Me: [Downing my 5th coffee of the day] “If your cells’ mitochondria don’t synthesise their own ATP properly, store-bought is fine.”

#autoimmune #mitochondrialdisease #chronicdisease

[Automatic repost https://twitter.com/dystobot/status/1654547796890886145]

RT @4Lilyfoundation: We're proud to support #dystoniaawarenessweek - often people diagnosed with #mitochondrialdisease are also affected by dystonia. How much do you actually know about this movement disorder?

https://t.co/eDlhrKxxhJ https://t.co/FvemRq541X

[Automatic repost https://twitter.com/dystobot/status/1653687124237905924]

RT @4Lilyfoundation: Today marks the beginning of #dystoniaawarenessweek. Did you know dystonia is one of the most common movement disorders in children with #mitochondrialdisease?

Right now #mito is incurable, but we're working hard to find a cure. Help us end the suffering: https://t.co/DNW6dKYwjD https://t.co/CxLNXoKZ4E

[Automatic repost https://twitter.com/dystobot/status/1630635229034557440]

RT @LadyFaye31: #RareDeseaseDay #LeighsSyndrome #dystonia #mitochondrialdisease alone we are rare, collectively we are stronger, together supported we are heard 💪🏽 https://t.co/zqkcnWF8CZ

https://gofund.me/9cf30242
#MitochondrialDisease is a very rare condition. Please take a wee second out your day to read about my niece and nephew. 2 of only 3 people in Ireland living with condition.
Please share and help raise awareness of not only Tommy and Grace but the condition as a whole.
Many thanks and much love.
Have a great day

RT @MitoResearch: Thank you to @ALewerMBE for joining our parliamentary event to find out more about #mitochondrialdisease & the importance of raising awareness for the benefit of the whole #mito community @4Lilyfoundation @GeneticAll_UK @UniofNewcastle @wellcometrust #projectpearl #RareAPPG

🐦🔗: https://n.respublicae.eu/ALewerMBE/status/1600547125586116608

Please consider helping my friend Josie #gofundme, #mitochondrialdisease https://gofund.me/9b524f6d
Thank you!