Oof. That sounds awful. I also understand how that would happen. My damaged nerve services the lower portion of my abdominal cavity, groin, and upper thighs, so I tend to have problems dismissing gastrointestinal issues. A couple years ago, I suddenly became super distended. Like a skinny guy with a basketball under his shirt. It turned out that I had an intestinal intususpeption that basically closed off my tract and inflated me like a balloon. I would’ve noticed the pain way earlier if I didn’t have jumper cables on my nuts. Lol
It’s amazing how little neurologists are willing to commit to certainty of any kind. I’ve gone to several, and all I get is speculation and hope. Has your wife had the same experience?
Yeah, similar. She has CRPS, and they just don’t understand that very well. Since it’s neuropathic, most drugs don’t do much and she doesn’t like the side effects anyway. They used to call it the suicide disease because so many people would just kill themselves rather than deal with the unending, untreatable pain. Treatments have gotten somewhat better though. Still, most doctors don’t know what to do with her.
I just looked it up. It sounds awful. I’m sorry she has to deal with that, especially having so little information. I’m frustrated with the level of support I get for my trauma, but at least they can give me some definitive understanding of the mechanics. I really hope they learn more about her condition.
Oof. That sounds awful. I also understand how that would happen. My damaged nerve services the lower portion of my abdominal cavity, groin, and upper thighs, so I tend to have problems dismissing gastrointestinal issues. A couple years ago, I suddenly became super distended. Like a skinny guy with a basketball under his shirt. It turned out that I had an intestinal intususpeption that basically closed off my tract and inflated me like a balloon. I would’ve noticed the pain way earlier if I didn’t have jumper cables on my nuts. Lol
It’s amazing how little neurologists are willing to commit to certainty of any kind. I’ve gone to several, and all I get is speculation and hope. Has your wife had the same experience?
Yeah, similar. She has CRPS, and they just don’t understand that very well. Since it’s neuropathic, most drugs don’t do much and she doesn’t like the side effects anyway. They used to call it the suicide disease because so many people would just kill themselves rather than deal with the unending, untreatable pain. Treatments have gotten somewhat better though. Still, most doctors don’t know what to do with her.
I just looked it up. It sounds awful. I’m sorry she has to deal with that, especially having so little information. I’m frustrated with the level of support I get for my trauma, but at least they can give me some definitive understanding of the mechanics. I really hope they learn more about her condition.
Thanks, me too!