CFS Post-Exertional Malaise CLOSE UP
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- Опубликовано: 20 окт 2024
- Here’s what the post-exertional malaise portion of Chronic Fatigue Syndrome looks like. Few people ever see this side of the illness.
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I have a RUclips name, Truthification Chronicles, but my plans for the channel will require better equipment than I currently have and more energy than I have available at the time. Maybe in the future. The name comes from a series of novels I'm working on (they're Christian conspiracy thrillers), so I have a few conspiracy-oriented playlists of videos I discovered while doing research for the novels.
Feel better, you can do it.
I have AFib, the kind where you faint and for me I use a wheelchair. When I shop I will grab a cart and get in some exercise to keep my legs going. My spouse will sit in the chair and follow me around occasionally sitting down to rest.
Sounds like you need to take a rest. Pair a goala (peregola). Take care Deb. Your immune system is fighting your good system causing fatigue. I take a lot of meds to keep me alive and quit listening to what other people take to feel better. When you understand and accept the fact your body is fighting you and doctors are just TRYING meds to fix you. Rest, rest, rest!
Thanks for sharing the experience of CFS ...there are so many people out there with CFS and they're out of the loop so people don't know what they're going through, that sense of frustration and isolation. Faith helps so much.
Big Hugs!
Oh Deb, it pains me to see you so tired out. I understand what it is like to not be able to do what you want to when you want to do it. With my broken back, I can not plan on doing anything because there are days I can not walk and others when I feel good. I never know until that day and that moment how I will feel. I pray you feel better soon. My mother always use to say "God will never give you more than you can handle". I have lived day by day with that thought since I was only 11. I guess I'm lucky that my first accident was when I was so young, I don't know remember what a pain free day feels like. Blessings and best wishes to you!
I knew there was a reason I was drawn to you, you are my best friend from where I'm from. I never knew why she was like that, but now I know. Feel better hun
She used to love hiking too
Appreciate you so much my cfs sister
I would say "get better", but that doesn't feel right. I had major back surgery but I've had nerve damage, Pain, meds and brain fog....listening to you sounds like my life. I have some good days, but they are fewer and fewer.
So fight everyday to live life.
Daniel I'm so sorry to hear about your back. I know what you are going through, I broke my back for the first time when I was only 11. I got it fixed when I was 13 and have had it fussed from the back and from the front now. They could not put the rods in me because the screws kept shattering my bones. I have managed to break my back 3 times in the same place and in 4 other places. My heart goes out to you, I do know your pain. I would like to say it will get better, but after almost 50 years, it just doesn't. Sending blessings your way
I avoid McDonald's. I have severe me/cfs and need every molecule of real foods otherwise I bloat, fibromyalgia flares etc etc. I miss taking naps.