Long Covid symptoms

Posted by denny58 @denny58, Nov 1 6:14pm

Any suggestions for managing symptoms of Long Covid or possible CFS chronic fatigue syndrome?
I am 67 year old female. Prior to having positive Covid last Christmas I occasionally experienced Chronic fatigue symptoms. Since Covid symptoms have worsened where I have extreme weakness, fatigue, body aches and am unable to get out of bed all day, like today. I also experience shortness of breath or inability to take a cleansing breath. I am also affected by sensory issues of noise and light, preferring shades drawn and quiet which is difficult at times when the train goes by near our home despite living in the country or our dog barking.
Thankfully I’m retired but nonetheless find it frustrating when I’m not able to get out of bed and take care of household chores or attend social events. Husband is somewhat supportive but not completely understanding when I have days like this, 1-2+ times/week.

Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.

When you say you occasionally experienced Chronic fatigue symptoms, how long did these bouts last, how long ago did they start, and approximately how many times did they occur?

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Profile picture for Colleen Young, Connect Director @colleenyoung

@suefish, glad you're back on with your new phone. If you have any technical issues, you can contact the team using this form https://connect.mayoclinic.org/help-center/

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@colleenyoung @suefish thanks to you all for helping me get back to the “party.” Tough starting with new phone. ❤️

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Profile picture for suefish @suefish

@suefish am I making progress in rejoining “the group.”

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@suefish help to all of you.

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Profile picture for sanDGuy @sandguy

When you say you occasionally experienced Chronic fatigue symptoms, how long did these bouts last, how long ago did they start, and approximately how many times did they occur?

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(This is directed at Denny58, to the initial post of this subject/thread)

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Profile picture for robinrm @robinrm

@lkirnbauer thank you for that information. Everyone I talk to discourages me for doing this. My daughter wants me to do the nicotine patches. Have you ever tried those and if so, did you get any relief or adverse effects? You’re lucky that your insurance paid for this I don’t believe mine will pay for it. It seems to be hit and miss if they work for people. Some people say they work the first time and then the second time they didn’t work at all, but I guess unless I try it, I won’t know. wishing you the best as well.

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@robinrm Why are they discouraging you to get the SGB? Don’t they want you to feel better? I have not tried the Nicotine Patch as I am a former smoker and don’t want to get hooked again. They will be my next step however. I am currently having Green Violet Laser Light Therapy at my Chiropractor’s office in the Chicago area in Geneva, Il and have gotten a tiny bit of smell back on occasion. I also hadn’t tasted any flavors in 3 years as I have no taste or smell and I tasted the flavor of lemon from a sucker I was eating, just a quick taste and then it was gone. I haven’t had that sensation in a very long time, so this treatment is promising to me. What the SGB did for me was really help my PTSD/Anxiety. If you can afford to have them, do it and post your experience here. Good luck!

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