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Anyone with LC 4 years

Post-COVID Recovery & COVID-19 | Last Active: Feb 17 4:30pm | Replies (55)

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@dac777

I didn’t know there was a name for it. I know what you mean. I haven’t sought out any answers because I don’t feel anyone takes me serious or is willing to try to figure it out. It takes more energy to try and go to the doctors then just to try and deal with it. My nervous system definitely hasn’t been the same since Covid. I had it at the end of November 2020. That was no ordinary virus. They will NEVER convince me otherwise.

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Replies to "I didn’t know there was a name for it. I know what you mean. I haven’t..."

I have found all my doctors tire of me when they can’t help. Some are not actually dismissive, but they don’t have anything that actually helps me. I’m sure it is frustrating for them too.

I still go to a few appointments, but less as time goes on. I am three years into this and have been to hundreds (yes hundreds) of appointments.

No, this is no ordinary virus.

I have sought answers - and relief - running myself ragged to do so, to no avail. I w tried just about everything. I find it so hard to accept that I have to accept this as my reality for the rest of my life. 😢