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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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Hi everyone,
I had surgery on Monday to get the scs out. Now the lead that was sitting on a nerve is gone and the battery that kept moving and pushing against my skin. Everytime it rained or it was damp outside the pain was off the charts. I am hoping noe that its gone this will be one less pian to deal with. Except for the pain from the cuts and the sleepiness, I am felling pretty good. Its also nice to be wsited on by my hubby. I think I'ii try to carry that out a bit longer. I hope everyone is well. Sue K |
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#2 | |||
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Hi Sue..
I hope this removal makes a huge diffrence for you.. seems all of the treatments work diffrently for each of us.. sometimes what works so well for one is considered invasive by another body.. I am glad you got it out in time to enjoy the holiday season more than you would have.. myself I will just be glad to spend christmas at home this year instead of hospital ![]() Happy holidays bud, Sandra |
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#3 | ||
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Good luck.
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#4 | |||
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Hi ya Sue!! Good to see you. I feel bad.. so bad for you!! Good to see you.. and YES have that hubby of yours wait on ya, sweetie!! LOL Love ya!! ~Desi
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I Will Always Believe in Poems, Prayers And Promises Love, Desi . |
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#5 | |||
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Sorry to hear that things didn't go well with the SCS. What works for some doesn't work for others.
Hope you start feeling better soon. Ada |
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#6 | |||
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Hi Sue K,
I am so sorry about the problems you have had with your SCS. I hope that you start having low pain days now that the SCS is out. Take care Pain free hugs Love Alison
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To the World you may be one person, but to one person, you may be the World. |
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#7 | ||
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I Just Talked On The Phone To My Hip Sister Sue And She Sounds Tired But Good. I Am Relieved That Here Scs Came Out And That She Had No Complications From That Procedure. She Is A Very Special Person. So, Love To You Sue!!!! Joan
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Courage ... doesn't always roar, sometimes courage is the quiet voice at the end of the day saying, "I will try again tomorrow." |
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#8 | ||
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Thank you Joan. I was so happy to talk to you. Love you too.
Sue |
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#9 | ||
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Quote:
Thanks for your post. I am considering getting my SCS removed as well. Not only has it lost effectiveness over time, but now it is really pushing against my skin. I lost over 45 lb since the generator was installed, and no longer have "all that padding" in the hip area. I wear a lidocaine patch over the SCS daily. It feels like I am sitting on a rock. The lump is now quite noticible and when I fly the TSA screeners are sometimes very suspicious of the hard object. (I am not complaining about that - I am glad they are cautious.) I hope you will be glad you decided to get it removed. No sense continuing with something that is causing more pain or even discomfort. We all get enough of that as it is. Mike |
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#10 | ||
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Member
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Mike,
Mine was also pushing on my skin. It felt like it was going to come right through. The lead sitting on the nerve was also very painful. I feel so much better with it out and taking it out was so much easier than when they put it in. It sounds like you would feel much better with it out. Take care. Sue |
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