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Browse Actions: Severe ME

Support Severe ME Day: Join the Silence Challenge

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August 8th is Severe ME Day. It is a day of awareness raising for those suffering severe Myalgic Encephalomyelitis as well as a day of remembrance. August 8th was the birthday of Sophia Mirza, a 32 year-old woman who died of ME. One way you can participate and raise awareness for ...

Take Action on Severe ME Day

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Today, August 8th, is Severe ME day.  Today is a day of remembrance, when we think of those whom we have lost to ME.  Severe ME Day is August 8th because that was Sophia Mirza's birthday.  Her death in 2003 was one of the first in which cause of death ...

Send Dr. Ron Davis a 75th birthday message!

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The Open Medicine Foundation (OMF) is inviting patients and supporters to send Dr. Ron Davis a message for his birthday and a donation to support his End ME/CFS Project. The OMF said that the messages would be compiled into a “massive card” that would be presented to him. Dr. Davis, of Stanford ...

free patient conference call

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chat live with other pwme globally ...

Send Birthday Cards to Karina Hansen

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Editor's note: Karina Hansen is young Danish woman with severe ME. In February 2013, she was forcibly removed from her home by police and taken to a facility for functional (i.e,. psychosomatic) illnesses. The ME Alliance is organizing an action for Karina's third birthday away from home. You can help Karina ...

Petition: Get Sweden To Support International ME/CFS Projects

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I want Sweden to contribute to international research for ME / CFS – it will also help you! Sweden has about 40 000 people suffering from ME / CFS. I hope that Sweden can contribute to the Open Medicine Foundation and Lipkin / Hornig study ...

Sign a petition to Reinstate Federal Research Funding for ME/CFS

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Help Find a Cure for Whitney Dafoe and others like him! Hearing that funding has been reduced to nothing is heartbreaking. Please hear out these words from something who is suffering, and help him: ...

Life with M.E. – Short Film Fundraiser

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Change For M.E. Change For Us is creating a short film about discrimination and neglect that those living with M.E. must face every day in the medical community. Our volunteers are raring to go, now we just need vital funding.. ...

#myMEstory

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As part of the #chilliMEchallenge we are encouraging people to tell us their #myMEstory and create awareness by putting a voice and a face to this illness ...

Help 6000 ME/CFS sufferers in New Zealand get a field worker

We humbly ask for the community's help to fundraise for a field worker in Auckland, New Zealand. We hope to set a precedent for the international community, providing a platform for other countries to campaign for their own field workers ...