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-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Bad flair up (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/255538-bad-flair.html)

RSD31 05-15-2020 07:37 PM

Bad flair up
 
Can’t deal with this live on border in Canada my RSD is work related US side an Can’t get across the border it is shut down an I need to go to hospital but the hospital is dealing Cov -19 **** and I don’t need that too. my pain has been a 10 for the last 3 days and I’m going’ out of my mind I’m hiding in the back bedroom because I can’t deal with this anyone.

annabanana123 05-19-2020 07:12 AM

I'm so sorry you're dealing with this! Do you have a pain management doctor you can call? Do you have any meds you can take for it? Or medical marijuana or anything? I hate the bad flair ups...it's like nothing works except massive doses of meds and even that doesn't always help that much. Hope you're feeling better soon.

RSD31 05-19-2020 09:07 PM

I went to hospital an got a couple of pain shots pain doctor wants to admit to hospital for a couple of days.

CRPSbe 05-24-2020 04:25 AM

Quote:

Originally Posted by RSD31 (Post 1286498)
I went to hospital an got a couple of pain shots pain doctor wants to admit to hospital for a couple of days.

I'm glad you got some help. Keep us posted! Hang in there!

annabanana123 05-26-2020 07:49 AM

Quote:

Originally Posted by RSD31 (Post 1286498)
I went to hospital an got a couple of pain shots pain doctor wants to admit to hospital for a couple of days.

How are you doing now? What is your treatment plan going forward? I think we're all always looking for ways to improve our own

RSD31 05-31-2020 12:07 AM

Katamine
 
They want me too do. The katamine infusion but my wife an daughter are not happy with what they have read about it I would love to talk to someone who has done it the problem I think for me is I’m 42 years this June with this RSD and I think I,m running out of thinks that will help me because I,m having problems with kidneys and other organs because of the RSD and the long term use of Rx’s.

annabanana123 06-01-2020 07:22 AM

Quote:

Originally Posted by RSD31 (Post 1286713)
They want me too do. The katamine infusion but my wife an daughter are not happy with what they have read about it I would love to talk to someone who has done it the problem I think for me is I’m 42 years this June with this RSD and I think I,m running out of thinks that will help me because I,m having problems with kidneys and other organs because of the RSD and the long term use of Rx’s.

I'm sorry! What about the ketamine are they unhappy with? I would try it in a heartbeat if my insurance was willing to pay for it. Also which meds messed up all of your organs? My understanding is some are worse than others and I'd like to avoid what I can...praying you get some clarity and can reach the same page as your family on what the best next steps are.

RSD31 06-02-2020 08:34 PM

40 plus years of taking NSAIDs and pain pills .plus don’t know if we will pay for katamine plus I have to go the st-Paul Minnesota not a good time to be there with Cov and the other crap that going down.

annabanana123 06-03-2020 09:09 AM

Gotcha! Yeah my insurance refuses to pay for it so it's not an option for me right now. I can't justify spending that much money on something that might temporarily work. It's a horrible time to do that, I agree, but most hospitals are being super careful with how they handle covid versus non-covid patients. I have been to my PM and felt safe while there.


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