Post Covid Symptoms and what has helped me.
I have fibromyalgia and post thyroid cancer in 2000. Got Covid May 2022. Have all of the symptoms long haulers experience. Dizziness, hair loss, canker sores in mouth, brain fog, trouble focusing, fatigue, muscle aces and pain, muscle weakness, etc, etc. Have had eye exam with a small spot behind my retina that was not there on exam before Covid. Working with PT doing the same exercises others have explained. Seems that Covid has increased my fibromyalgia symptoms. Working with my primary doctor with treatment. I have started low dose naltraxone and this helps with brain fog, decreasing the pain and helps with sleep. Along with the PT I hope this is going to help in the long haul. I also take an antihistamine for my ears and head stuffiness, thyroid replacement, celexa for anxiety and calcium with vitamin D. Hoping to be on the mend soon. Hope this may help anyone else dealing with this too
Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.
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I occasionally have a smell of something that is burnt or scorched. As for my gabapentin I'm prescribed 800 mg 3x per day . And I have noticed more aches and pains in my joints but I chalked it up to getting older lol... I'm 50. But I do have some deep bone pains from time to time .. it's not muscle or joints, it's the bone itself. When I was sick with covid my legs especially my upper thighs hurt so very bad and that's happened to me about 4x since I got better. But it's almost debilitating.
And you're right , this forum is like therapy because it's good to know we're not alone and it's not all in our head. It's very real and there's still so much that's not known about it. Another bit of info I have NOT taken the Covid vaccine and I absolutely refuse to. I understand that everyone have their own reasons for taking it and that's perfectly fine. I'm just saying it's not for me .
Thanks to all who have commented as I feel it helps us all. Oh and another thing about my neuropathy I have a spot on my back about the size of my hand that is completely numb but sometimes it will itch and burn so bad and it does no good whatsoever to scratch it because I can't feel it.
Anyway thanks for listening to my rambling and I appreciate others comments more than you know!!!
Thank you for all you're helpful advice! I wish you much more success! May God bless us all!
I could give a lecture in HRV and you symptom recovery.
HRV lectures
https://open.spotify.com/episode/1FbttJqosfnIOZNqLbK8zm?si=kffziEVSTc-IvncGvOfVUw
https://open.spotify.com/episode/49jIF8k8x9HIF0ua5VPRGM?si=a6rKqMOPRC-7zjhcly3B0g
https://open.spotify.com/episode/0RfMjnPxPLdGhgRzdDgufX?si=-KezYqLmSqOPGoYc8AbYEA
https://open.spotify.com/episode/7plGDhXWCJzfEXeB1YE1aP?si=RnlmtItzSiu3c3PnFYQeQg
https://open.spotify.com/episode/4IhCHbXWlOKQr5Ey3WGZXa?si=kpxbnaVmRQCSAM5TmZyKNw
If you have questions or need help. I have a few rules.
Due to the neurological nature of my recovery. I can experience a relapse in symptoms. I allow people to describe their symptoms one time and after that insist you refer to them as symptoms.
I am a retired Bonemarrow Transplant Nurse. I’m an advocate for myself and other. The best way I can help you is to teach you how to advocate for yourself and the roles health care providers play, coverage insurance companies can provide. More importantly how you can take back your life.
All I ask is you give me the feedback of how my advice has helped. We are all in this together.
You are the biggest influence on your recovery. The healthcare system is learning as we are. Have a hopeful outlook. Remember what you knew before you were struggling.
Even though COVID is the first pandemic of our age. There are many know. Modalities to treat yourself and recover.
My husband has long covid. He has experienced many dental issues post covid. He has had root canals and had to remove teeth that got abscesses after covid. Any others experienced this?
Your symptoms were so well stated. You will never know how reassuring it is to know that others are experiencing these conditions. At the time of the initial “itch” I developed a very light brown area about the size of my hand (upper left shoulder blade). So interesting that we have had some of the same conditions, including the smell of metal.
Finally I visited an immediate care.
The “itch pain” was so uncomfortable, weeks later went to the NWMH ER immediate care in Chicago at 8:00am on a Sunday.
The ER DR. checked me for shingles which had negative
results. I understand her visual observations and TRYING to understand what it could be for her patient. Her photographs of my itch area did not capture the brownish spot. 🙁 only the small scratch marks.
Thank God, for my neurologist and my prescriptions.
Will this itch continue and be a permanent condition?
Truly, at this time, I do not think there is an answer.
Strength and prayers.