Happy New Year!

We are so very excited for 2020! If you are a parent, patient, caregiver, donor, advocate or influencer, we are thrilled you are here and a part of our community. Our mission is to support our families affected by mitochondrial disease. Please reach out to us with any challenges or needs you may have. Here are the programs and events being offered the first part of the year: 

- Weekly Support Group Calls: Our calls with our Mitochondrial nurse, Marybeth Hollinger will resume Tuesday, January 7th. These calls are open to anyone impacted by mitochondrial disease; caregivers and patients. Toll free call in number is: 855-886-5126. Come join us for an open, insightful conversation.

- Monthly in-person support group lunches at Children's Colorado: Join us Tuesday, January 21st at Children's for lunch and conversation. Please RSVP if you can attend! 

- Grand Rounds on April 15th! Please stay tuned for this event with our Colorado Docs; Dr. Larson and Dr. VanHove. We are also thrilled to host Dr. Hirano from Columbia University department of Neurology. We are excited to sponsor this event in partnership with the UMDF. Further details to come! 

And in continuation of our support, if you live in the Rocky Mountain region extending from Montana to New Mexico, please contact us for needs outside of what is covered by medicaid and insurance. We are happy to sponsor a family grant, support ubiquninol needs or other supplements. 

We will be adding other events to the calendar as the year progresses. Please check in for updates. 

To an amazing 2020! 

Yours for a cure, 

Maria and Heather


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789 Sherman Street, Suite 250 Denver, CO 80203


Our mission is to educate the community about mitochondrial disease, provide support and resources to families affected by mitochondrial disease and provide opportunities and funding to transition research into treatments.