#HOMECFS - Twitter Hashtag

over 6 years ago

This is Stephanie S. Many #pwME need a more efficient way to receive a proper diagnosis so that their quality of life can be better, sooner. For Stephanie's story, click here https://t.co/xMhIVZH1PE #MECFS #HOMECFS

PlzSolveCFS's tweet photo. This is Stephanie S. Many #pwME need a more efficient way to receive a proper diagnosis so that their quality of life can be better, sooner.

For Stephanie's story, click here
https://t.co/xMhIVZH1PE
#MECFS #HOMECFS https://t.co/OYI94AbA8N

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Solve ME/CFS Initiative @PlzSolveCFS

over 6 years ago

This is Alice T. Many #pwME need a more efficient way to receive a proper diagnosis so that their quality of life can be better, sooner. Alice needed accurate results sooner. #SolveME. For Alice's story, click here https://t.co/oXjq14CGHV #MECFS #HOMECFS #MEawarenesshour

PlzSolveCFS's tweet photo. This is Alice T. Many #pwME need a more efficient way to receive a proper diagnosis so that their quality of life can be better, sooner. Alice needed accurate results sooner. #SolveME.

For Alice's story, click here
https://t.co/oXjq14CGHV
#MECFS #HOMECFS #MEawarenesshour https://t.co/IKfLuJrBAg

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Solve ME/CFS Initiative @PlzSolveCFS

over 6 years ago

This is Peter Y. Like him, many people need a more efficient way to receive a proper diagnosis so that their quality of life can be better, sooner. We aim for results. We aim to #SolveME. For Peter's story, click here https://t.co/sX3TaQEsAp #MECFS #HOMECFS #MEawarenesshour

PlzSolveCFS's tweet photo. This is Peter Y. Like him, many people need a more efficient way to receive a proper diagnosis so that their quality of life can be better, sooner. We aim for results. We aim to #SolveME.

For Peter's story, click here
https://t.co/sX3TaQEsAp
#MECFS #HOMECFS #MEawarenesshour https://t.co/Gbv1nMrSpe

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Solve ME/CFS Initiative @PlzSolveCFS

over 6 years ago

This is Anne B. We want her to be well with the ability to reconnect to all the events and activities she loves. We want her quality of life to be at its best. We aim to #SolveME. For her complete story, click here https://t.co/ilvlca31qM #MECFS #chronicillness #HOMECFS

PlzSolveCFS's tweet photo. This is Anne B. We want her to be well with the ability to reconnect to all the events and activities she loves. We want her quality of life to be at its best. We aim to #SolveME.

For her complete story, click here
https://t.co/ilvlca31qM
#MECFS #chronicillness #HOMECFS https://t.co/mxsGe0mHyK

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Solve ME/CFS Initiative @PlzSolveCFS

over 6 years ago

National Photographic Society's 'Photographer of the Year' in 2019 Angi Wallace uses her fantastic vision for beauty and photography to remind herself and world that's she's more than just a person with ME #pwME #Patientvoices #art #NPS #SolveME #HOMECFS https://t.co/nQOA29JPUf

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Solve ME/CFS Initiative @PlzSolveCFS

over 6 years ago

#MECFS changes lives. This chronic disease can strike anyone at any time, & is different in everyone. Some have debilitating exhaustion, others suffer from insomnia. Others have terrible joint pain. And some people have every symptom imaginable. #HOMECFS https://t.co/2rwZtKQWbj

PlzSolveCFS's tweet photo. #MECFS changes lives. This chronic disease can strike anyone at any time, & is different in everyone. Some have debilitating exhaustion, others suffer from insomnia. Others have terrible joint pain. And some people have every symptom imaginable. #HOMECFS https://t.co/2rwZtKQWbj https://t.co/G0OF5EIQRw

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Solve ME/CFS Initiative @PlzSolveCFS

over 6 years ago

The chronic exhaustion, weakened muscles, and aches and pains accompanying ME/CFS are completely debilitating. There is no FDA-approved treatment, and patients often suffer for life. But we still find ways to move forward. #MECFS #HOMECFS https://t.co/ftAQDrHm7l

PlzSolveCFS's tweet photo. The chronic exhaustion, weakened muscles, and aches and pains accompanying ME/CFS are completely debilitating. There is no FDA-approved treatment, and patients often suffer for life. But we still find ways to move forward. #MECFS #HOMECFS

https://t.co/ftAQDrHm7l https://t.co/KSKrIXgI4e

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Solve ME/CFS Initiative @PlzSolveCFS

almost 7 years ago

Humans of ME/CFS: Cindy B. To read her full story, follow the link below: https://t.co/TgG6ZR09rW #HOMECFS #invisibleillness #chronicillness #MECFS

PlzSolveCFS's tweet photo. Humans of ME/CFS: Cindy B.

To read her full story, follow the link below:
https://t.co/TgG6ZR09rW

#HOMECFS #invisibleillness #chronicillness #MECFS https://t.co/59Hv1Zbpd4

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Solve ME/CFS Initiative @PlzSolveCFS

almost 7 years ago

Humans of ME/CFS: Julie C. To read her full story, follow the link below. https://t.co/MNtafzYXVr #HOMECFS #invisibleillness #chronicillness #MECFS

PlzSolveCFS's tweet photo. Humans of ME/CFS: Julie C.
To read her full story, follow the link below.

https://t.co/MNtafzYXVr
#HOMECFS #invisibleillness #chronicillness #MECFS https://t.co/IQs4MTE7By

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Solve ME/CFS Initiative @PlzSolveCFS

about 7 years ago

Humans of ME/CFS: Deborah M. To read her complete story, follow the link. https://t.co/FOpeT2VFzi #MEawareness #MyalgicE #SevereME #pwME #MEcfs #MyalgicEncephalomyelitis #MillionsMissing #CanYouSeeMEnow #EndMEcfs #spoonie #HOMECFS #invisibleillness

PlzSolveCFS's tweet photo. Humans of ME/CFS: Deborah M. To read her complete story, follow the link. https://t.co/FOpeT2VFzi #MEawareness #MyalgicE #SevereME #pwME #MEcfs #MyalgicEncephalomyelitis #MillionsMissing #CanYouSeeMEnow #EndMEcfs #spoonie #HOMECFS #invisibleillness https://t.co/IgkD0oYygA

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Solve ME/CFS Initiative @PlzSolveCFS

about 7 years ago

Lori J. Humans of ME/CFS. To read her complete story, follow the link to https://t.co/qPrZ8YFAuZ #PWME #HOMECFS #invisibleillness #SolveME @PlzSolveCFS

PlzSolveCFS's tweet photo. Lori J. Humans of ME/CFS. To read her complete story, follow the link to https://t.co/qPrZ8YFAuZ #PWME #HOMECFS #invisibleillness #SolveME
@PlzSolveCFS https://t.co/6Wgnm3LzC5

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Solve ME/CFS Initiative @PlzSolveCFS

about 7 years ago

Emily Taylor writes to the United States Access Board and asks for additional research regarding current accessibility guidelines and their effectiveness in addressing the needs of up to 2.5 million Americans with #MECFS https://t.co/I3JBp7DEDh #PWME #CFS #MyalgicE #HOMECFS

PlzSolveCFS's tweet photo. Emily Taylor writes to the United States Access Board and asks for additional research regarding current accessibility guidelines and their effectiveness in addressing the needs of up to 2.5 million Americans with #MECFS https://t.co/I3JBp7DEDh #PWME #CFS #MyalgicE #HOMECFS https://t.co/P3O6NK1byA

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Solve ME/CFS Initiative @PlzSolveCFS

about 7 years ago

Kelly S. Humans of ME/CFS. To read her complete story, follow the link to https://t.co/e3BqYpc4Hr #MECFS #PWME #HOMECFS #invisibleillness #SolveME @PlzSolveCFS

PlzSolveCFS's tweet photo. Kelly S. Humans of ME/CFS. To read her complete story, follow the link to https://t.co/e3BqYpc4Hr
#MECFS #PWME #HOMECFS #invisibleillness #SolveME @PlzSolveCFS https://t.co/TIT4cB2dFw

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Solve ME/CFS Initiative @PlzSolveCFS

over 7 years ago

"I have many friends with ME/CFS both visible and on the internet such as Facebook. I am so sad for those who are house and bed bound and I am angry about the PACE Trials and the psychiatric lobby on ME/CFS." Read Keith's #HOMECFS story at, https://t.co/0cvf6oJvgX #MECFS

PlzSolveCFS's tweet photo. "I have many friends with ME/CFS both visible and on the internet such as Facebook. I am so sad for those who are house and bed bound and I am angry about the PACE Trials and the psychiatric lobby on ME/CFS."

Read Keith's #HOMECFS story at, https://t.co/0cvf6oJvgX #MECFS https://t.co/dAUz0VKnEv

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Solve ME/CFS Initiative @PlzSolveCFS

over 7 years ago

"I'm a shell of who I once was. I've made it my mission to create a new normal and bring awareness to our illnesses in the hopes of a cure one day." Read Donni's story at, https://t.co/JFWPfeZP4Q #MECFS #HOMECFS

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Solve ME/CFS Initiative @PlzSolveCFS

over 7 years ago

"I was an elementary school music teacher, community volunteer, church pianist, wife, and young mother when I became ill in March, 2000." Read Camille's story at, https://t.co/sZ7zYoRLbT #HOMECFS #MECFS

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Solve ME/CFS Initiative @PlzSolveCFS

almost 8 years ago

"I feel I've missed out on so much. I lost my way and got extremely depressed. Sometimes, I went days without eating or showering because the strain to stay awake and upright outweighed anything else." Read Lynne's #HOMECFS story at https://t.co/MOmS7ToT3R #MECFS

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Solve ME/CFS Initiative @PlzSolveCFS

almost 8 years ago

"I don't want to rest in the bed in the evening while my children are playing downstairs with their father." Read Camilla's at, https://t.co/IFDwWIUSds #MECFS #HOMECFS

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Solve ME/CFS Initiative @PlzSolveCFS

almost 8 years ago

"So now, at 55, I am going to have to figure out life on my own with severe disabilities. Am I scared? Out of my wits!" Read Kristina's story at https://t.co/ziTqLCIar8 #MECFS #HOMECFS

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Solve ME/CFS Initiative @PlzSolveCFS

almost 8 years ago

"Then along came ME/CFS, a nasty disease that took away our life of ease." Read Cheryl's story at, https://t.co/2JANi7gTJB #MECFS #HOMECFS

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