meaction.net

#MEAction | Fighting for health equality for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome

Clinicians & Researchers. Health Equality for ME. A global health network for people with Myalgic Encephalomyelitis, also known as chronic fatigue syndrome. Clinicians & Researchers. Here are some of our many community projects. Time For Unrest is a global impact campaign designed to strengthen the growing movement advocating for more recognition, education, research, and funding around ME. What happens when you have a disease doctors can't diagnose. Jen Brea presents at TED in June of 2017. The cause of...

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#MEAction | Fighting for health equality for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome | meaction.net Reviews

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Clinicians & Researchers. Health Equality for ME. A global health network for people with Myalgic Encephalomyelitis, also known as chronic fatigue syndrome. Clinicians & Researchers. Here are some of our many community projects. Time For Unrest is a global impact campaign designed to strengthen the growing movement advocating for more recognition, education, research, and funding around ME. What happens when you have a disease doctors can't diagnose. Jen Brea presents at TED in June of 2017. The cause of...

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#MEAction | Fighting for health equality for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome | meaction.net Reviews

https://meaction.net

Clinicians & Researchers. Health Equality for ME. A global health network for people with Myalgic Encephalomyelitis, also known as chronic fatigue syndrome. Clinicians & Researchers. Here are some of our many community projects. Time For Unrest is a global impact campaign designed to strengthen the growing movement advocating for more recognition, education, research, and funding around ME. What happens when you have a disease doctors can't diagnose. Jen Brea presents at TED in June of 2017. The cause of...

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stories.meaction.net

ME Stories | Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. March 27, 2016. I first saw a GP for post-exertional malaise about 6 months after my symptoms started following a nasty virus. She told me it was probably the menopause despite me having no other symptoms of this and. Read more →. They told me to do some exercise. March 27, 2016. Read more →. December 3, 2015. Read more →. Tale of an Invisible Illness. December 2, 2015. Read more →. November 11, 2015. I'm still und...

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meaction.net

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Facebook tiles | #MEAction – A platform for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome activism

https://www.meaction.net/facebook-tiles

Middle East & Africa. Reports and Fact Sheets. What is M.E? CLICK FOR THE FULL SIZE IMAGE. Save to your computer. Then upload it to your Facebook or Twitter page and share! Leave a Reply Cancel reply. Your email address will not be published. Required fields are marked *. Notify me of follow-up comments by email. Join a global movement for health equality. Reports and Fact Sheets. What is M.E?

2

Submit | #MEAction – A platform for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome activism

https://www.meaction.net/submit

Middle East & Africa. Reports and Fact Sheets. What is M.E? MEAction is designed to allow anyone to contribute content whether it’s an action. Or an opinion piece. Items posted here will be shared on Twitter. Select items will be shared with our global email list of over 12,000 subscribers. All content submitted will display your name or the name of your organization as the author (depending on your account. Preferences). Pseudonyms are allowed but real names are encouraged. Submit a news piece.

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Create a new action | #MEAction – A platform for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome activism

https://www.meaction.net/create-an-action

Middle East & Africa. Reports and Fact Sheets. What is M.E? Create a new action. Add your voice to a petition and leverage the power of this community. Search for open petitions or learn how to launch your own. Search for events in your area or learn how to organize your own #MEAction event. Have you already started a petition. Have you been approved for an event campaign. Or do you have a preexisting action hosted on your own webpage that you would like us to share? Submit news or opinion.

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Browse Actions: Petitions | #MEAction – A platform for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome activism

https://www.meaction.net/browse-actions-petitions

Middle East & Africa. Reports and Fact Sheets. What is M.E? Arts & Letters. New One Click Campaign. Ask NIH to fund an Ampligen Trial Today! NIH is asking the ME/CFS community what future research should be done. Below is a request to have NIH fund . UK: sign the petition close to forcing government response. A petition for more biomedical research funding for ME/CFS that was started in January is only 2,000 signatures short of . Petition: #MillionsMissing teams up with Mary Gelpi for research funding.

5

Start a Petition | #MEAction – A platform for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome activism

https://www.meaction.net/take-action/start-a-petition

Middle East & Africa. Reports and Fact Sheets. What is M.E? Want to start your own petition? Anyone can start a new individual petition. Submit your idea for a petition campaign. If you have your own concept for a petition campaign, you can suggest your idea by filling out this form. What is a petition campaign? Browse all current petitions. Launch a new petition. How to launch a Petition on #MEAction. How the Dutch petition got 56,000 signatures. How to organize a world-changing petition.

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stories.meaction.net

Submit your story | ME Stories

http://stories.meaction.net/submit-your-story

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. Thank you so much for the generosity of sharing your story so that others might learn from it and still others might heal from it. All of the fields below are optional. For example, you can submit your post with or without a title. You can submit only an image. You do not need to provide an author name if you do not want to be public; if left blank it will default to "anonymous.". Thank you for sharing your story!

stories.meaction.net

Mild ME | ME Stories

http://stories.meaction.net/category/mild-me

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. One small step for woman, one giant step for ME sufferer. November 4, 2015. I'm still undiagnosed. 20 years. I'm an all or nothing person. I go until I fall; or seizure (tonic clonic fits from extreme exertion) When I'm well I can't imagine being sick. When I'm sick I can't imagine what it's ….

stories.meaction.net

Uncategorized | ME Stories

http://stories.meaction.net/category/uncategorized

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. They told me to do some exercise. March 27, 2016.

stories.meaction.net

Medicine | ME Stories

http://stories.meaction.net/category/medicine

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. One small step for woman, one giant step for ME sufferer. November 4, 2015. I'm still undiagnosed. 20 years. I'm an all or nothing person. I go until I fall; or seizure (tonic clonic fits from extreme exertion) When I'm well I can't imagine being sick. When I'm sick I can't imagine what it's ….

stories.meaction.net

Tale of an Invisible Illness | ME Stories

http://stories.meaction.net/2015/12/02/tale-of-an-invisible-illness

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. Tale of an Invisible Illness. December 2, 2015. Today is my 18 month bed-iversary. I've spent at least 20 hours of the day in bed for the past 18 months. (I'm "celebrating" with chocolate mud cake and a soy latte a bit later, in case you're wondering). Then she then asked:. How do I go at the shops? Would I use a mobility scooter if I went to the shops? What if I want something from the shops? I understand that she...

stories.meaction.net

UK | ME Stories

http://stories.meaction.net/category/countries/uk

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. March 27, 2016. I first saw a GP for post-exertional malaise about 6 months after my symptoms started following a nasty virus. She told me it was probably the menopause despite me having no other symptoms of this and ran a very basic …. Graded Exercise Therapy Ruined ME. November 10, 2015.

stories.meaction.net

Severe ME | ME Stories

http://stories.meaction.net/category/severe-me

Share your experiences living with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome. Tale of an Invisible Illness. December 2, 2015. Today is my 18 month bed-iversary. I've spent at least 20 hours of the day in bed for the past 18 months. (I'm "celebrating" with chocolate mud cake and a soy latte a bit later, in case you're wondering). November 1, 2015. The walk was about a mile. As soon ….

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#MEAction | Fighting for health equality for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome

Clinicians & Researchers. Health Equality for ME. A global health network for people with Myalgic Encephalomyelitis, also known as chronic fatigue syndrome. Clinicians & Researchers. Here are some of our many community projects. Time For Unrest is a global impact campaign designed to strengthen the growing movement advocating for more recognition, education, research, and funding around ME. What happens when you have a disease doctors can't diagnose. Jen Brea presents at TED in June of 2017. The cause of...

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