This is My Life…. VJHealth, ME/CFSHealth, ME/CFS, Myalgic Encephalomyalitis21 Comments Share this: Share on X (Opens in new window) X Share on Facebook (Opens in new window) Facebook Email a link to a friend (Opens in new window) Email More Share on Pinterest (Opens in new window) Pinterest Share on Tumblr (Opens in new window) Tumblr Print (Opens in new window) Print Share on LinkedIn (Opens in new window) LinkedIn Share on Reddit (Opens in new window) Reddit Like Loading... Related
For those who are experiencing Long Covid can relate to ME/CFS, sharing many of the same symptoms. Thanks for sharing. LikeLiked by 1 person Reply
Yes, and actually, since Covid I’ve had more medical empathy. Doctors will say this looks like Long Covid. I don’t bother to tell them I’ve had it since long before – just glad they are paying attention. LikeLiked by 1 person Reply
I’m looking into getting a health maintenance band to help with conversing energy since I’ve had Covid. I feel like I have less stamina. LikeLiked by 1 person
Thank you for posting this, VJ. It’s a very well done! I sharing your post to my FB and my X page to help educate others. LikeLiked by 1 person Reply
Thank you for sharing this, VJ. It gives us a better undertanding of MECFS. LikeLiked by 1 person Reply
Wow – what a great analogy. The whole idea of battery level and apps running in the background makes so much sense. Thank you for the education, VJ! LikeLiked by 2 people Reply
Thanks, VJ, I know much more about ME/CFS now. Great video on the subject. LikeLiked by 1 person Reply
Thank you for sharing this video, VJ. It does an excellent job to explain MECFS and thus create awareness and understanding. LikeLiked by 1 person Reply
I thought so. I know people, including my family, struggle to understand. Thanks LikeLiked by 1 person Reply
One Woman's Quest II 
For those who are experiencing Long Covid can relate to ME/CFS, sharing many of the same symptoms. Thanks for sharing.
LikeLiked by 1 person
Yes, and actually, since Covid I’ve had more medical empathy. Doctors will say this looks like Long Covid. I don’t bother to tell them I’ve had it since long before – just glad they are paying attention.
LikeLiked by 1 person
I’m looking into getting a health maintenance band to help with conversing energy since I’ve had Covid. I feel like I have less stamina.
LikeLiked by 1 person
It’s real. I hope you find a way to manage it. 🤗
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It’s definitely real! Thank you, me too! ❤
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Thank you for posting this, VJ. It’s a very well done! I sharing your post to my FB and my X page to help educate others.
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Thanks so much Susan.
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Thank you for sharing this, VJ. It gives us a better undertanding of MECFS.
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That is the hope, thanks Eugi
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You’re welcome, VJ.
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Thank you for posting this clear, informative video.
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Appreciate you taking time to watch, Liz.
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Wow – what a great analogy. The whole idea of battery level and apps running in the background makes so much sense. Thank you for the education, VJ!
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Thanks Wynne. It helped me too, lol.
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Thanks for sharing this video VJ. It helps us understand MECFS.
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Appreciate that you took the time to watch.
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🙏🏼🙏🏼🙏🏼
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Thanks, VJ, I know much more about ME/CFS now. Great video on the subject.
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Thanks Lou, for watching.
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Thank you for sharing this video, VJ. It does an excellent job to explain MECFS and thus create awareness and understanding.
LikeLiked by 1 person
I thought so. I know people, including my family, struggle to understand. Thanks
LikeLiked by 1 person