Myalgic encephalomyelitis has no standard diagnosis or cure, and yet there are 20 million sufferers in the world, with 30,000 of them being children in the UK alone. It receives little research funding from government agencies in the UK, USA, Europe and worldwide.
For over 25 years the research that has taken place has caused a renaming of the disease to Chronic Fatigue Syndrome, which instead of bringing clarity, has brought confusion breaking CFS into multiple diagnosis, of which none of them were physical.
This misrepresentation has continued on both sides of the Atlantic, and worldwide.
In 2007 in the US the Centre of Disease Control and Prevention formed an investigative panel which concluded CFS could be seen as a public health problem, while currently not seen as a priority.
Thousands signed petitions to ask the CDC to change their definitions. Meanwhile in the UK the recommended treatment for ME remains as Cognitive Behavioral Therapy,which is recommended from the psychiatric lobby for the NICE (National Institute of Health and Clinical Excellence) guidelines.
Today through controversy, intrigue, celebration and heartache the story of ME is developing with new research findings, making it more apparent that this is actually a transmissible disease, which could affect thousand if not millions more.
Our documentary follows a four year journey where our producer/director has followed a winding path to come up with her conclusion.
We at Doubled D Productions would like to thank all our generous contributors for their kind hearted support and positive energy throughout this campaign. Whilst we did not reach our target, we have connected with such an inspirational community across the continent which has only further fuelled our need to complete the documentary. The money raised will kick start filming in the UK, however with more developments coming through in Norway and again in the US, we will continue to seek more funding from alternative funding organisations.
Please keep following us via our facebook, and twitter as we will provide regular updates on our progress. We will not give up on this documentary and hope you all will continue to share the journey to finishing it with us!
Follow Us on Twitter @WHAT_ABOUT_M_E
- RT @velogubbed: @MEAssociation Is APPALLING this is situation 30 yrs after my own diagnosis. Shame on those medics&journalists who have neg… 26 days ago
- RT @MEAssociation: RT @MEAssociation: Health services research | NHS provision for pple severely affected by ME/CFS | 1 July 2014 http://t.… 26 days ago
- Let's get ME trending for #MEAwarenessDay! #MEcfs 77 days ago
- RT @actionforme: 87% of people with #MECFS are forced to stop/reduce paid work: read more in our #MEawarenessday report at http://t.co/8I9g … 77 days ago
- @5WrightStuff fantastic to see ME discussed on today's show! @Matthew_Wright raised the questions that the medical profession need to answer 77 days ago