The passage of time does little to lessen the burden borne by a mother who香蕉视频直播檚 lost a child.

For Cheryl-Lynn Townsin, making a documentary after the death of her six-year-old daughter, Lexi, in 2019 from Blau Syndrome is about sharing stories of Lexi香蕉视频直播檚 battle and the struggles of other children with rare diseases.

香蕉视频直播淲e all have our ways of dealing with grief,香蕉视频直播� Townsin said. 香蕉视频直播淔or me it香蕉视频直播檚 about finding purpose. This film gave me the purpose to be able to tell the tragic story of Lexi to help others.香蕉视频直播�

Townsin completed RARE HUMANS - Turning Hope into Action as the capstone project for her Master of Arts degree in Global Leadership.

The documentary chronicles Lexi and the children in seven other families香蕉视频直播� trials, tribulations and triumphs as they cope with a variety of rare diseases. 香蕉视频直播淚 was also fortunate to interview the world香蕉视频直播檚 leaders in the rare disease community and to share their stories,香蕉视频直播� Townsin said. The release of the film coincided with Rare Disease Day on the last day of February, called the rarest day on the calendar.

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Townsin originally planned the film香蕉视频直播檚 focus to be on Lexi香蕉视频直播檚 battle with Blau Syndrome, which is believed to be caused by a gene mutation, with symptoms usually beginning to surface around the age of four. 香蕉视频直播淥nce I got started, I broadened the picture to include seven other families dealing with rare diseases.香蕉视频直播�

香蕉视频直播淓ight rare disease families in North America changing the future of medicine as they pursue their missions to cure the incurable,香蕉视频直播� is how Townsin described the project. 香蕉视频直播淭hese inspiring stories of love, loss and determination prove that every one of us has the ability to turn hope into action.香蕉视频直播�

The COVID-19 pandemic sidelined her plan to hold a symposium at Royal Roads University (RRU) with doctors from around the world who specialize in rare diseases, but Townsin did manage to connect with a number of global authorities. They include Dr. Ronald Cohen, the CEO of SickKids Hospital, renowned geneticist Dr. Donald Kohn from the University of California at Los Angeles, Dr. Durhane Wong-Rieger, president and CEO of the Canadian Organization for Rare Disorders, and Dr. Ann Pariser, director of the National Institute for Health/Office of Rare Disease Research in Bethesda, Maryland.

Half of the more than 400 million people who have rare diseases are children, Townsin noted. 香蕉视频直播淭hat香蕉视频直播檚 more than AIDS and cancer combined,香蕉视频直播� said Townsin, who has worked at RRU since 2004, most recently as student engagement co-ordinator.

香蕉视频直播淚t香蕉视频直播檚 a misnomer to call them rare diseases. Most people aren香蕉视频直播檛 aware that rare diseases are one of the leading causes of death, and 30 per cent of children with a rare disease will not live until their fifth birthday. These people are changing the future of medicine. Eighty per cent of rare diseases are genetic, so gene therapy offers the potential for finding a cure for so many diseases.香蕉视频直播�

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Townsin says the greatest challenges are raising awareness and securing funding for the research needed to find cures. Canada is one of the only developed countries with no framework for drugs for the treatment of rare diseases, she said, and research is hindered by the fact more funding is allocated globally to common diseases. She referenced a quote from Eli Pariser that illuminates one aspect of the issues:

香蕉视频直播淲e look at cancer as a leading example,香蕉视频直播� Pariser said. 香蕉视频直播淐ancer is not one disease. Cancer has hundreds of diseases and it may even be thousands of diseases as we start to unravel this, but cancer is a singular word that doesn香蕉视频直播檛 even have an 香蕉视频直播榮香蕉视频直播� on it and the cancer community has just done a fantastic job about speaking about cancer as one thing when it香蕉视频直播檚 not.香蕉视频直播�

香蕉视频直播淭he most eye-opening part of my research revolved around the work of Dr. Sidney Farber, who香蕉视频直播檚 known as the father of chemotherapy,香蕉视频直播� Townsin said. Farber realized they needed a poster child to promote unified support for dealing with the numerous types of childhood cancer and settled on a picture of a boy they called Jimmy that became synonymous with the movement.

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香蕉视频直播淚t changed the profile and dramatically improved funding,香蕉视频直播� Townsin said. She believes rare diseases need a similar approach and a unified voice like Farber advanced so successfully. 香蕉视频直播淚f you think of these diseases as rare, that undermines the significance of the problem,香蕉视频直播� she explained. 香蕉视频直播淲e need something dramatic like that to raise awareness and generate funding. We need these stories. That香蕉视频直播檚 the reason we decided to share Lexi香蕉视频直播檚 story and the stories of the other children in the film.香蕉视频直播�

For a trailer of the film, visit this The full documentary, to be distributed to film festivals around the world, is available free until the end of March .

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