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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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Good Morning All,
I was diagnosed with RSD on New Years Eve by a hand surgeon who I went to after I started to get burning pain in my hands. I had been seeing a neurologist for a bad concussion I had received a year ago and he thought that the burning might be a symptom of my concussion. I only had the one symptom,the burning pain but starting yesterday and continuing today my hand has a blotchy red color to it.I will try to attach a photo . If anyone could give me their opinion if this is what they mean by color change as a RSD symptom I would appreciate it. thank you, Joe |
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#2 | |||
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Member
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[QUOTE=joby7165;1053363]Good Morning All,
I was diagnosed with RSD on New Years Eve by a hand surgeon who I went to after I started to get burning pain in my hands. I had been seeing a neurologist for a bad concussion I had received a year ago and he thought that the burning might be a symptom of my concussion. I only had the one symptom,the burning pain but starting yesterday and continuing today my hand has a blotchy red color to it.I will try to attach a photo . If anyone could give me their opinion if this is what they mean by color change as a RSD symptom I would appreciate it. thank you, Is there pain too?It looks blotchy like my leg gets..But you may also have something pinched..Does it feel knub? I pulled a muscle about 3 months ago and I had pain all down my neck,arm and fingers.It also turned colors..So keep track of what happens.Write it down..Like even if weather is bothering it..Using it,Sharp pain,knubness,ect..If it is rsd,do not use ice..Use heat only..good luck..Hope you feel better soon.. |
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#3 | |||
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Member
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Yes, it does look mottled red. Like moosey said, keep track of descriptions of the pain & other changes like shinyness, thining skin, nail changes. NO ICE if
it's RSD. Keep it moving gently all you can.
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RSD/CRPS and contracture of left hand and arm after surgery for broken wrist. |
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#4 | ||
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Senior Member
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Definitely keep a diary of your pain, symptoms, temperature and colour changes - they are exactly that - the changes in skin colour and temperature that happen in that area alone, not your whole body, or both hands as a result of being outside for example. Take photographs of anything unusual you see and take everything to your next appointment. Doctors love these kinds of records.
Bram.
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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! . |
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#5 | ||
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Junior Member
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Thanks for all the input. The other issues I had was severe swelling in my right foot and lower leg,will include another photo.Once the hand specialist diagnosed me with RSD I have been reading everything I can about the disease.
I do have the shiny like appearance on my fingers of both hands. I have the same symptoms on my left hand just not as severe.Also,my skin feels like rice paper.Every once in awhile I'll get a severe electrical like shock in my hand.The joints in my hand are very stiff,I can open my right hand completely with extreme difficulty but I can't close it into a fist.The nail growth is pretty weird as well,growing much quicker than usual.It is pretty bizarre to get diagnosed with such a strange condition with so many strange symptoms to only start crossing off so many of them in my head. The hand specialist recommended occupational rehab which I did for three sessions before workers comp denied it saying that it wasn't associated to my fall from work so I've been doing the exercises at home trying to hold this at bay but it seems to be getting just a little bit worse every day. Joe |
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#6 | |||
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Member
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Quote:
But anyway keep track of everything and who you saw,and what you had done..Very important...Good Luck |
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#7 | ||
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Junior Member
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Thanks for the good advice Moosey, I will definitely keep track of everything
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"Thanks for this!" says: | moosey2me (02-26-2014) |
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#8 | ||
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Junior Member
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#9 | ||
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Junior Member
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Thank you Tullis, your situation and results have given me hope since my neurosurgeon told me that my neurologist would probably recommend ganglion blocks to me but my biggest fear is my second treatment of botox for the awful migraines I've had since my concussion last January but I'm going to bite the bullet and get the botox,I can't take these headaches much longer.
thanks again! ![]() |
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#10 | ||
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Junior Member
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