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 dy by:
helping you access and view past health history on demand
making it easy to track current mito symptoms and treatments to see what works and what doesn’t
helping you manage future appointments and tasks, to avoid obstacles and triggers
“The best way to predict the future is to create it.”
-Abraham Lincoln
How Care3 for Mito Works
What you get when you join:
Your Health Journal Timeline to add all of your past health history files, like past lab results, so you can access them anytime.
Your “Mito Daily” reminders to track your current mito symptoms, recommended by top thought leaders in mitochondrial disease research.
Real-time charts so you know what is working and what isn’t. Share these charts with your doctors so they see your mito experience.
A calendar to coordinate future activities, tasks, appointments, and medications so all care gets delivered, nothing falls through the cracks, and others can help you when needed.
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.
For the best experience, sign up using your computer or iPad/Android tablet (you can sign up using your mobile phone as well).
Once you see the “Mito Daily” screen below, tap “let’s go” to unlock your custom timeline FREE.
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
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 is 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