Be Unique, Rare Disease

Updated: Oct 24, 2019


Hugs For Mito is a nonprofit ADVOCATING for Mitochondrial and Rare Diseases. We create AWARENESS and FUNDRAISE for clinics, research, trials and hopefully cures worldwide.

What makes us unique is our support for clinicians. Please help us support the amazing Mitochondrial Care network (MCN).

The MCN is a network of expert mitochondrial disease centers staffed by clinical directors with many years of experience in mitochondrial medicine and the ability to provide comprehensive mitochondrial disease medical care and diagnosis. The MCN is working towards developing centers with extensive multidisciplinary care for suspected and confirmed mitochondrial disease patients and their families.

We support Dr. Amel Karaa at Massachusetts General Hospital, Boston, MA. She’s a geneticist and researcher. Who will you support?

There are 18 member centers and 3 affiliate clinics.

We support the goal that each site should include Doctor’s and Ancillary Staff to help patients with all aspects of their disease burden (meal design, lifestyle design, social problems. . . We want to improve the quality of life for patients battling Mitochondrial Diseases and RARE (Complex) DISEASES everywhere.

Help us achieve this goal!

PLEASE LIKE, LOVE and share, share, share!

You can also donate directly on the Hugs For Mito website or support in any other way you can.


Hugs For Mito is a 501(c)(3) nonprofit ADVOCATING for Mitochondrial Disease and Rare Disease.

Help Us Give Strength

Motivate & Inspire To Overcome

1/10 People Are Affected By Rare Disease.

LOVE, Michael

Michael Goldberg

Hugs For Mito, Inc.

501(c)(3) Non-Profit

15 Lamplighter Lane

South Easton, MA 02375





Help Us Give Strength

Motivate & Inspire To Overcome

Aspire 2 Inspire

I Won’t Be Denied

Dare 2 B Diff

Instead Of “Staring” Let’s Teach “Say Hi”


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