Anomalia temperatury powietrza. Prognoza na Listopad 2022 z dnia 2️⃣0️⃣.1️⃣0️⃣.2️⃣0️⃣2️⃣2️⃣
model #CFS/#NCEP #Meteomodel
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The Royal Horticultural Society is the UK's leading gardening charity; inspiring everyone to grow. #AutumnGardenDays
Wise words from Michael J. Fox
#chronicillness #Parkinson #MS #ME #CFS #Fibromyalgia #LongCovid #postviraldiseases #Lyme
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I spoke at Rally yesterday on behalf of those people with #ME and #CFS unable to come, and to demand more info and training for drs, more research & benefit changes.
Ruth is one of the ME missing who couldn’t come. #helloRuth
#MillionsMissing
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farm postin' update number 26 that's an integer!
low energy day thanks to #cfs but I got there and did some woodwork for the infrastructure projects and a few other bits- lots of mushrooms, air smells rich and earthy and the leaves are turning :)
Stay safe, stay fabulous
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MECFS + Long Covid patients: undercounted, neglected medically, socially and financially.
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“When faced with a new complex disease and a lot of unknowns, [medical professionals’] default is to psychologize it, gaslight it, attribute it to something else.”
theguardian.com/society/2022/o
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Your #donations make sure Simcoe Muskoka residents can get help right away, without waiting for an appointment with their doctor or using the emergency room for non-urgent care. Your donations ensure we can help those who have nowhere else to turn. #cfs cfssc.ca/donate/
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Thoughts & Solidarity ✊🏻 ❤️🩹 to all in person & online heading to parliament square today
#WeAreAllConnected #MillionsMissing
#MEcfs #CFS #MyalgicE #PwME
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For many with #POTS and #CFS/ME, it is important to pace yourself and stay within your "energy envelope" so that you don't trigger a flare. What fits in your energy envelope? Check this page to help you think about pacing. standinguptopots.org/livingwithpots
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curious what others are doing for #fibromyalgia/#cfs-related stiffness if anything?
sometimes, i feel like tin man—all rusted out.
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New #tag #energyimpaired for whatever reason inc #ME #CFS should be a recognised disability #InvisibleDisabilitiesWeek
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The #CFS Diagnosis was solitary confinement in prison for 28 yrs!
My Cardiologist gave me the keys to those prison doors with the proper Diagnosis of #Dysautonomia and set me free!
Celebrating 4 yrs of successful treatment during #DysautonomiaAwarnessMonth!
#makenoise4turquoise
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big #fibromyalgia/#CFS teaching:
i had a flare and literally rested all weekend for the first time in months.
it didn’t help my pain/fatigue at all—i honestly feel better when i just push through even if sometimes, that’s easier said than done.
stay active, my friends. 💪🏻
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