What is RSD and what are the symptoms of it
Reflex sympathetic dystrophy syndrome (RSDS) is a condition that features a group of typical symptoms, including pain, tenderness, and swelling of an extremity associated with varying degrees of sweating, warmth , coolness, flushing, discoloration. [ Source: http://www.chacha.com/question/what-is-rsd-and-what-are-the-symptoms-of-it ]
More Answers to "What is RSD and what are the symptoms of it"
- What is RSD and what are the symptoms of it
- http://chacha.com/question/what-is-rsd-and-what-are-the-symptoms-of-it
- Reflex sympathetic dystrophy syndrome (RSDS) is a condition that features a group of typical symptoms, including pain, tenderness, and swelling of an extremity associated with varying degrees of sweating, warmth , coolness, flushing, discol...
- How long after a trauma do RSD (crps) symptoms .
- http://search.healthcentral.com/query?q=crps&st=s&x=1&y=1
- How long after a trauma do RSD ( crps ) symptoms begin? answers (3); RSD now known as CRPS -1, Can it "burn itself out", as one doctor we know is alleging? http://www.healthcentral.com/chronic-pain/c/question/745077/72871
- Does anyone know of anything that would cause RSD type symptoms??
- http://pape-chi-ro.blogspot.com/2009/12/rsd-more-conditiontreatment-does-anyone.html
- I was diagnosed with RSD by several doctors. However, a physician who is an expert RSD said that I do not RSD. He said he had a few more tests that have no money.
Related Questions Answered on Y!Answers
- Will nerve blocks help with full body RSD?
- Q: I've had RSD/CRPS in my left foot for about a year, but recently it spread to my other foot, and lately I've been experiencing very RSD-like symptoms in my legs and upper body. My current doctor doesn't think so but I think he may be wrong (nobody seems to know enough about this disease, even specialists, so I don't trust any of them). Anyway, he's pushing me to get nerve blocks. But, if I do in fact have RSD in my upper body (albiet in mild form so far), would that do any good? If its in my whole body, won't blocking off just one part not help? Could it make it worse, since it's an invasive procedure?Also, what treatment options would be open to me if I do in fact have full-body RSD? To nip it in the bud?
- A: If you have full-body I would say that the block wouldn't help the all over body pain, but it may help a certain portion such as a leg or foot feel better. Nerve blocks aren't all that invasive, basically they just insert a small needle into your back, but it certainly could still cause problems with the RSD/CRPS. A few things I would recommend for full body would be a low dose ketamine infusion, or hyperbaric oxygen therapy. Spinal cord stimulators are another option, but they won't treat full body RSD. Pain pumps are an option, but should be used as a last resort. Unfortunately there is no real cure for the pain so every treatment reacts differently with different patients. Good luck and feel free to e-mail me if you have any questions.
- Will a nerve block help with full-body RSD?
- Q: I've had RSD/CRPS in my left foot for about a year, but recently it spread to my other foot, and lately I've been experiencing very RSD-like symptoms in my legs and upper body. My current doctor doesn't think so but I think he may be wrong (nobody seems to know enough about this disease, even specialists, so I don't trust any of them). Anyway, he's pushing me to get nerve blocks. But, if I do in fact have RSD in my upper body (albiet in mild form so far), would that do any good? If its in my whole body, won't blocking off just one part not help? Could it make it worse, since it's an invasive procedure?Also, what treatment options would be open to me if I do in fact have full-body RSD? To nip it in the bud?
- A: Hi Tony,If indeed it has spread like you think, there is probably less chance of the blocks working well because that indicates that it's becoming more centralised. However, I'd also say that there is never any harm in trying because a/ everyone responds differently to different treatments and b/ blocks are relatively non-invasive. I would recommend that you discuss a ketamine infusion with your doctor. Ketamine is actually a general anaesthetic drug, but is used as a low-dose infusion to treat CRPS/RSD pain - often with good results.If you don't mind me asking, are you on any medications? Are you doing any physiotherapy? If not, it's vital that you do - you need to keep your affected limbs moving as normally as possible and not allow yourself to develop any guarding behaviours due to the pain. Seeing a good physio (one who has some knowledge of CRPS) at this stage, if you aren't already, may also help to prevent any progression in your upper body. I've got severe full-body CRPS - arms, legs, my back and other complications as well. Been through just about every treatment there is, so if you've any questions feel free to email me.
- Here are symptoms, what is diagnosis?
- Q: Symptoms include: RSD, cubital tunnel syndrome, several herniated discs in lumbar and neck, diabetes2, glaucoma, neuromas, extreme skin changes (ie- has become mottled, changes texture and color, may be red or gray, temperature avg 101.2 most days, very bloated abdomen that is very hard like a rock (looks very pregnant), extreme pain in bones, joints. Very swollen lumps, size of half an egg on wrist joint, elbows, etc. Elbow on L feels like a hot screwdriver is poking inside it each time it is moved (x-rayed, no fractures), easy bone breakage of toes, back of hand and fingers, losing hair rapidly, aged rapidly over 5 years (when this started with broken toes that couldn't heal). Fatigue, RLS even in daytime and in arms as well as legs, several times a month. Vitamins/minerals/herbs, physical therapy, Rx drugs have not helped much. Have always been vegetarian and eat organic, whole foods. Drink at least a gallon of water a day. Always feel too hot, love in the 50s. Need fans, ice caps.I go to lots of specialists, including a relatively famous pain clinic. I have had surgeries, blocks, am on a few narcotics and other meds. In physical therapy. Will start a tens unit soon. I just wanted a fresh take from other eyes that have maybe seen something similar to this before. :-)I am 58, way passed menopause. I have been extremely healthy and active - hiking, biking. Was a motivational speaker and teacher as well as artist. This was a sudden hit. (blah!)
- A: Could it be sarcoidosis? This is an auto immune disorder that can affect all organs and produce many of your symptoms. It is also one of those which can be easily misdiagnosed. It definitely sounds like an auto immune disease to me, your body is attacking itself, so to speak, and there are several which produce similar problems and symptoms. Have your Docs looked in that direction at all? Also, please ask your doctor about Hyperbaric Oxygen Therapy for your RSD. This is an FDA approved therapy that has shown incredible results and relief for the many who utilize it. Your only alternative is pain management and you already know that doesn't always work that well and could be making you feel worse in other ways. Many of your symptoms of course are related to the RSD. Skin changes, temperature, swollen and painful joints with no positive x-rays, fatigue, and so on. All of these are classic RSD, which I believe actually started as a reaction to your carpal tunnel syndrome first, and the rest followed as the RSD spread to other areas. Above all else, I wish you better days ahead. The onset of RSD is very sudden and the road back a slow one. My thoughts are with you.
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