The painting is by Francisco Goya, a self-portrait with the doctor who nursed him through a serious, life-threatening illness. The artist's inscription says 'Goya, in gratitude to his friend Arrieta: for the compassion and care with which he saved his life during the acute and dangerous illness he suffered towards the end of the year 1819 in his seventy-third year.' This is what so many of us with ME have wished for -- compassion and care.   Guest blog by Amy McLaughlin   One of the biggest casualties for me in a very long illness has been a loss of faith, not in any god, but in the integrity of our health care system, and in language itself, in the possibility of using words to successfully communicate something vital to others. No matter how hard I tried to describe my illness, how deep and tenacious its bite, how crushing the symptoms, people -- including, tragically, doctors -- are often skeptical.  This baffled me for a very long time, until I accepted how visual a species we are.  Like Othello, we want 'the ocular proof', and like Othello, we can be precipitate and destructive fools, easily misled by our confidence in what we think we see, and the rightness of our interpretations.  A central problem seems to be that I, and other patients with this disease, don't look the way sick people are expected to look.  Continue reading

May 12, 2022, marks the 30th anniversary of International Awareness Day for Complex Immunological & Neurological Diseases (CIND), and the 10th anniversary of May12.org. “If a cause and cure are to be found for ME, FM, MCS, GWI, Chronic Lyme Disease and other related C.I.N.D. illnesses in the near future, government and medicine must be made fully aware of their scope and impact. Despite the efforts of a number of dedicated groups and individuals, there are still vast pockets of ignorance and misunderstanding. To this day, many patients run directly into a medical establishment that, in general, knows very little about these serious threats to human health. It is therefore crucial that all those affected by the illnesses make their voices heard, especially on May 12th of each year.” Continue reading

Image from Anne Space Coast Photography Anne LiConti, a myalgic encephalomyelitis (ME) patient and advocate for more than 30 years, shares her story of diagnosis, challenges as well as how she found helpful treatments to improve her quality of life. She shares her story of survival and perseverance in a series of youtube videos answering our questions and giving insights into how she found hope after many years. Whether you are a newly diagnosed or long-term person with ME (pwme), a doctor, researcher, or just interested in the disease - you will gain much-needed information on what it means to be a long-term sufferer and clues as to what may be helpful in regaining some function. Continue reading

Myalgic Encephalomyelitis (ME) is a chronic, often severely disabling disease, that affects the autonomic nervous system, immune system, endocrine system, among others. It afflicts over one million men, women, and children in the United States alone and as many as 17 million worldwide. ME is a disease that robs individuals of their health, similar to untreated HIV. There are those that refer to ME as non-HIV AIDS - with good cause, as the disease can leave sufferers confined to a bed, with little capacity to fend for themselves. Continue reading

UPDATE: 5/5/2020 The Mel Robbins show is now scheduled to air the piece about the Remarkable Women on May 6, 2020. Find Mel Robbins show on these stations: https://www.melrobbinsshow.com/channels UPDATE: 3/25/2020 The Mel Robbins show scheduled to air the piece about the Remarkable Women has been postponed and will NOT air on March 26th. No new air date is scheduled. The organization indicated they hope to air this piece on the Mel Robbins show in May. UPDATE: 3/19/2020 Colleen was selected to represent her area and won the trip to New York City along with more than 100 other women. Due to COVID-19, the organizers cancelled the trip scheduled for the week of March 16 and cancelled taping on the Mel Robbins show. Instead, the videos of the women selected will be used to create a show which will air on the Mel Robbins show on March 26th. The top finalists and winner will be announced at that time. Find Mel Robbins show on these stations: https://www.melrobbinsshow.com/channels ______________________________________________________________________________________________________________________________     Continue reading

  Due to the hard work of Jim and Pam Lutey, Rotary International Board is considering a proposal to encourage research, education and funding for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). MEadvocacyOrg appreciates the advocacy efforts of the Luteys who initiated this proposal through their local Rotary in Colorado. Read about the proposal and what adoption by Rotary could mean for ME patients. Continue reading

Earlier this month, the myalgic encephalomyelitis (ME) community recognized Severe ME Day of Understanding and Awareness. Every day should be Severe ME Day - and at MEadvocacyOrg, that is exactly what we strive to do. August 8th - as a dedicated day to raise awareness of the plight of the severely affected ME patients - was conceived in 2013 by Diane, the mother of a severely affected ME patient, and was subsequently taken on by The 25% M.E. Group. Continue reading

On July 8, 2019, activist Eileen Holderman and Gabby Klein, met in Washington, DC with a Senior Advisor of the Office of Intergovernmental and External Affairs of the Department of Health and Human Services (HHS) to discuss the requests in the Open Letter to Secretary Azar and to deliver the petition approaching 7,000 signatures. You can read all the correspondence that led up to the meeting and the letter following the meeting with HHS here. Continue reading

  It has been 50 years since the World Health Organization classified myalgic encephalomyelitis (ME) as a neurological disease in 1969. Thirty plus years of misinformation about the harsh reality ME patients face has led to a crisis of grossly inadequate patient care. For decades patients have dealt with doctors who were given inaccurate information leading to denied disability claims and blaming patients for their symptoms. MEadvocacy was created to promote and educate for the distinct disease myalgic encephalomyelitis, including severe patients. The key to getting proper recognition and proper care in any disease is a clear description. Judging by what we are witnessing from the NIH and CDC, we have a long way to go before ME is properly recognized in the US. Continue reading

  GUEST BLOG - from May12.org May 12, 2019, marks the 27th anniversary of International Awareness Day for Complex Immunological & Neurological Diseases (CIND) and the 7th anniversary of May12.org. Continue reading