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Long Chain Hydrocxy Coenzyme A Dehydrogenase Deficiency (LCHAD)

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Manage episode 436239847 series 3485028
Konten disediakan oleh Joanna. Semua konten podcast termasuk episode, grafik, dan deskripsi podcast diunggah dan disediakan langsung oleh Joanna atau mitra platform podcast mereka. Jika Anda yakin seseorang menggunakan karya berhak cipta Anda tanpa izin, Anda dapat mengikuti proses yang diuraikan di sini https://id.player.fm/legal.

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This week Rare Connection goes back to it's roots with a condition covered by the Medical Nutrition Equity Act if it were to pass. The MNEA would mandate that health insurance cover medically prescribed food, formula and vitamins for those who need them. At the beginning of last season in February Nutrition Equity became Rare Conne6892ction to cover more conditions and allow me to go outside the country. House bill 6892 was reintroduced into congress by representative McGovern.
Long Chain Hydroxy Coenzyme A Dehydrogenase Deficiency (LCHAD) is an Inborn Error in Metabolism. Join me as I talk to Alexandra about how she was diagnosed, her podcast "Positively Walking with Mito<" Advocacy, Advice and hopes for the future as well as the Medical Nutrition Equity Act and how it would help those with LCHAD.
We are currently seeking a Senate Republican to champion the senate side. If you are in the US you can help us to get this bill passed for countless individuals. 12 episodes of Nutrition Equity were filmed before it became Rare Connection. We also now have a website. rareconnection.org If you are interested you can join our email list, read about our board members that currently have bios up, and more. Some of the episodes and shorts are also on their.
I am in the process of turning Rare Connection into a nonprofit, but I currently don't have all of the paperwork filed with the state and feds to do so. Your support is greatly appreciated, please click on the support the show link to support us. The podcast is monetized, I am also a caregiver and a rare disease advocate. I have an inborn error in Metabolism, a genetic condition called Homocystinuria which is related to PKU by diet, and (we follow a low protein diet because of a problem with a different essential amino acid) It looks more like Marfan's Syndrome and is commonly mistaken for it though. You can also text me through the link in the show notes. If you have a business I could also use sponsors. Thank you for your continued support.

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Chapter

1. Long Chain Hydrocxy Coenzyme A Dehydrogenase Deficiency (LCHAD) (00:00:00)

2. [Ad] PodMatch (00:13:43)

3. (Cont.) Long Chain Hydrocxy Coenzyme A Dehydrogenase Deficiency (LCHAD) (00:14:22)

32 episode

Artwork
iconBagikan
 
Manage episode 436239847 series 3485028
Konten disediakan oleh Joanna. Semua konten podcast termasuk episode, grafik, dan deskripsi podcast diunggah dan disediakan langsung oleh Joanna atau mitra platform podcast mereka. Jika Anda yakin seseorang menggunakan karya berhak cipta Anda tanpa izin, Anda dapat mengikuti proses yang diuraikan di sini https://id.player.fm/legal.

Send us a text

This week Rare Connection goes back to it's roots with a condition covered by the Medical Nutrition Equity Act if it were to pass. The MNEA would mandate that health insurance cover medically prescribed food, formula and vitamins for those who need them. At the beginning of last season in February Nutrition Equity became Rare Conne6892ction to cover more conditions and allow me to go outside the country. House bill 6892 was reintroduced into congress by representative McGovern.
Long Chain Hydroxy Coenzyme A Dehydrogenase Deficiency (LCHAD) is an Inborn Error in Metabolism. Join me as I talk to Alexandra about how she was diagnosed, her podcast "Positively Walking with Mito<" Advocacy, Advice and hopes for the future as well as the Medical Nutrition Equity Act and how it would help those with LCHAD.
We are currently seeking a Senate Republican to champion the senate side. If you are in the US you can help us to get this bill passed for countless individuals. 12 episodes of Nutrition Equity were filmed before it became Rare Connection. We also now have a website. rareconnection.org If you are interested you can join our email list, read about our board members that currently have bios up, and more. Some of the episodes and shorts are also on their.
I am in the process of turning Rare Connection into a nonprofit, but I currently don't have all of the paperwork filed with the state and feds to do so. Your support is greatly appreciated, please click on the support the show link to support us. The podcast is monetized, I am also a caregiver and a rare disease advocate. I have an inborn error in Metabolism, a genetic condition called Homocystinuria which is related to PKU by diet, and (we follow a low protein diet because of a problem with a different essential amino acid) It looks more like Marfan's Syndrome and is commonly mistaken for it though. You can also text me through the link in the show notes. If you have a business I could also use sponsors. Thank you for your continued support.

PodMatch
PodMatch Automatically Matches Ideal Podcast Guests and Hosts For Interviews
Support the show

  continue reading

Chapter

1. Long Chain Hydrocxy Coenzyme A Dehydrogenase Deficiency (LCHAD) (00:00:00)

2. [Ad] PodMatch (00:13:43)

3. (Cont.) Long Chain Hydrocxy Coenzyme A Dehydrogenase Deficiency (LCHAD) (00:14:22)

32 episode

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