I wanted to create this page as a way to bring people with CFS/ME together; build a network of friends and raise awareness.
England, United Kingdom
Joined October 2018
- Tweets54
- Following31
- Followers33
- Likes62
CFS/ME Friends retweeted
Anyone struggling with coughs, colds and infections at the moment?!
You need these 👇🏻 in your life !
Stronger immune system to keep those coughs and colds at bay!
Capsule packages… instagram.com/p/Bqo6EyPlOci/… – at Ilford, London
Sunday Dont let it be a day of anxiety enjoy the day and do the little things that make you happy run a bath listen to music, doodle watch a movie let mondays worries be for monday x #SundayThoughts
CFS/ME Friends retweeted
Please don’t judge people. You don’t know what it took someone to get out of bed, look and feel as presentable as possible and face the day. You never truly know the daily struggles of others. ~ Karen Salmansohn
here is a link to all different support services for ME/CFS in different regions
meassociation.org.uk/informa…
Love this #November #NovemberWish
As we head into #November and the nights draw in & the weather gets colder, I’d love to hear any #joyinautumn moments you may have! I’ll retweet any I come across with the hashtag #joyinautumn! ☺️🍁🍂☕️🧡
Read more here!
notjusttired.com/2018/10/08/…
Are super power should be never be invisibility, raise awarness for the very real visible people suffering from invisible illnesses #ChronicPain #Chronicillness #invisibleillness #me #CFS #cfsme
Its so hard when the clocks go back and winter strikes, the air in your rooms deadly cold and putting clothes feels discusting. Having a shower and dreading stepping out only to feel your wet hair turn to -10 as you cling to the hairdryer blowing your body as you blow your hair
These are lovely xx
These jasper charm bracelets are a beautiful way to show your support/understanding to a warrior friend or relative, or a well-deserved pick-me-up to brighten your day! Link in bio 😊 #ChronicWarriors #EhlersDanlosSyndrome #Zebra #chronicpain #warrior #chronicillness #spoonie
CFS/ME Friends retweeted
“If you love someone with an invisible illness, a little understanding is the kindest offering you can make.” Living with Disbelief of #InvisibleIllness and Pain buff.ly/2E48Tpv #chronicpain #disability #chronicillness
I wrote this post on the service provided by Manchester airport for #invisibledisabilities. I had no idea it existed until recently & so I wanted to share my experience in case it helped someone else as it did me. #InvisibleDisabilitiesWeek #pwME #spoonie
notjusttired.com/2018/10/17/…
CFS/ME Friends retweeted
When I collected my son from nursery yesterday, I had to fill in a form. Brain fog was making this challenging & I ended up telling my son’s key worker that I have #mecfs. She had no idea! Said it shows how we don’t know what others are dealing with #InvisibleDisabilitiesWeek 1/2
your problems still affect your wellbeing and happiness and you shouldn't feel bad about talking about them x
