Mitochondrial Disease — Care3 | Make Your Miracle

Care3 for Mitochondrial Disease

Finally. An App for Mitochondrial Disease

Whether you need help managing your mitochondrial disease symptoms or if you care for someone with mito, we are here for you.

Welcome to the first and only digital health platform (website and mobile app) specifically for managing life with mitochondrial disease.

Care3 will help you manage mito each day by:

“The best way to predict the future is to create it.”

-Abraham Lincoln

How Care3 for Mito Works

What you get when you join:

More than 200 people have joined Care3 to own and manage their mito health experience.

Sponsored by

MitoAction is sponsoring Care3 for people dealing with mitochondrial disease. Get FREE access through this page only.

SIGN UP FREE!

You MUST sign up via the button below to bypass the pay wall .

  1. For the best experience, sign up using your computer or iPad/Android tablet (you can sign up using your mobile phone as well).
  2. Once you see the “Mito Daily” screen below, tap “let’s go” to unlock your custom timeline FREE.
  3. Then check your email. A Welcome message has the link to download the Care3 mobile app.

Tap/click “let’s go” to unlock custom mito features

Yes! Sign me up FREE!

NOTE

Care3 is available on iPhone, Android and web. Below is a demo below of Care3 on the web.

HIPAA Compliant

Care3 is HIPAA-compliant. Your health information and chat conversations are safe and secure.

Types of Mitochondrial Diseases addressed by
Care3 for Mito

mitochondrial disease, mitochondrial syndrome, mitochondrial diseases, Carnitine Transport Defect, Primary Carnitine Deficiency, Carnitine-Acylcarnitine Translocase, CACT Deficiency, Carnitine Palmitoyl Transferase Deficiency, CPT I Deficiency, CPT II Deficiency, Very Long Chain Acyl-CoA Dehydrogenase Deficiency, VLCAD Deficiency, Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, LCHAD Deficiency, Trifunctional Protein Deficiency, TFP Deficiency, Medium Chain Acyl-CoA Dehydrogenase Deficiency, MCAD Deficiency, MCHAD/SCHAD Deficiency, MCKAT Deficiency, 2,4 Dienoyl-CoA Reductase Deficiency, Short Chain Acyl-CoA Dehydrogenase, Deficiency, SCAD Deficiency, 3-Hydroxy Acyl CoA Dehydrogenase Deficiency, HADH Deficiency, Electron Transfer Flavoprotein Dehydrogenase Deficiency, ETF Dehydrogenase Deficiency, 3-Hydroxy-3 Methylglutaryl-CoA Lyase Deficiency, HMG Deficiency, ACAD9 Deficiency, Autosomal Dominant Optic Atrophy, ADOA, Barth Syndrome, LIC, Lethal Infantile Cardiomyopathy, Carnitine Deficiency, Creatine Deficiency Syndromes, Complex I, II, III, IV, V Deficiency, Chronic Progressive External Ophthalmoplegia, CPEO, LBSL, Leukodystrophy, LCAD, Leigh Disease, Leigh Syndrome, LHON, Luft Disease, MELAS, MERRF, MIRAS, Mitochondrial Cytopathy, Mitochondrial DNA Depletion, Mitochondrial Encephalopathy, Mitochondrial Myopathy, Multiple Mitochondrial Dysfunction Syndrome, MNGIE, NARP, Pearson Syndrome, Primary Mitochondrial Myopathy, Pyruvate Carboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, PDCD, PDH, POLG2 Mutations