When to accept permanent long covid?

Please, first and foremost we must always remember to support one another. The people here are wonderful about doing that. Best wishes and good luck to everyone.

I’m 3 years+ long covid and still experiencing the same neurological symptoms I developed after my first covid infection in 2/22. I’ve since had three more, none of which could be described as mild, in 3/23, 2/24, 3/25.
My symptoms of head vibrations, rumbling and feeling ‘full’ never go away, but headaches are better. Diffuse body pain is awful, especially in the early morning hours before daybreak, and this is a more recent symptom.Fatigue comes and goes, often with no prior physical exertion. I have fallen asleep out to dinner with friends several times. Could not keep my eyes open. I have accepted that I will have these symptoms for the rest of my life- and maybe in the one beyond as well! But I do hope those of you reading this will be lucky, and your symptoms will eventually abate. Good luck, all.

I can relate to morning and evening body pain, regardless of exercise or no exercise.
I have ongoing fatigue, but not all the time. I do sleep a lot, and honor the fact that I am tired. I don't fight it.
My symptoms rotate, and include brain fog, balance, and an annoying wet cough that's been treated and examined. Still there, but not as prevalent.
This has shifted my lifestyle, 2 years now, and I'm going with the flow of it all. I'm 78 and not giving up...things are just different.
I wish you well.

I can relate to morning and evening body pain, regardless of exercise or no exercise.
I have ongoing fatigue, but not all the time. I do sleep a lot, and honor the fact that I am tired. I don't fight it.
My symptoms rotate, and include brain fog, balance, and an annoying wet cough that's been treated and examined. Still there, but not as prevalent.
This has shifted my lifestyle, 2 years now, and I'm going with the flow of it all. I'm 78 and not giving up...things are just different.
I wish you well.

You are absolutely correct....the people on this site are positively, absolutely, definitely wonderful in every way. I spent five years not knowing any LC survivor and then found the Mayo site. It is beyond heartening to finally learn that many people understand and are willing to "listen" to what the rest of the world seems to have forgotten or at least pushed aside. Being able to read postings at any time is uplifting because it is like having friends available 24/7. I chose not to enroll in a local world-renowned hospital's LC "clinic" after learning it was only a data collection center in order to prepare for the next epidemic. To get to that location required feeling well enough to drive through heavy city traffic, locate difficult parking and walk a long distance to reach the clinic...not for this breathless, arthritic 79 year old cancer patient on a cane. I've not heard of any medical facility actually "curing" LC while some individual doctors may offer more improvement than others via trial and error or sheer luck. We have such a wide range of symptoms, even though some symptoms are universal, that we ALL are our own best hope, best source of information and the most understanding of one another's plight. Physically we may never be the same as pre-Covid. However, we have one another to lean on, learn from, feel appreciated by and be heard. For all those reasons, we are a very special group of caring individuals who uplift one another. Sometimes it comes down to one human caring about another human...that's US!!! Only those who have LC understand others who have LC. Learning from this site and hugging you all lifts spirits!

I am looking for someone who has Long Covid issues their mouth & sinuses. It h as been over 2 years. I have had 16 doctors. How can I find SOMEONE WITH MY SAME PROBLEM???

I can relate to morning and evening body pain, regardless of exercise or no exercise.
I have ongoing fatigue, but not all the time. I do sleep a lot, and honor the fact that I am tired. I don't fight it.
My symptoms rotate, and include brain fog, balance, and an annoying wet cough that's been treated and examined. Still there, but not as prevalent.
This has shifted my lifestyle, 2 years now, and I'm going with the flow of it all. I'm 78 and not giving up...things are just different.
I wish you well.

What are your mouth issues? My brother who I believe has long covid say everything tastes different or he can’t taste a lot of things. No sinus issues.

My mouth is constantly full of Thick sticky mucus!

What are your mouth issues? My brother who I believe has long covid say everything tastes different or he can’t taste a lot of things. No sinus issues.