Anyone else here have or had a pain pump?
I have one, coming up on a year now. Before I go into a TLDR on the subject, I'd kinda like to know if there's a group of "fellow travellers" out there. I'm more than happy to share my story, but I know it's really a nich kind of solution that's not for very many people.
Hi,
!
I know some of our members have experience with pain pumps (specifically, Baclofen pumps, if I remember correctly) and I will link some of their stories/discussions. However, I am always open to learning more about this type of pain management, as I don't have any personal experience with it. Please do feel free to share, though don't feel obligated.
In the meantime, I wanted to share this brief discussion on the topic of pain pumps -- https://multiplesclerosis.net/forums/baclofen-pump. And here's another discussion from our forums on this topic -- https://multiplesclerosis.net/forums/severe-spastisity-looked-like-breakdancing. And, yes, here's ANOTHER discussion on morphine pumps -- https://multiplesclerosis.net/forums/morphine-pump. So, this topic does come up here, but we could definitely use some fresh input!
Best, Erin, Team Member.
