THANK YOU ALL. They say that it is hard to say sorry and similar to say thank you, when you REALLY mean it. I wish nobody suffered from this horrible debilitating illness but I feel such love and sympathy knowing that I am not alone and it's not all in my mind. BIG LOVE to all who feel this pain and enjoy the moments when the pain is minimal or we are so happy doing something we enjoy that makes the pain secondary. Life is precious and so are YOU whoever reads this BIG WARM HUGS and make the most of your life.... Oh SH*T I have left the iron on... (Just kidding life is too short to iron clothes...dry them properly and the creases are almost impossible to find) X
This always seems like a strange thin... - Fibromyalgia Acti...
This always seems like a strange thing to say....
Thank you! Big love to you too and I agree about ironing👍If I learned anything over the tumultuous past 2 years, it is that life is indeed precious. What a lovely post to start my day with😊
Awwww thank you very much, love and hugs sent your way. It means a lot to us all 💕🌈💕
Thank you - and i agree 100%... Life is definitely too short to do ironing 😉😉😉
Ironing! what’s that lol 👎
Gentle hugs back to u. We all know what every person in here has to endure and that people who live with chronic pain are the strongest on the planet. We carry on fighting when most give up with slight acute pain. Go us! Don't need to iron if you go clothes free lol! 🤭🤣
This made me cry because of the empathy. First time I've tried a support group for this horrid condition (recent diagnosis) and it's amazing for me to find people with the same thing, going through the same things. 💓
That's beautiful. Thank you for taking the time to post that 💓
Hi Chris,
Your right, if I think of all the problems I’ve got at the moment it’s enough to drown my sorrows, fibromyalgia and CFS, anxiety and panic attacks and depression, oseopenia which is the start of thinning of the bones stage before osteoporosis, Barrett’s disease and having biopsies taken of my osoephagus on my birthday with only a sedative because they are short of anaesthetists, bowel problems, neurological overload which was like a stroke and neurologist said it would take 6-12 months to go back to normal as my brain was running on empty, I used to go to the gym but now it’s proven that exercise isn’t good for people with fibromyalgia/M.E./CFS so not all the muscle definitions have gone out of my arms and legs, I’m only 56 this year and it’s the first time I actual feel my age, any suggestions to get my mojo back please 😔