ME/CVS Stichting Nederland joins the World ME Alliance

This month, ME/CVS Stichting Nederland joined the World ME Alliance as a member. This Dutch organisation has been advocating for people with ME since 1987, and has a variety of focuses as they work to empower and improve the position of people with ME in the Netherlands. Their core focuses…

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ME CVS Nederland

Member ME/CVS Nederland is a Dutch charity working to empower and improve the position of people with ME in the Netherlands. They work to provide information, enable peer education, advocate to government and healthcare providers, and contribute to scientific research. Their board includes people with ME and carers, and they…

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Solve M.E. Advises and Reacts to Administration Reports on Long Covid

In April, President Biden issued a Presidential Memorandum directing the Secretary of Health and Human Services (HHS) to coordinate a new effort across the federal government to develop and issue... The post Solve M.E. Advises and Reacts to Administration Reports on Long Covid appeared first on Solve ME/CFS Initiative. Read…

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The Summer 2022 Edition of The Chronicle is Available Online Now!

The electronic version of our flagship research and advocacy journal, The Chronicle, has arrived! It includes a celebration of our Long Haul Voices: Living with Long Covid and ME/CFS video... The post The Summer 2022 Edition of The Chronicle is Available Online Now! appeared first on Solve ME/CFS Initiative. Read…

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The DHSC have released details of their process in the Development of a Delivery Plan on ME

On the 12 May, World ME Day, the former Secretary of State for Health and Social Care, Sajid Javid, announced the Government’s intention to develop a cross-Government Delivery Plan on ME/CFS for England. This intention was published in a Written Ministerial Statement laid in Parliament.  Development of the plan will…

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Delivery Plan on ME/CFS for England

DHSC Delivery Plan on ME/CFS development strategy   The Department for Health & Social Care (DHSC) in England has laid out the way they intend to develop the “cross-Government Delivery Plan on ME/CFS for England”, which their Health Secretary announced in May 2022. In a communication to stakeholders on 17th…

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Hear about research, services and future plans at our online AGM – Action for M.E.

All are welcome to attend Action for M.E.'s 2022 Annual General Meeting (AGM) where you can meet Action for M.E. staff and Trustees and hear how we’ve worked with and supported people…... This post appeared first on Action for M.E. Read more >>

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Consultation on Media Guidelines for M.E.

This consultation seeks feedback on suggested media advice for journalists reporting on M.E. and developing a helpful handbook of best practices for distribution to media outlets. The purpose of this consultation is to gather opinions from important stakeholders to ensure that all perspectives of the community are... This post appeared…

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Guest Blog: That Thing Called Pacing, by Ingebjørg Midsem Dahl

Ingebjørg Midsem Dahl was born in 1979 in Oslo, Norway, where she still lives. She came down with ME acutely in 1983. Ingebjørg has done written information work for major... The post Guest Blog: That Thing Called Pacing, by Ingebjørg Midsem Dahl appeared first on Solve ME/CFS Initiative. Read More…

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