Full version here: • ME/CFS: 5 early mistak... "M.E./CFS Mistakes I made early on" Was originally posted a few years ago. This is the shortened version.
I still over accomodate and push through; learning something every single day! And I definitely focus on what I can do now, and not what I’m no longer able to do. Since being diagnosed in 2018, when I knew literally nothing about CFS, I could now probably take a Masters 😂 Thanks for your channel from the UK x
I usually am thankful for what I can do when I can, but I have gotten discouraged at times when some tasks that were easier for me to do before can be difficult. Thanks for the video.
Great video😊Just to be animated especially with littlies nearly kills me😢Try to be positive but hard when unable do anything or see anyone💔😢yep short versions are great when its all your capable of= me today.Want to watch long vers.asap.Hi from Australia & yep been sharing👍🏻😊
🎉BRILLIANT! ME/CFS since early 1960s Covid-19 & LH Covid since 2020 I'm just now learning to adjust. Haven't figured it all out yet. Gaslit by Doctors for decades. The medical community (Especially Doctors & Staff who've had Covid) is slowly coming around! Stay positive EVERYONE!
I can arrest to the fact that pacing when in the Philippines is impossible. Invisible illnesses just don't exist here. Expectations if family involvement are very high. As such, I'm now very poorly indeed. My IBS has gone crazy, I'm exhausted to non functioning much of the time. I'm so thankful to be heading back to the UK tomorrow. Many flying hours where sleeping will be my only objective. I've fallen out with family here who just disregard my ME. to the point I found myself driving in a very dangerous state, indeed, driving off the road three times. I'm not seriously considering whether or not I should come back again.
How do you find an ME literate doctor? I've been through so many doctors over the years and none have helped me. None have ever even heard of ME. I'm starting to think I'm the only person in New Mexico who has this. I've seen 20+ doctors in four years, and not a single one has ever seen another patient with ME.
Full Version of video here: ruclips.net/video/YMYOZoi22J8/видео.html
Look fwd to it😊
I still over accomodate and push through; learning something every single day! And I definitely focus on what I can do now, and not what I’m no longer able to do. Since being diagnosed in 2018, when I knew literally nothing about CFS, I could now probably take a Masters 😂 Thanks for your channel from the UK x
I usually am thankful for what I can do when I can, but I have gotten discouraged at times when some tasks that were easier for me to do before can be difficult. Thanks for the video.
These short versions are super convenient. Thank you!
Thanks, good advice…difficult to focus on what I can do now, not what I used to do.
Great video😊Just to be animated especially with littlies nearly kills me😢Try to be positive but hard when unable do anything or see anyone💔😢yep short versions are great when its all your capable of= me today.Want to watch long vers.asap.Hi from Australia & yep been sharing👍🏻😊
Great info and I appreciate the more accessible shortened version :)
🎉BRILLIANT!
ME/CFS since early 1960s
Covid-19 & LH Covid since 2020
I'm just now learning to adjust. Haven't figured it all out yet.
Gaslit by Doctors for decades.
The medical community (Especially Doctors & Staff who've had Covid) is slowly coming around!
Stay positive EVERYONE!
Thank you 🙏🏼
Thank you so much ❣️
Thank for this ❤
🥀thank you so much🥀
I can arrest to the fact that pacing when in the Philippines is impossible. Invisible illnesses just don't exist here. Expectations if family involvement are very high. As such, I'm now very poorly indeed. My IBS has gone crazy, I'm exhausted to non functioning much of the time.
I'm so thankful to be heading back to the UK tomorrow. Many flying hours where sleeping will be my only objective.
I've fallen out with family here who just disregard my ME. to the point I found myself driving in a very dangerous state, indeed, driving off the road three times.
I'm not seriously considering whether or not I should come back again.
How do you find an ME literate doctor? I've been through so many doctors over the years and none have helped me. None have ever even heard of ME. I'm starting to think I'm the only person in New Mexico who has this. I've seen 20+ doctors in four years, and not a single one has ever seen another patient with ME.
Thank you for these videos. Does anyway else have chest pain called Costochondritis from having ME/cfs?
I've had it, but that was before I had ME. Not fun! Sending hugs. ❤
Doctors huh pill pushers