Tom Kindlon

Tom Kindlon

www.facebook.com/TomKindlonMECFS
Dublin, Ireland / Myalgic Encephalomyelitis patient 28 yrs. Pins on ME/Chronic Fatigue Syndrome or #ChronicIllness/#InvisibleIllness/#Spoonie. Not all pin wordings my own.
Tom Kindlon
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Tippi Helsson‏  @TippiHelsson  Nov 15 More #pwme lost in their beds. ME is a monster. #endmecfs #MillionsMissing #MyalgicE #timeforunrest

Tippi Helsson‏ @TippiHelsson Nov 15 More #pwme lost in their beds. ME is a monster. #endmecfs #MillionsMissing #MyalgicE #timeforunrest

Chronically Hopeful‏  @chronic_hopeful  21h21 hours ago More #MECFS isolates us from the life we have been living due to #sensoryintolerance to light, sounds & movement around us.  Going out & living life causes a pain & exhaustion that is hard to cope with.  We isolate ourselves to survive.  #chronicillness #ChronicPain #ChronicFatigue

Chronically Hopeful‏ @chronic_hopeful 21h21 hours ago More #MECFS isolates us from the life we have been living due to #sensoryintolerance to light, sounds & movement around us. Going out & living life causes a pain & exhaustion that is hard to cope with. We isolate ourselves to survive. #chronicillness #ChronicPain #ChronicFatigue

Chronically Hopeful‏  @chronic_hopeful  21h21 hours ago More #MECFS A common misconception is that we're just tired, but sleep doesn't take away this #exhaustion & every tiny movement makes it worse. The ironic thing is that most of us struggle to sleep despite our #fatigue. #NotJustTired  #pwme #chronicillness #ChronicFatigue #ChronicPain

Chronically Hopeful‏ @chronic_hopeful 21h21 hours ago More #MECFS A common misconception is that we're just tired, but sleep doesn't take away this #exhaustion & every tiny movement makes it worse. The ironic thing is that most of us struggle to sleep despite our #fatigue. #NotJustTired #pwme #chronicillness #ChronicFatigue #ChronicPain

10 Things Not to Say to Someone with #MECFS.  Created with input from #pwme.  Please share wildly - hopefully it can help make some difference.

10 Things Not to Say to Someone with #MECFS. Created with input from #pwme. Please share wildly - hopefully it can help make some difference.

SolveMECFSInitiative‏  @PlzSolveCFS 20h20 hours ago More Share this quote graphic, if you can relate. #SolveMECFS #MECFS

SolveMECFSInitiative‏ @PlzSolveCFS 20h20 hours ago More Share this quote graphic, if you can relate. #SolveMECFS #MECFS

Julie Duffy ‏  @JulieDuffy4 4h4 hours ago More Don’t forget to extend your kindness to yourself!   #worldkindessday #KindnessDayUK #Kindnessmatters #selfcare #KindnessToSelf

Julie Duffy ‏ @JulieDuffy4 4h4 hours ago More Don’t forget to extend your kindness to yourself! #worldkindessday #KindnessDayUK #Kindnessmatters #selfcare #KindnessToSelf

A poem by @CorinaDuyn, an artist with #MyalgicE, summing up the unfortunate payback in the illness.  From her book, Hatched, http://www.corinaduyn.com/site/buy-wellness-art-and-books-by-corina-duyn/hatched-re-hatched/ … (posted with permission)  #MEcfs #CFS #MyalgicEncephalomyelitis

A poem by @CorinaDuyn, an artist with #MyalgicE, summing up the unfortunate payback in the illness. From her book, Hatched, http://www.corinaduyn.com/site/buy-wellness-art-and-books-by-corina-duyn/hatched-re-hatched/ … (posted with permission) #MEcfs #CFS #MyalgicEncephalomyelitis

A poem by @CorinaDuyn, an artist with #MyalgicE, summing up the unfortunate payback in the illness.  From her book, Hatched, http://www.corinaduyn.com/site/buy-wellness-art-and-books-by-corina-duyn/hatched-re-hatched/ … (posted with permission)  #MEcfs #CFS #MyalgicEncephalomyelitis

A poem by @CorinaDuyn, an artist with #MyalgicE, summing up the unfortunate payback in the illness. From her book, Hatched, http://www.corinaduyn.com/site/buy-wellness-art-and-books-by-corina-duyn/hatched-re-hatched/ … (posted with permission) #MEcfs #CFS #MyalgicEncephalomyelitis

Chronically Hopeful‏  @chronic_hopeful 10h10 hours ago More The best advice I got when I was first diagnosed: listen to your body.  Symptoms are a sign something is wrong, it's not imaginary, you can't brush it off/will it away, you certainly shouldn't push through it either.  Rest, nourish, hydrate & rest some more. #mecfs #spoonie

Chronically Hopeful‏ @chronic_hopeful 10h10 hours ago More The best advice I got when I was first diagnosed: listen to your body. Symptoms are a sign something is wrong, it's not imaginary, you can't brush it off/will it away, you certainly shouldn't push through it either. Rest, nourish, hydrate & rest some more. #mecfs #spoonie

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