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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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After a year and a half I finally have a job. It is an easy job. I am working at a nursing home as an activity assisstant.
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#2 | ||
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Member
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Im glad to hear of your good fortune,,Its nice when we are able to be able to work,,,,take care and enjoy the freedom that the lord has given you,,peace is a good thing
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#3 | |||
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Junior Member
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I know how excited i felt when i got a job after my injury.. Just be extra careful not to rehurt yourself.. I dont want you to get worse... I am so happy for ya.. The elderly dont understand that you hurt too.. So just take your own precautions too ok..
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Barbara |
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#4 | ||
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Good luck- Iam jealous-Wish I could work!!!
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#5 | ||
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#6 | |||
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Senior Member
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Congrats! That is great news! I hope it goes well for you.
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#7 | ||
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Senior Member
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Congrads !
I'm going to second Babs warning......just be careful not to over do it ! |
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#8 | ||
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Magnate
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Wow I am so happy for you. I hope for this day too. May I ask is this the type of job you did pre rsd? The reason is when I was feeling better I was thinking of things I could do with the limits I have plus the fears of getting hurt.
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#9 | |||
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Member
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That is wonderful....I used to work as a CNA and it was HARD, but activity assistant sounds really fun
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"Thanks for this!" says: | Wilbyfree (03-29-2010) |
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#10 | ||
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Junior Member
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Thank you all. No this is not what I did pre RSD. I worked mostly fast food. I too was wondering what I could do with the limitations. I was volunteering there for like 6 months then one day the old activities assisstant just walked out. Because I always showed up earlier than what they said I had to and would be there later than I had to they offered me the job. It is a very fun job. I love it. I do becareful so I do not hurt myself worse. It took me a while to figure out how to push the residents but I have it all figured out. I have only mentioned a couple of times that I have this disease to the residents. I know they are suffering enough and do not need to hear my problems on top of it all. When I do have a bad day I try to distract it by talking about other things with them or the other ppl that work there. Sometimes it works and sometimes it don't so I just grit my teeth and try to keep going but it slows me down. The most embarassing part of it all is the sweating. Where this goes from fingertips up the right arm up the neck and down the back I have horrible sweat in the right arm pit. So I just keep my arm down when around ppl so they dont see. I need to see if there is some sort of pad I can put there for extra protection. My step mom suggested I try a mens deodorant and see if that would help me out. I have tried all the womens and the only one that seems to do even just a little bit of good is the Degree Clinical Strength. Do any of you have any suggestion for this? And I'm sorry it took me so long to write back just have been busy.
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"Thanks for this!" says: | Kakimbo (03-29-2010) |
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