meawareness chronicillness chronicfatiguesyndrome myalgicencephalomyelitis chronicpain spoonie chronicfatigue mecfs millionsmissing fibromyalgia anxiety cfsme invisibleillness spoonielife fibromyalgiaawareness invisibleillnessawareness chronicillnesswarrior butyoudontlooksick chronicillnessawareness exhausted mentalhealth pwme canyouseemenow chronicpainawareness invisibledisability lymedisease lymediseaseawareness lymewarrior meaction
This thought goes through my head most days what even is a "normal" day anymore?! ♀️
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#cfswarrior #cfsawareness #chronicillness #chronicfatiguesyndrome #meawareness #myalgicencephalomyelitisawareness #myalgicencephalomyelitis #spoonie #spoony #spoontheory #CanYouSeeMeNow #invisibleillness #cfs #spoonielife #spoonylife #MillionsMissing #butyoudontlooksick #thyroidproblems
#chronicillness #chronicillnesswarrior
#lymedisease #lymediseaseawareness #lymewarrior #selflove #selfcompassion #me #meawareness
#chronicfatigue #chronicfatiguesyndrome #chronicfatiguesyndromeawareness #chronicfatigueawareness #chronicpain #invisibleillness #invisibleillnessawareness #invisiblepain #lymedisease #lymediseaseawareness #lymewarrior #cfs #chronicillnessawareness #chronicpainawareness #autoimmunediseasewarrior #autoimmunedisorder
Those were the days..
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#cfswarrior #cfsawareness #chronicillness #chronicfatiguesyndrome #meawareness #myalgicencephalomyelitisawareness #myalgicencephalomyelitis #spoonie #spoony #spoontheory #CanYouSeeMeNow #invisibleillness #cfs #spoonielife #spoonylife #MillionsMissing #butyoudontlooksick #thyroidproblems #hypothyroidism
Well that’s accurate ♀️
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#chronicillnesscommunity #meawareness #MyalgicE #mecfs #meadvocacy #cfsme #cfs #fibro #fibromyalgia #chronicfatigue #chronicpain #chronicillness #chronicillnesslife #chronicillnesssupport #chronicillnessquotes #chronicillnessblogger #chronicillnesswarrior #spooniehumour #myillnessmythoughts #butyoudontlooksick #Invisibleillness #arthrits #autoimmunedisease #spoonie #spoonies #spooniesupport #pots
Reposted from @shehaswhatofficial
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So relevant today! Sometimes you can have the most positive attitude, hard work ethic and the best intentions and your illness will still beat you!
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Hopefully tomorrow will be a better day .
#cfswarrior #cfsawareness #chronicillness #chronicfatiguesyndrome #meawareness #myalgicencephalomyelitisawareness #myalgicencephalomyelitis #spoonie #spoony #spoontheory #CanYouSeeMeNow #invisibleillness #cfs #spoonielife #spoonylife #brainfog #chronicpainwarrior #chronicpain
#chronicillness #chronicillnesswarrior
#lymedisease #lymediseaseawareness #lymewarrior #selflove #selfcompassion #me #meawareness
#chronicfatigue #chronicfatiguesyndrome #chronicfatiguesyndromeawareness #chronicfatigueawareness #chronicpain #invisibleillness #invisibleillnessawareness #invisiblepain #lymedisease #lymediseaseawareness #lymewarrior #cfs #chronicillnessawareness #chronicpainawareness #autoimmunediseasewarrior #autoimmunedisorder
|This is me. I have M.E.|
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I have M.E.
Myalgic Encephalomyelitis.
Chronic Fatigue Syndrome.
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My mitochondria do not produce the normal amount of ATP (energy). They produce less. My cells are depleted of energy and consequently my body functions at a lower level with less efficiency and a greater cost.
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Think about that for a moment.
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Everything that I do costs me more energy than the average person. I produce less energy to begin with, so everything I do is much harder, more taxing on my body and takes me longer to complete. My body has to work harder to produce enough energy to complete the task and it’s often to a lower standard because I’m so exhausted by that point.
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As a result, afterwards I am so depleted of energy, I’ve used up any reserves I might have had and dipped into future stores too, so I experience a thing called Post Exertional Malaise. A payback on my body. The true cost of spending energy. My body shuts down and I lose function, I can barely speak, think, move. I must lie in bed resting and recovering. A blank screen but behind that the systems are firing and doing their best to restore the energy reserves and top up my cells to their half filled fuel levels again; ready for me to try and pretend to be a normal human once again.
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I have M.E.
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I look completely fine and healthy in this picture I’m sharing tonight but the reality is that makeup is hiding the visible signs of my illness and the majority of my symptoms are invisible to the unassuming eye. To those who don’t know about my health, they will not see any illness. It’s only those who are familiar with me and the signs I typically present with, who can see my illness.
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This week is M.E Awareness Week.
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Every year it comes around and every year I say to myself I’ll be more on it next year and do my best to play a larger part in raising awareness but the thing is, every year my M.E has gotten more severe and I really don’t have the spare energy to write a lot of posts and be super proactive in raising awareness.
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{continued in comments}
Collecter les statistiques #MEAWARENESS effectuez une recherche à l'obtention des statistiques (Aller à la sélection).