The 2015 annual “Mito Town Meeting,” held on Friday, Jan. 9, 2015, was a huge success!
The annual town meeting is our way of kicking off the new year by sharing all that is planned for the next 12 months. We’ll hear from organizations, camps, and companies around the globe that have special opportunities, programs, and projects for patients and families with mitochondrial disease.
As you listen to all of these speakers, you realize that, although the day-to-day of living with this disease can be so challenging and frustrating, you’re not alone and a lot of good is being done and a lot of people are dedicating a lot of energy and passion to making it better, said Cristy Balcells, RN MSN, Executive Director of MitoAction. We’re making great strides as a community and that’s really exciting!Date: 01/10/2015
The annual town meeting kicks off the new year by sharing what we have in store for the next 12 months! We will hear from organizations around the globe with special opportunities, programs and projects for those affected by mitochondrial disease.