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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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Community Support Team
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yes, this thread is 2 years old and sadly I also noticed a spam affiliate signature
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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#2 | ||
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Junior Member
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I am always sorry to hear of anyone so young having to deal with this monster called RSD, my heart goes out to you. After reading yours and other posts I am wondering if you could tell me how long ago you were diagnosed. I too am very surprised that they have not tried blocks on you, and would surely recommend it. As for what your doctors say about your career being kaput....All I can say to that is don't take to heart what every doc says. Some of them can be very insensitive and they don't realize that they can create self-fulfilling prophecies. I was diagnosed with RSD when I was 24, and at that time I was told I would not walk again. I do walk most days and I also chase after two young children - I sometimes have to do things differently than other people, but my children are happy, healthy and well adjusted and tearing up the house as we speak. I had just started my career at the time RSD hit and had a great job as a counselor in a Toronto Hospital....yes, that career was over. Now I volunteer helping counsel troubled teens and run a support group - it is much different than what I planned on, but rewarding in its own way. To the next doctor that makes a remark like that to you - well, I have found over the years it is always very satisfying when I can throw something back at them - like 'thank you for your opinion, but right now I am focusing on what I can do.' Keep pushing for treatment my friend, there are many out there that are worth trying and have helped tremendously for some people...just always research them a bit first if you can. I am sure that there are a lot of caring people here that can help answer questions too. Hang in there my friend!
Gentle huggs Kimberly |
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#3 | ||
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Member
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Hey Kes. Glad to meet you. Sorry it is meeting bc of rsd/cprs but yeah.
Im nikki. i am almost 16. im in south carolina. i was diagnosed when 14 after a minor break to the ball of my foot when i landed wrong in gymnastics. my rsd is almost full body. have you tried lidocaine/lisoderm patches? i havent yet but i have heard that they help and i dont like taking lots of pills. too much 4 me to remember. cool! syracuse is really close to my grandparents. |
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#4 | ||
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Junior Member
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hello kes, i am only sixteen years old and have had rsd from my legs up my back for six years. i am currently walking with a cane and using a wheelchair for long distances. i recommend you find the best PM doctor in your error, have you tried spinal blocks. i would do PT, and start a desensitization program. i am on amitriptalyne 50mg. it helps me relax at night. nice to meet you
good luck taylor |
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#5 | ||
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Member
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Hi Kes,
I am so sorry to hear about you having RSD. You are so young it is a lot to deal with. I also did not have swelling or an initial injury and was dx'd about a year and a half ago. I agree with the other posts keep looking for a treatment that will give you some relief. I have had ketamine and will be getting more treatments. I have used lidoderm patches on certain areas and they did help. Most of all do not give up your hopes and dreams. You have a long life to live yet and I'm sure it holds many good things for you. Kepp coming back to this site. There are a lot of good people on here who have given me encouragement when I lose faith. hopeful |
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