#High5ME for taking off the nail varnish on my toes and mega quickly painting my nails before bed. Little things that are exhausting but mentally make you feel better. #ME#lifewithanewborn
Caring for a son with #MECFS@ALLIANCEScot
“Do they think it’s all in my head, Mum?” my son quietly asked as we left the GP surgery.
“I can assure you, son, none of this is ‘in your head’” I replied with conviction. He was 20 & had been diagnosed w/ M.E.
https://t.co/aM976CzHNs
"Imagine your worst hangover combined with the flu permanently".
ITV Channel reporter @GaryBurgessCI opens up about his ME diagnosis, which forced him to take a step back...
“The truth is, we never really feel well. I honestly don’t actually remember what it’s like to feel 100% well anymore, it’s been that long” by @mcfindoone
#mecfs#pwME#MEAwareness#chronicillness#spoonies
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“But people don’t see us on our bad days – they don’t see us when we crash. ME has two faces – the one people see, and the one which is hidden from the outside world because we are too ill to be seen” by @JourneyFog#pwME#MEAwarenessMonth#mecfs#spoonie
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@High5_ME Omg you had a baby?! Wow congratulations! I sometimes find awareness day scary because my brain thinks we’re all irretrievably screwed, and then you go and grow a HUMAN and it’s such a blessing and reminder that maybe blessings can come, with this illness xx
I missed #MEawarenessday because I was welcoming this new member into our family. A magical #High5MEmoment for being able to grow and birth this perfect human.
Re-sharing some of my interviews with #pwME for #MEAwarenessMonth.
This one is with the lovely @High5_ME
“I find it frustrating that ME is so underestimated, the pain, exhaustion and heart breaking emotions we feel.”
#MillionsMissing#MEawarenessDay
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#mydailythankyou ~ grateful I managed to finish my latest blog for #MEawarenessweek! I certainly have to plod my way through my blogs but it’s worth it when I finally finish them! 😅
So very grateful to all the #pwME who contributed 💙 #MillionsMissing
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