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My rare disease podcast

WebOnce Upon A Gene Podcast. Once Upon a Gene is a podcast that explores the world of raising children with disabilities and rare genetic disorders. Host, Effie Parks shares her own personal story of raising a child with CTNNB1 syndrome, while trying to find the non-existent rule book of bringing up such a special kid. WebFeb 28, 2024 · The 2024 Emmy-nominated Rare in Common documentary gave people from the rare disease community an opportunity to tell their stories. Today, the storytelling has expanded to the world of audio with the Rare in Common podcast. Whether you watch or listen, prepare to be moved and inspired by those touched by rare disease.

Effie Parks on LinkedIn: Once Upon A Gene- Rare Disease Podcast

WebJan 27, 2024 · My rare disease podcast to my rare disease products! We got to catch up with the wonderful rare disease advocate and youth team ambassador Katy Baker as she … WebBuild a beautiful podcast website in 5 minutes Automatically create a beautiful, listener-friendly podcast site from your RSS feed. ... 20 Dec 2024 · My rare disease . 00:31:29; This episode features Katie who has EDS and CIPO and we discuss what it means to have a good transition in hospital, the barriers a wheelchair user faced in both ... oxfordshire villages to visit https://earnwithpam.com

Takeda Launched ‘Amplify’ Podcast Series to Help Support …

WebWelcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health … Web*Podcast Host * Once Upon A Gene* Mom to a Rare Disease Warrior with CTNNB1 6d WebPresident at CTNNB1 Syndrome Awareness Worldwide (CSAW) Segnala post Segnala Segnala oxfordshire vineyard

My rare disease - Podcast trailer by My rare disease

Category:Rare Disease Report Podcast: CDKL5 Deficiency Disorder

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My rare disease podcast

My rare disease Podcast on Podbay

WebThe Rare Disorder Podcast hosted by Shivani Vyas. 21 episodes to date. Atypical Truth hosted by Erica Stearns, a disabled adult, and proud mother of two young children who … WebWelcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health professionals and advocates, we talk about all aspects of rare disease including relationships, mental health and much more.

My rare disease podcast

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WebWelcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health … WebPresident at CTNNB1 Syndrome Awareness Worldwide (CSAW) Report this post Report Report

WebWelcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health … WebApr 11, 2024 · In August 2024, I created my podcast ‘my rare disease’ with the aim of raising awareness of different rare conditions and sharing important messages. I want people to know that rare conditions can be so much more than a physical diagnosis, it can affect all aspects of a person’s life. This podcast has allowed me to have a voice and give a ...

WebMar 6, 2024 · The mission of our podcast is to support you, our listeners and to create community, as you confront the toughest challenges in life. All of us will experience health hardships. The real question is how we adapt. That is the focus of It Happened To Me, which wants to help you overcome limitations and live a full and satisfying life. WebApr 23, 2024 · My Rare Disease by Katy Baker On this podcast, the host, who was diagnosed with a rare disease as an infant, chats with other rare disease patients, health professionals, and advocates to talk about all aspects of rare disease. They discuss relationships, mental health, and much more.

WebWelcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 15 people, rare disease. By chatting to patients, health …

WebRare Disease Podcast Effie Parks February 17, 2024 Rare Disease, Special Needs Podcast. ONCE UPON A GENE - EPISODE 173 - Honoring a Husband’s Legacy by Finishing His Work on a Documentary About Rare Disease Acute Flaccid Myelitis and Her Own Grief Along the Way with Sarah Potter. jefferson city mo to amarilloWebWelcome to 'My rare disease' podcast. This is a platform where I raise awareness of something that affects 1 in 17 people, rare disease. By chatting to patient… jefferson city mo to breese ilWebIn our new monthly podcast, Rare on Air, our Communications Manager, Julien Poulain, meets with people who live with a rare disease, those who advocate for them, and experts on rare disease policy. The podcast explores the unique experiences, challenges and successes of people from our community, and investigates how we can build a better […] jefferson city mo things to doWebRare Disease Podcasts Two Disabled Dudes: Life Beyond Circumstances. Sean and Kyle are both affected by a rare disease called Friedreich’s... Two Rare Mama Bears. Two Rare … oxfordshire volunteering opportunitiesWebApr 12, 2024 · The series invites a global panel of patient group representatives, clinicians and policy makers in the rare bleeding disorders community to discuss how multiple stakeholders can work together to advocate for personalized care, with the goal of improving patient outcomes such as joint health. oxfordshire volunteersWebRare Disease Podcast. Starting listening to a few episodes of My Rare Disease Podcast where in each episode a person with a different rare disease is interviewed and talks about life. I thought it was a cool initiative of this young woman and that it … oxfordshire volunteeringWebAnunț publicat de Mariana Parks Mariana Parks President at CTNNB1 Syndrome Awareness Worldwide (CSAW) jefferson city mo to hazelwood mo