Ashley and Megan continue their deep dive into the promising supplement, MitoKatlyst, by talking to Sundeep Dugar, co-founder of Blue Oak Nutraceuticals. Mitokatlyst is currently being used by many people diagnosed with mitochondrial disease, including Megan's son, Troy. Sundeep was American Chemical Society’s 2005 National Inventor of the Year and received the 2004 Heroes of Chemistry Award. He is co-author of 70+ publications and presentations, and co-inventor on 100+ issued and applied patents. Sundeep has also served as Trustee of the University of California Davis Foundation.

Blue Oak Nx is offering a special discount code to our listeners for Mitokatlyst purchases -- over $100 savings for each month supply. Use code "MitoPod225" - Use the single box option to make the purchase and add 3 or more boxes to your cart.

The Mito Podcast - a podcast for families and friends of children and adults with Mitochondrial Diseases and other rare diseases. We are two moms of Mito kids sharing support and resources and building community.

Listen to episodes and find us online:

Spotify

Apple Podcasts

YouTube

Facebook

Instagram

Menopause, Hormones and Mitochondria, oh my! Part 3 of 3 in Ashley and Megan's conversation with Monica and Sonya from Blue Oak Nutraceuticals about their promising Mitokatlyst supplement. They go deeper into the connection between hormones, menopause and mitochondrial function. Enjoy!

The Mito Podcast - a podcast for families and friends of children and adults with Mitochondrial Diseases and other rare diseases. We are two moms of Mito kids sharing support and resources and building community.

This is part 2 of a 3 part series where Ashley and Megan talk to Monica and Sonya, two of the founders of Blue Oak Nutraceuticals, about their new supplement called Mitokatlyst. Many mito families have been using this supplement and seeing positive health effects. In this episode they dive deeper into the science behind this supplement and its effects on mitochondria activity in cells.

*NOTE - Megan and Ashley are not affiliated with, or compensated by Blue Oak. In this discussion they want to shed light on the science and research behind supplement development and the science behind Mitokatlyst which is showing promising results for kids with mitochondrial disease.

The Mito Podcast - a podcast for families and friends of children and adults with Mitochondrial Diseases and other rare diseases. We are two moms of Mito kids sharing support and resources and building community.

It's been awhile, but Ashley and Megan are back with a new three part series of Mito Podcast episodes! In this series they talk to Monica and Sonya, two of the founders of Blue Oak Nutraceuticals, about their new supplement called Mitokatlyst. Many mito families have been using this supplement and seeing positive health effects.

*NOTE - Megan and Ashley are not affiliated with, or compensated by Blue Oak. In this discussion they want to shed light on the science and research behind supplement development and the science behind Mitokatlyst which is showing promising results for kids with mitochondrial disease.

In this episode, Megan and Ashley continue to talk about grief. Specifically - grieving the life you had planned before your child was diagnosed with a rare disease. While there is so much to be thankful for, parents still have to come to terms with the reality that the life they had imagined is forever changed.

This is a podcast for families and friends of children and adults with Mitochondrial Disease and other rare diseases. Two moms of Mito kids sharing support and resources and building community.

Also available on Apple, Google, Spotify and YouTube.

http://mitopodcast.com

Caring for children with rare diseases can be a 24/7 job that is often stressful and challenging for parents. Megan and Ashley share their perspectives on the importance of self-care for the parents and caregivers of special needs and medically fragile children.

This is a podcast for families and friends of children and adults with Mitochondrial Disease and other rare diseases. Two moms of Mito kids sharing support and resources and building community.

Also available on Apple, Google, Spotify and YouTube.

http://mitopodcast.com

In this episode Ashley talks to Megan about the recent loss of her sister-in-law Jen. Jen and Ashley's sisterJamila have two young children together. Ashley describes how the family is dealing with this tragic loss and how people handle grief in different ways.

Megan and Ashley are back after a little break! A quick update about what's been going on in their lives. Happy New Year!

This is a podcast for families and friends of children and adults with Mitochondrial Disease and other rare diseases. Two moms of Mito kids sharing support and resources and building community.

Also available on Apple, Google, Spotify and YouTube.

http://mitopodcast.com

Megan and Ashley have a great talk with April, who was diagnosed as an adult with a mitochondrial disease. She is a true Mito warrior and is currently writing her memoir. Find out more: https://www.facebook.com/chronicallyapril and https://aarguin.wixsite.com/website

This is a podcast for families and friends of children and adults with Mitochondrial Disease and other rare diseases. Two moms of Mito kids sharing support and resources and building community.

Also available on Apple, Google, Spotify and YouTube.

http://mitopodcast.com

Ashley and Megan talk to Sebastien of the Flowering Hope Foundation. His son, Jagger, has Leigh Syndrome, a mitochondrial disease. Sebastien shares his story, and his work in promoting information and research on the use of medical cannabis, which has been instrumental in reducing the number of daily seizures that Jagger suffers.

This is a podcast for families and friends of children and adults with Mitochondrial Disease and other rare diseases. Two moms of Mito kids sharing support and resources and building community.

Also available on Apple, Google, Spotify and YouTube.

http://mitopodcast.com