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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) |
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#1 | ||
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Junior Member
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![]() So, basically, HELP!!!! Has anyone been in my situation, any suggestions? I really dont know where to go from here. I guess I am getting depressed from all this. I'm not use to just sitting or being in so much pain. I was the one who yelled when people smoked, or took the elevator. My daughter is having my 3rd grandson (she lives in San Diego), and I CANT go there to help and see him. Both of my other 2 grandsons (10 and 4), I saw them at 5 minutes old. I held them, I helped out. Now I cant. This is NOT FAIR!!!!!! lauriegraham View Public Profile Send a private message to lauriegraham Find More Posts by lauriegraham Today, 09:02 AM |
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#2 | ||
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Hi Their,
I want to welcome you here. ![]() |
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#3 | |||
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In Remembrance
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Hi, Laurie:
I don't have RSD, but I do have spinal stenosis in my lower back and degenerating discs. I also have pain in my left leg. It starts in my groin and goes down to just above my left knee. I've been to Pain Management and had an RFA done, to cauterize the nerves in my lower back that are causing the pain. My back feels much better (not 100%, but at least I can get out of bed/chairs without falling on the floor ![]() in pain after the RFA, anyway. I can live with that. ![]() I recently found out that the pain in my groin was a problem with my hip flexor (sp?). So, I'm starting PT again and hopefully things will work out much better than the last time. I also found out that I have some bursitis in my right hip,from the way I walk when my hip flexor acts up-which is most of the time. ![]() Right now, I'm using a quad cane to get around and the Physical Therapist I went to earlier in the week suggested that I get a second one (one for each hand) to help with my balance. I had tried a walker, but it didn't help and the hallways/doorways in this house are too narrow for the walker, anyway. Ask your Pain Management doctor if you're a candidate for the RFA procedure. It really did help me with the pain in my back. If it weren't for the bursitis and the hip flexor, I wouldn't be in as much pain as I am now. Good luck!
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Gina congenital hydrocephalus, porencephalic cyst, epilepsy, lumbar spinal stenosis, degenerative disc disease |
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#4 | ||
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Welcome!!
![]() In was recently dx with RSD, too (dx in Nov. '06).It's hard, but hang in there! ![]() |
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#5 | |||
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Co-Administrator
Community Support Team
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Welcome laurie,
Nice to meet you - I hope we can help, and we can always give support. Sometimes we need to adapt and become type C instead of type A. ![]() But we usually go thru the 5 steps of grief/loss on our way to adapting. Have you had any physical therapy or a evaluation by an expert PT ?{or expert chiro} There are alternative therapies also that might help for the pain- HBOT, Low level laser, TENS... much info is listed our useful sticky thread - http://neurotalk.psychcentral.com/showthread.php?t=247
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Search the NeuroTalk forums - . |
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#6 | ||
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Junior Member
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I was doing physical therapy for 2 weeks. they used different methods to desensitize my thigh (it hurts just to touch it. any clothing or blankets hurts). They did massages (which hurt like hell), TENS, and stretching exercises for my quad and hamstring. When I did these, I couldnt walk for days. I think this pain cam from my surgery site which I think I have instability. But it then agravited my RSD in my thigh. At this point i am not going back. What I am going to do is more research, and then look for specific pain management and pt that specializes in RSD, not just any pain or therapy. I dont think the group I went to really understood what I have and their therapy was not geared to my specific pain.
I just found this website, and I am going to make use of the information and support. I going to be putting specific questions in, but right now, I wanted to just say hi, and thanks for the support. |
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#7 | |||
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Member
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Hey
just wanted to welcome you here - it is a brill site to be part of (though we all wish we weren't here!).I have full body RSD after a fall 5 years ago. Hope that you find the info you are looking for here Rosie xxx
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It's always darkest just before dawn... but smile and the world smiles with you, cry and you cry alone |
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#8 | ||
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Junior Member
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Hi and Welcome,
I have RSD also. I was diagnosed after a sports inquiry and many surgeries to correct, which was corrected, but was left with a somewhat serious case of RSD. I am with an excellant Pain Dr. who specializes in RSD among other pain conditions. I also had a go,go,go type personality before all this, it's hard to get adjusted to. My suggestions is, to seek a Pain Dr. who has experience with RSD. Depending on what part of the country you live in try to seek out teaching hospitals. I see Drs in NYC and also PA. THere are many good RSD doctors just don't go to any Pain Dr. Use the phone don't run around to a lot of appts. To stressfull. If you live on the East Coast of course NYC, Boston Mass-General, John Hopkins-MD,Tampa-FL( I don't know to much about the FL group). In the MID-WESt of course Mayo-CLinic,MN,AZ and FL branches, CLeveland Clinic-OH. I hope this helps. I have had RSD for almost 4 years and I have done a ton of research. I truly wish you the best. Ann ![]() |
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#9 | ||
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Junior Member
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Thanks so much for your responses. Right now I feel like my Pain Mgmt group doesnt really have much experience with RSD. Yes, they tried Nerve blocks (none worked), have me on Lyrica (I think my dose needs to be increased. taking 200 mg twice daily.), also on Kadian. They sent me to pt, which only agravated my pain.
So, does anyone know of a good pain management doctor in palm beach. I live in Lantana. |
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#10 | ||
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Member
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hi laurie,
i feel your pain. i am a 54 year old gramma of 6 boys and i know all about losing the person you were and becoming something you are not happy becoming. i was a very busy icu and post op nuse for years and then came to a dead stop. that was 10 years plus ago and some days i accept it and some days i don't and i think i will always feel that way. we can only adapt and do what we can, some days more than others. your personality will make you more frustrated but it will also give you the push to stay active and fight the good fight. i am glad to meet you and hope you find some help and support here. joan ![]() |
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