Volunteer for Mito411

Name
First Last
Email*
Phone
What is your connection to mito?*
What interests you in becoming a Mito411 Volunteer?*

Monthly Expert Series

Gain knowledge from our guest speakers on topics important to the mitochondrial disease community.

MitoAction Mobile

Manage your day-to-day with mito, track symptoms, medications, and collaborate with your care team.

Mito411 Support

Receive one-on-one support from those who understand your journey with mitochondrial disease.

P.O. Box 310

Novi, MI 48376

888-648-6228

info@mitoaction.org

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Name*
First Last
Email*
Address
Street Address City State ZIP Code
Phone
What is your connection to mito?
- Patient
- Parent
- Spouse
- Caregiver
- Son
- Daughter
- Sibling
- Grandparent
- Grandchild
- Aunt
- Uncle
- Cousin
- Niece
- Nephew
- Friend
- Teacher/Educator
- Medical Professional
- Physician
- Nurse
- Genetic Counselor
- Social Worker
- Researcher
- Industry Rep
- Other
What is your or your child's diagnosis?
- Alper's Disease
- Autosomal Dominante Optic Atrophy (ADOA)
- Barth Syndrome
- Beta-Oxidation Defects
- Carnitine Deficiency
- Chronic Progressive External Ophthalmoplegia (CPEO)
- Complex I Deficiency
- Complex II Deficiency
- Complex III Deficiency
- Complex IV Deficiency
- Complex V Deficiency
- CoQ10 Deficiency
- CPT I Deficiency
- CPT II Deficiency
- Creatine Deficiency Syndrome
- Fatty Acid Oxidation Disorders (FAOD)
- Friedreich's Ataxia
- Kearns-Sayre Syndrome (KSS)
- Lactic Acidosis
- LCAD
- LCHAD
- Leigh's Disease
- Leukodystrophy
- LHON
- LHON Plus
- Luft Disease
- MCAD
- MELAS
- MEPAN
- MERRF
- MIRAS
- Mitochondrial Cytophy
- Mitochondrial DNA Depletion
- Mitochondrial Encencephalopathy
- Mitochondrial Myopathy
- MNGIE
- Multiple Acyl-CoA Dehydrogenase Deficiency (MAD)
- Multiple Mitochondrial Dysfunction Syndrome
- NARP
- Pearson Syndrome
- POLG Mutations
- Primary Mitochondrial Myopathy
- Pyruvate Carboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- Pyruvate Dhydrogenase Complex Deficiency (PDCD)
- SCAD
- SCHAD
- Thymidine Kinase 2 Deficiency (TK2)
- VLCAD
- Undiagnosed
- Other
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