Complex regional pain syndrome
Posted , 24 users are following.
My son has had spontaneous onset Crps for the last 5 years and it affects his left foot making walking very difficult and the whole of his right arm from fingers to shoulder. He has tried numerous treatments with no improvement and is to ill to work. He lives in supported housing with a carer for support. I would love to speak to any other person who is in this position. I live in the uk
3 likes, 63 replies
violetb sandra291
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1. it is often times the case that CRPS strikes for no reason. I know it's crazy.
2. I have CRPS as a result of surgery, but weeks and weeks later it just appeared.
3. I have been on gabapentin for 5 months now and started almost immediately when the pain started. I have definitely had improvement on the 'hot' side of things. My foot usually does not get hot enough to fry an egg on anymore, but feeling extremely stiff, cold, numb, pins and needles continues non-stop.
i feel so sorry for your son. I feel like a shadow of myself, but I am 63. I sure hope your son does not have to live with this condition.
Anyway, if your son isn't on gabapentin (neurontin) then suggest it to your doc. other drugs that work for some are: lyrica and elavil (amitriptyline hcl)
Good luck
sandra291 violetb
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carol91733 sandra291
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eva96035 violetb
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linda43575 sandra291
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carol91733 linda43575
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Cillasmum linda43575
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diagnosed myself I too looked it up on the Internet and was heartbroken. However a lot of people do recover in time so please stay optimistic. Like
you I was very active before this happened always at the gym and used to swim 150 lengths a week. You may also be prescribed Gabapentin over the next few weeks and referred to a pain management clinic if symptoms persist. I was quite worried over meds prescribed but I am bearing with them as I just want to get better. In fact I have noted a slight improvement in my hand and the meds have taken the edge off the pain. So onward and upward! Please let me know if I can help in anyway, if I was near I would be giving you a Big Hug x so keep your chin up and let me know how things are going
sandra291 linda43575
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Cillasmum sandra291
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elaine_2770 carol91733
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linda43575 Cillasmum
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I have seen 2 different physios, ( NHS) the first of which had no knowledge of the condition, and basically told me to rest, relax and not be anxious. And not to try to use my hand. He has moved on, and I am now seeing a lovely lady once a week. She spends time massaging my hand and manipulating my wrist and she said I should use my hand and could get back to exercise.
So I have been to Boot Camp twice! I can't do a lot of the things I could (obviously press ups are out) but am enjoying being out in the fresh air, with good friends rather than sitting moping and watching Judge Judy!
i see the orthopedic consultant in 2 weeks, and my referral to the Pain Clinic is in June. Ridiculous amount of time to wait.
i feel I am gradually getting my life back and there is a lot of hope where there was despair.
elaine_2770 linda43575
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carol91733 linda43575
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debbie26552 linda43575
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maddy1234 linda43575
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