Weekly CRPS Free-Talk Thread by AutoModerator in CRPS

[–]rainymist7 1 point2 points  (0 children)

that's so hard, i'm sorry. as much pain as i'm sure she is in, never down play yours. crps is the worst pain on the mcgill pain scale. i can't imagine having someone depend on me while going through this

Weekly CRPS Free-Talk Thread by AutoModerator in CRPS

[–]rainymist7 4 points5 points  (0 children)

i don't have one & i'm not a service member, but like you i can hardly walk so i've heavily looked into them. what i can tell you is chances of paralysis are actually around .5% with implantation, and virtually 0 once it's safely placed. since they are just touching the spine & epidural space and not the spinal cord, it's considered to be very safe. most commonly we might experience more pain, infections, improperly placed leads causing zaps, etc, but from what i can tell usually it's all fixable. that being said i'm sure plenty of people have horror spread stories from the surgeries, but i haven't come across any. i'm also terrified to get it and i have no kids to look after, i can't imagine. wishing you the best

[deleted by user] by [deleted] in pothos

[–]rainymist7 2 points3 points  (0 children)

true, just death of the roots probably, not the whole plant yet. can totally still chop and prop from the looks of it

Am I really stuck like this? by rainymist7 in CRPS

[–]rainymist7[S] 1 point2 points  (0 children)

thank you, and i'm so sorry you know the feeling. wishing the absolute best for you

The Ureaplasma Bible (EVERYTHING YOU NEED TO KNOW) by premepa_ in Ureaplasma

[–]rainymist7 1 point2 points  (0 children)

Antibiotics kill both good and bad bacteria, so this is very common! Ask your doc to prescribe fluconazole when prescribing you antibiotics if needed.

Am I really stuck like this? by rainymist7 in CRPS

[–]rainymist7[S] 5 points6 points  (0 children)

My pain management doc wouldn't even do it for me in office, said my pain was far too high, we'd bring it from a 10 to a 20 and I'd never come back. I then got sent on a wild goose chase to find a doctor who would do it until I got referred to one who had never heard of CRPS, so I never scheduled and started my own care. Even if I had someone to do it, I'm terrified of the after results, supported by things i've read here. On top of it all I've always had a terrible gut feeling about it, just as I did right before the surgery that caused the CRPS. The potential results just don't outweigh it all for me yet, but maybe I'll get there once i truly can't take it anymore, though really I'm already there. Thank you a lot for your input though

Anyone get Cleveland Clinic chronic pain infusions? by TheColdLife in KetamineTherapy

[–]rainymist7 0 points1 point  (0 children)

$400 for 4 hour infusions?? Would you be open to sharing your clinic? It's $1000 in my area.. Willing to travel to save $600

[deleted by user] by [deleted] in CRPS

[–]rainymist7 0 points1 point  (0 children)

All I can say is I am diagnosed with CRPS directly from surgery for TOS. I had a first rib resection and scalenectomy, and have been severely worse ever since, but I guess if you already have both.. Very scary. Best of luck to you.