When my son was first diagnosed with a RASopathy, a rare genetic syndrome that affects cell growth and cell regulation by virtue of affecting the RAS/MAPK signaling pathway, I was so excited to finally have a diagnosis. That was quickly replaced by despair. In my hand was a handwritten note listing the next 10 specialists we needed to see. I was given no other direction on where to find accurate information about the disease, support groups, or other families who might be in similar situations. There were no t-shirts or bumper stickers to purchase so I could proudly show my support.

As a parent faced with such a daunting diagnosis, I wanted to do something to make a difference, but I really didn’t know where to start. So I started simple. I created a t-shirt to sell. My goal was to raise funds for research. Little did I know it takes over 2 BILLION dollars to create a treatment. Since then, I’ve upgraded my efforts and moved from t-shirts to bike rides. I’m working hard, in my own small way, to raise funds for RASopathies research.  But there is still so much more we can do to facilitate rare disease research. Below are a few tips for those just entering the world of rare disease advocacy.

1. Participate in (or create) an online community specific to your rare disease

Join or build a community where those affected by a rare disease can talk to each other. Many of these groups, like the one I belong to, are for patients, parents, and caregivers. They need a safe space to share/critique treatment ideas, clinicians to see, and helpful daily living tips. It can also be a place for advocates to vent their concerns and celebrate their victories among their peers. My RASopathies online family has become my extended family. Being part of that group has taught me so much—especially regarding the sorts of issues current research efforts are not addressing.

2. Participate in research

Many clinical trials fail because of lack of recruitment. If you want better treatments, then participate in a research. Before doing so however, you need to do your research. First, talk to your doctor or do online research on clinicaltrials.gov to see if there are any clinical trials looking for research participants. You can also reach out to the researchers directly. Remember that journal search you did a few weeks ago on the disease and all those doctors that showed up on PubMed? Go back to that search, find those researchers, and email them directly to see if they know of any ongoing research studies that you might join or if they are looking for cell or tissue samples.

I understand not wanting your child to be a guinea pig. My son is poked and prodded enough. To be as efficient as possible and still participate in research, I try to coordinate research donations when my son will be sedated for another procedure. It only takes a few phone calls and emails to coordinate, and it feels good to know that you are contributing to the advancement of research for future innovative and more accessible treatments.

I am also involved with the  RASopathies Network USA,(https://rasopathiesnet.org).  A non-profit dedicated to advancing research of the RASopathies by bringing together families, clinicians, and scientists. Our biennial symposium(https://rasopathiesnet.org/rasopathies/meetings/2015-symposium/) provides a venue for a scientific collaboration between clinicians, researchers, trainees and affected families to share and discuss clinical issues, the science behind them, and develop a framework for future research. Dedicating your life to tackle rare disease issues isn’t for everyone but it helps me cope with not being able to alleviate my son’s struggles. My goal is that others will not have to go down the same path, or if they do, know that I helped make it a bit more manageable.

Read more at the source.

Lisa Schill is a parent advocate, dedicated to improving the lives of those living with rare diseases. Ms. Schill specializes in connecting caregivers, researchers, support organizations and families to help support patients in the pursuit of advancing treatment options and patient outcomes. She currently serves as Vice President of the RASopathies Network, a non-profit dedicated to advancing research of the RASopathies by bringing together families, clinicians and scientists. She is currently working as a Meetup Advocacy Ambassador for Global Genes facilitating rare disease meet ups for the aHUS (Atypical Hemolytic-Uremic Syndrome) population. She is a co-investigator for the 2015 International Meeting on the Genetic Syndromes on the RAS/MAPk Pathway to be held in Seattle, WA with the co-chairs, Drs. David Stevenson and Brigitte Widemann.

 

1 thought on “Rare Disease Advocacy: More Than Just Selling T-Shirts”

  1. Henryswipes says:

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