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DiscussionNerve biopsy test: Is it done by a neurologist or rheumatologist?
Neuropathy | Last Active: Dec 10, 2021 | Replies (222)Comment receiving replies
Replies to "HI JIM. I'm new to this reading your post I wonder if the recliner isn't part..."
@catharbert Thanks for writing. I do see a therapist every week, and have been for 14 years. Pain when sitting is pretty much the same, whether it's in a dining chair, a recliner or driving the car. If I walk very long, my feet and ankles will begin hurting more the longer I walk. We have a big place, even though 8 of the 10 acres are in use as pasture for our neighbors' cows and horses, and I'm really thankful for my riding mower.
I have the same approach to sleep position as you. I use a Bipap machine because of sleep apnea, so I usually sleep well if pain doesn't wake me up. I put a pillow between my knees because if they touch, it sends pain signals to my feet, and if I lie on my back, my heels will start hurting.
It took a few years to find the antidepressant that works, and I've been taking it, Wellbutrin, since the end of 2005. So far so good. My doctor prescribed morphine sulfate contin 8 or 10 years ago for the pain in my feet, and it's the only medication that's helped long term. I've tried one medication after another, and some have helped, but only for a month or two. I had a spinal cord stimulator implant in 2017, and it was wonderful! I'd forgotten how it felt not to be in pain. It gave me pain relief for a year. The surgeon has said that stenosis surgery could help enough to allow the stimulator to do its job again. I'll know in a month.
Again, thank you for writing.
Jim
@catcando @rwinney @jimhd Wow, here I've been over in other discussions the past couple hours doing my usual catch-up on the Daily Neuropathy News, when the real action was happening over here. Rachel, you are never up now. Wow!
My deepest most earnest sympathy and sorrow for you guys and what you are describing about your lives, both with your pain and with family who just can't seem to "get there" when it comes to the deepest understanding of what you are going through. I have none of what you go through. As much as I try to "be there" for you guys, and, of course, for my wonderful spouse, I can't sustain it. I forget. I do. I am solicitous as I can be, like Kevin Rachel, I'm like "do you need this?" "can I do that for you?" etc. But I am one who likes to keep it light, wanting to be humorous, I just can't keep the pain you all are experiencing in the forefront of my mind all the time, but yet you are experiencing it all the time. It must be a rare person that can be there ALL the time. I just try to be available. I am always ready to pour it out as Linda indicates a need, but it sure is easy to forget if she' not giving me the cues.
I feel very deeply when I feel. But that too gets exhausting. Ugh, nothing about neuropathy is GOOD. I'm sick to death of having to know how bad it is for you guys and I can't do a damn thing. Sorry.
@catcando, you seem like a really great person and I am sad for your pain also. The only thing I'd say about your post (besides thinking how nice you sound, and caring) is just go and read a few of Jim's recent (last couple weeks) posts to get a sense of his experiences with depression. You can see them by clicking here @jimhd ; he has been through it, this man has, and then some. I have fallen head over heals in love with him and with Rachel and with all of the people here. It came unexpectedly right out of the blue since January when I joined.
OK, sorry you guys. I'll go take a walk and try to stabilize. Best to you, Hank
PS: I just proofread this. It's not saying enough. It will have to do.