Anyone think that it’s no longer long Covid? just permanent damage?

How did you get BC007?
Are you in USA?

I certainly hope that COVID long haulers is not permanent. I can no longer walk without the aid of a cane and even then I can’t go very far without wanting to fall down. MY balance is shot and I am hoping a solution will be found. I have been like this for almost 3 years now.

I’m in the US. As far as I know no drug trials are taking place in the US with BC007. The only ones I’ve read about are the trials in France.

Yes... we need a reputable, reliable data base in order to navigate all these potential alternative treatments! I am hoping the Covid specialist will shed some light on this when I finally get to see him next month.

Me too. Only they have diagnosed me with Parkinson's and I fear it will only continue to get worse now. I don't think the experts know much. And no one seems to be willing to even entertain the idea that this was created in a lab and meant to be a super virus. Maybe it was not meant to be released. But it sure has wreaked havoc on so many of us.

Living the exact nightmare

you are not alone, the memory, brain fog or what ever the heck it is as well as a whole other mess of things is what i'm going through too, it's been over 3 years for me, i have to take it day by day..hang in there..

What have you tried and what kinds of doctors have you seen? I went to my GP, a neurologist recognized in the area, eye doctor, and now soon a couple ENT’s. So far no idea what to do except therapy, which I have done repeatedly with no help. I am looking for some fresh ideas.

So sorry, I can relate. I hope you can find a way through this. I lost my career, marriage and many people along the way. But I’m trying to find acceptance and selfcare practice.

I’m my case l know is permanent damage. The MRI, Encephalogram and Evoke test showed abnormal function of the left temporal lobe and frontal lobe. The test results are compatible with my symptoms l never had before. Brain fog, slight short term memory, insomnia and right hand tremor. This retired me from practicing orthodontics. There are no drugs to fix brain damage. At least l can function for daily life, although l battle with the tiredness of the inability to sleep and rest. I still exercise, eat right, take supplements and push my self. The Ambien is the only consistent med l take now, but is hit or miss. Accepting the situation has allowed me to get off anti depressants. Until stem cell research and usage for treatment, l don’t see pharma curing anything. That won’t happen in my lifetime.