Raising Rare Raising Rare

Welcome back! We can’t believe we are already on our fifth season of Raising Rare. So much has happened since we started this podcast and we hope to keep evolving, growing, and bringing remarkable stories and individuals to all of our listeners.  
What words would you use to describe your hopes for the coming year (or coming season of Raising Rare)? After a short break our cohosts are back to talk about changes and mindsets they are having for the coming year.  
What are your goals for the coming year?
We would love to hear from you about any book recommendations, hopes for upcoming episodes, or any stories you may want to share. Please reach out to us on social media (add handles) or at office@salemoaks.com.
Resources From This Episode: Kristin Smedley - https://www.thrivingblindacademy.org/
Mentioned in this episode:
Invitation to Check Out The Atlas
The Atlas

On this episode in our Other End of the Tunnel Series we are joined by Mark Dant. When their son was just three years old, Mark and his wife were told that their son would pass within the decade after his diagnosis of MPS 1 and the lack of treatments available. As they laid on his floor listening to him breathe on the night of his diagnosis, they buried the home that might have been and the dreams of the life that was no longer possible. 
As Mark joins us today, his son is now 35, married, recently bought a home and is still having the journey that they never thought he would be able to experience.
What started as a bake sale raising just a few hundred dollars led them down a path that led to a scientist. Everything they did at the moment regardless of how small of insignificant it seemed, and over the next 30 years, culminated to what is happening now.  That scientist and his dedication led to a treatment just 8 weeks before Ryan’s 10th birthday that forever changed the course of their life. More importantly, that scientist has remained present in their lives throughout all of Ryan’s milestones. He was present at his High School graduation, his college graduation, and even recently at his wedding. That scientist’s dedication and commitment pushed the science to a treatment for Ryan and that treatment allowed the development of treatments for so many other children with similar rare diseases.

This episode we are joined by Aisling Finn, an amazing poet and rare disease mama. As she shares her poetry with us, we react to the emotions, struggles, key moments and pain that are so clearly pictured in her words. Aisling shares with us the impact that writing poetry has had on her, and her expression of her feelings, and how they have helped her cope with her own rare mama journey. 
Each of the poems that Aisling shares with us touches on a different impact of her life, stories that so many rare parents can relate to, understand, and feel the impact of. This episode is truly special.
Aisling’s poetry can be found on Amazon, Hope and Motherhood: Plot Twist.

On this episode of Raising Rare we talk with Megan Nolan, a rare mama working to make a difference for other Rare Families. Megan has launched the online magazine Rareparenting.com in an effort to provide rare families with resources that may be beneficial to them.  
Like so many other rare families, Megan has experienced the trials and tribulations of the healthcare system and how important it can be to move to the right location. She and her husband decided to use their skills and resources to build The Children’s Rare Disorders Fund (https://www.thecrdfund.org/) to help support R&D. She wants the fund to help small disease organizations work together and reduce duplication of effort. Listen along as our hosts discuss the different obstacles she has faced and why certain aspects of her son’s journey with FOXG1 have taken so long.
Mentioned in this episode:
Invitation to Check Out The Atlas
The Atlas

As Raising Rare continues to grow and evolve we are going to start bring in professionals that have beneficial stories for Rare Parents. These are individuals who have dedicated their lives to helping families in one aspect or another as they care for their children. Their viewpoints, stories, and perspectives are uniquely beneficial to parents that are involved in the rare community.
On this episode of Raising Rare we talk with Neil Ead, a 40 year veteran of the nursing field who has focused his career on pediatrics and more specifically chronic care. Neil discuses with our cohosts the importance of preparing in advance for the transition from pediatrics to adult care. This process includes finding replacements for most to all members of the care team and how hard this can be for the team members and the family. 
Mentioned in this episode:
Invitation to Check Out The Atlas
The Atlas

On this episode of Raising Rare we talk with Stacy Lloyd, a rare disease patient and board certified patient advocate. Stacy has dedicated her life, even much of her free time to healthcare in one way or another. She currently works at the American Medical Association, previously at Saavy Co-op, and is on the board of the VHL Alliance. After being diagnosed with Von Hippel-Lindau (VHL) at a young age, doctors told Stacy that she might not be able to walk as she got older and tumors continued to grow. She went on believing this for most of her early adult life and even admits that she never thought about retirement or other aspects of growing older because they just wouldn’t pertain to her. It wasn’t until 2018 that a doctor she met at a medical conference for VHL told her that she was going to be alright, she would be just fine, that she started to really consider her life.
Stacy’s diagnosis of having a rare genetic condition at an early age actually led to a number of her family members being diagnosed as well. Stacy speaks with us candidly that not everyone has handled their diagnosis with as much hope and drive as she has and that a number of factors have played into that. Stacy’s hope for members of the rare community is that everyone continues to share their stories, that they continue being vulnerable with each other and their medical team because you never know who will benefit from you doing so.
Mentioned in this episode:
Invitation to Check Out The Atlas
The Atlas