May 12 ME Awareness Day! Read about the history of May 12, see the projects that ME International provide for needy ME patients, and DONATE to help us assist more ME patients in need. Please share with family and friends.
https://t.co/kgquNmzmD3
Wishing our Jewish members globally a Happy Passover.
May this Passover be a time of Renewal, Blossoming and all good things.
Thank you for being a part of our community,
ME International
https://t.co/tEJmWYS7dH
April 2023 Newsletter
https://t.co/pF2kajqGuB
INCLUDES:
Proposal to add PEM/PESE to US diagnosis codes - comments needed by May 5.
Australian study using #MEICC needs participants ASAP.
Join mailing list here: https://t.co/fU6IgO744G
#MyalgicEncephalomyelitis#pwME
Please check out the article that Colleen & I co-wrote alerting the ME community to the potential harms of the proposal by the orgs to CDC. Sending thanks to Rob & the ME Global Chronicle team for highlighting our Call to Action!
https://t.co/kdN9aAqvse
⚠️Important update:
CDC's Traci Ramirez clarifies a May 5 deadline for public comments on proposal to add code for Post-exertional malaise/post-exertional symptom exacerbation to ICD-10-CM.
Proposal is NOT being considered for early implementation:
https://t.co/VS6rYMqzDT
@dxrevisionwatch Thank you for this update, Suzy! And thanks to David from ME International @ME_Intl for verifying that the deadline to submit comments remains May 5, which is good news for ME patients + advocates who require more time due to health considerations.
March 2023 Newsletter
https://t.co/gxuVYsi5Dx
A monthly newsletter bringing news from around the world to the #MyalgicEncephalomyelitis community.
Learn more at https://t.co/tEJmWYS7dH
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1⃣Update on request to add a Symptoms, signs code for Post-exertional malaise [PEM] to ICD-10-CM:
Lisa McCorkell (rep: Patient-Led Research Collaborative) confirmed yesterday that there have been some changes to the proposal since first submitted for consideration in June 2022.
It’s National Love your Pet Day, in a number of countries today. A lot of us in the #MyalgicEncephalomyelitis community have pets in our families, keeping us company through bad times and good, always giving us support.
Show us your pet pics!
#MEI#ME#pwME#MEcommunity
ME International will continue to fight for the rights of people with #MyalgicEncephalomyelitis, to have #ME understood as a #neuroimmune disease, and for access to fair and effective medical care for us all.
Help educate medical community w/ #ICP here: https://t.co/0MnlX7mrZN
Hoy han comparecido ante la comisión d sanidad d Euskadi asociaciones d SFC/EM
Antes @ME_Intl se ha reunido con Ibai Iriarte y @RebekaUbera dando voz a las personas con #Encefalomielitismialgica
Solicitamos herramientas diagnósticas y unidad interdisciplinar a @osakidetzaEJGV
@Ekhi_sasienGain @KCSteckel @ME_Intl @RebekaUbera@osakidetzaEJGV Lo tengo preparado para llevárselo mañana a mi médico de Atención Primaria 😉. Lo vuelvo a poner aquí a disposición de quien lo quiera, desde la web de @ME_Intl ⬇️
https://t.co/Bc7CViGUbq
@sfcem_mexico@carol_perelman@fcowester@_diatoma @ME_Intl ofrece mucha información con traducción rápida y revisada y documentos descargables traducidos al español en esta sección:
https://t.co/AFhc54y7G1
Espero que sea de vuestro interés