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İçerik Joanna tarafından sağlanmıştır. Bölümler, grafikler ve podcast açıklamaları dahil tüm podcast içeriği doğrudan Joanna veya podcast platform ortağı tarafından yüklenir ve sağlanır. Birinin telif hakkıyla korunan çalışmanızı izniniz olmadan kullandığını düşünüyorsanız burada https://tr.player.fm/legal özetlenen süreci takip edebilirsiniz.
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Superficial Siderosis With Rori From Texas

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Manage episode 450783249 series 3485028
İçerik Joanna tarafından sağlanmıştır. Bölümler, grafikler ve podcast açıklamaları dahil tüm podcast içeriği doğrudan Joanna veya podcast platform ortağı tarafından yüklenir ve sağlanır. Birinin telif hakkıyla korunan çalışmanızı izniniz olmadan kullandığını düşünüyorsanız burada https://tr.player.fm/legal özetlenen süreci takip edebilirsiniz.

Send us a text

In this episode of Rare Connection, Joanna sits down with Rori, Vice President of the Superficial Siderosis Research Alliance (SSRA), to explore the complexities of Superficial Siderosis (SS), a rare and progressive neurodegenerative condition. Together, they discuss:

  • The causes, symptoms, and diagnostic challenges of SS.
  • Current treatments like chelation therapy and the role of dietary considerations.
  • The vital work of the SSRA in advancing research and supporting patients.
  • The ongoing challenges of funding rare disease advocacy and research.

Whether you're living with SS, supporting a loved one, or simply curious about rare conditions, this episode shines a light on the importance of awareness, advocacy, and community.

👥 Guest Information:

  • Rori: Vice President of the Superficial Siderosis Research Alliance
  • Learn more about SSRA: SSRA.livingwithSS.org

🌟 Key Takeaways:

  • Understanding Superficial Siderosis: SS is caused by chronic bleeding into the brain or spinal cord, leading to iron buildup and damage to the nervous system.
  • Symptoms and Diagnosis: SS can present as hearing loss, ataxia, or cognitive changes, and is often misdiagnosed due to its rarity.
  • Treatment Options: Chelation therapy can help remove iron buildup, but early diagnosis is critical for managing symptoms.
  • The Role of Advocacy: SSRA connects patients, raises awareness, and drives research forward, highlighting the importance of collective effort in rare disease spaces.

📝 Episode Links & Resources:

  • Donate to the SSRA: SSRA.livingwithSS.org
  • Connect with Rare Connection:
    • Website: rareconnection.org
    • I am currently trying to turn Rare Connection into a Nonprofit and I need governing board members. Time commitment approximately 20 Hours a week. This is a volunteer job, so you won't be paid, I am looking for a secretary to take meeting minutes, lead the outreach committee as we grow, help with organization and newsletters, and the email list. I also need a treasurer, who is responsible for the financial end of things, budgeting, and leading the fundraising committee as we grow. Meeting time included in estimate. 1 to 2 hours a month committee time estimated between 2 and 4 hours, but it will take time to get that started. if interested email me at jball@rareconnection.org
  • I am looking to collaborate with medical professionals to offer CE Credits, if you are interested in showing my podcast in your classroom and offering CE credits for it please let me know. All guests are encouraged to bring visuals on to the visual part of this podcast.

Lastly, I am looking for sponsors if you are interested in sponsoring the show please reach out to me at jball

The Ryan Samuels Show
Modern-day politics discussion and analysis. Conservative Political Commentator Ryan...
Listen on: Apple Podcasts Spotify

& so much more
A bi-monthly podcast where we share the stories of our Caregivers, patients and...
Listen on: Apple Podcasts Spotify

Support the show

  continue reading

Bölümler

1. Superficial Siderosis With Rori From Texas (00:00:00)

2. [Ad] The Ryan Samuels Show (00:31:06)

3. (Cont.) Superficial Siderosis (00:31:55)

4. [Ad] & so much more (00:41:41)

5. (Cont.) Superficial Siderosis (00:42:31)

39 bölüm

Artwork
iconPaylaş
 
Manage episode 450783249 series 3485028
İçerik Joanna tarafından sağlanmıştır. Bölümler, grafikler ve podcast açıklamaları dahil tüm podcast içeriği doğrudan Joanna veya podcast platform ortağı tarafından yüklenir ve sağlanır. Birinin telif hakkıyla korunan çalışmanızı izniniz olmadan kullandığını düşünüyorsanız burada https://tr.player.fm/legal özetlenen süreci takip edebilirsiniz.

Send us a text

In this episode of Rare Connection, Joanna sits down with Rori, Vice President of the Superficial Siderosis Research Alliance (SSRA), to explore the complexities of Superficial Siderosis (SS), a rare and progressive neurodegenerative condition. Together, they discuss:

  • The causes, symptoms, and diagnostic challenges of SS.
  • Current treatments like chelation therapy and the role of dietary considerations.
  • The vital work of the SSRA in advancing research and supporting patients.
  • The ongoing challenges of funding rare disease advocacy and research.

Whether you're living with SS, supporting a loved one, or simply curious about rare conditions, this episode shines a light on the importance of awareness, advocacy, and community.

👥 Guest Information:

  • Rori: Vice President of the Superficial Siderosis Research Alliance
  • Learn more about SSRA: SSRA.livingwithSS.org

🌟 Key Takeaways:

  • Understanding Superficial Siderosis: SS is caused by chronic bleeding into the brain or spinal cord, leading to iron buildup and damage to the nervous system.
  • Symptoms and Diagnosis: SS can present as hearing loss, ataxia, or cognitive changes, and is often misdiagnosed due to its rarity.
  • Treatment Options: Chelation therapy can help remove iron buildup, but early diagnosis is critical for managing symptoms.
  • The Role of Advocacy: SSRA connects patients, raises awareness, and drives research forward, highlighting the importance of collective effort in rare disease spaces.

📝 Episode Links & Resources:

  • Donate to the SSRA: SSRA.livingwithSS.org
  • Connect with Rare Connection:
    • Website: rareconnection.org
    • I am currently trying to turn Rare Connection into a Nonprofit and I need governing board members. Time commitment approximately 20 Hours a week. This is a volunteer job, so you won't be paid, I am looking for a secretary to take meeting minutes, lead the outreach committee as we grow, help with organization and newsletters, and the email list. I also need a treasurer, who is responsible for the financial end of things, budgeting, and leading the fundraising committee as we grow. Meeting time included in estimate. 1 to 2 hours a month committee time estimated between 2 and 4 hours, but it will take time to get that started. if interested email me at jball@rareconnection.org
  • I am looking to collaborate with medical professionals to offer CE Credits, if you are interested in showing my podcast in your classroom and offering CE credits for it please let me know. All guests are encouraged to bring visuals on to the visual part of this podcast.

Lastly, I am looking for sponsors if you are interested in sponsoring the show please reach out to me at jball

The Ryan Samuels Show
Modern-day politics discussion and analysis. Conservative Political Commentator Ryan...
Listen on: Apple Podcasts Spotify

& so much more
A bi-monthly podcast where we share the stories of our Caregivers, patients and...
Listen on: Apple Podcasts Spotify

Support the show

  continue reading

Bölümler

1. Superficial Siderosis With Rori From Texas (00:00:00)

2. [Ad] The Ryan Samuels Show (00:31:06)

3. (Cont.) Superficial Siderosis (00:31:55)

4. [Ad] & so much more (00:41:41)

5. (Cont.) Superficial Siderosis (00:42:31)

39 bölüm

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