansewer the question about my shoulder. Yes it > is from the fibro and loss of movement we all have. The pain was so severe > in my shoulder I just could not raise my arm on a regular basis as I > should have. Now my right one is trying to do the same thing. Therapy is > essental for all of us to maintain our range of motion but how many can go > on a on-going basis? It is too expensive. So I am trying to make efforts > to move them more but it is soooo hard!! I share with all of you the pain > and loss of parts of our lives like work, and play. Sometimes I find it so > unbeliveable how fast everything has changed. Quote Link to comment Share on other sites More sharing options...
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