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Dose anyone else feel like neuropathy is taking over their life?

Neuropathy | Last Active: May 29 12:22pm | Replies (97)
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@johnbishop

Hi Linda @lindaww, I see that you joined Connect in 2020 but today is the first time you have posted so I would like to welcome you to Connect. Sorry to hear that neuropathy has been taking over your life. It can be the pits trying to find some sort of relief or something that helps on a daily basis. Not sure if you have seen the Foundation for Peripheral Neuropathy site but they have a lot of helpful information - https://www.foundationforpn.org/living-well/.

There are also a lot of different discussions on Connect for what helps neuropathy. Here's a link that shows all of the different discussions if you want to scan through them to see if there are any that might help - https://connect.mayoclinic.org/search/discussions/?search=neuropathy%20what%20helps

Are you able to share a little more about your neuropathy diagnosis?

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Replies to "Hi Linda @lindaww, I see that you joined Connect in 2020 but today is the first..."
lindaww | @lindaww | May 29 12:22pm

I have critical illness neuropathy. in 2020 as covid first started, i had influenza A, sepsis and pneumonia . I was the only person in fargo on a ventilator that did not have covid. 47 days later I started waking up. i thought i was in hell, as it was dark, and all i saw was what looked to me like something ready for sacrifice. The next time i woke up, it was daytime, and i realized that what i thought was sacrifices was people laying under white sheets. So of course I thought I was in a morgue. more to story but cant put it down right now. I still cry when i realize what happened to me

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