Keep symptoms, lab results, treatments, crashes, questions, and doctor visit notes together so you do not have to rebuild your story from memory.
Built with mitochondrial disease in mind, for patients and caregivers. Come to your next visit with dates, changes, and questions in front of you, so you have less to remember under pressure.
Research and external sharing start on and can include identifiable health information. You can turn them off in Profile Settings. Read what is saved, who can access it, and your data controls.
Explore the chronic illness symptom tracker
Free organizes what you recorded. Plus adds a modeled symptom view to help prepare questions, with its limits explained.
Read the complete Free example beside the Plus report →Free tools · no account needed
Explore a treatment question, organize a discussion plan, or record a repeatable function check. You can use these tools without an account.
Explore therapies and clinical trials that may fit your priorities, then bring the possibilities to a clinician or study team.
Explore possible matches → Discussion planningOrganize supplements and interventions into a clearer, safer discussion plan instead of juggling a scattered list.
Build a discussion plan → Measuring changeCombine practical function checks into a repeatable measure so changes over time are easier to see and explain.
Measure your function →Your record should be useful before your next appointment and between visits. Choose one simple plan for the tools you need.
For patients and caregivers who want one record for day-to-day changes and visit prep. Save your health details, earlier versions of your map, and results from past function checks. Import lab and genetic PDFs and use supported wearable connections for free. The full intervention library, basic report, public tools, and research dashboards are included.
Create a Free accountFor people who want to revisit symptom and intervention questions as their health record changes. See which symptoms the model flags for discussion, explore intervention reports, and filter options by budget and time. These are modeled examples to help prepare questions, not clinical predictions.
See a sample Plus report · no signupPrices in USD. Plus renews at your chosen interval until canceled. Plus is software for organizing your health record; personal care navigation is not included.
New to Mito Map? Start with a Free appointment summary, follow the fictional founder demonstration, or review your data controls.
Represent a foundation, patient organization, or specialty practice? Ask about sponsoring Plus access for a defined group.
Choosing a way to keep track? Compare Mito Map with Bearable, Guava, or a paper symptom journal.
Explore the tracking pages, functional measurement protocols, and example reports available today. These describe the product, not its number of users or clinical effectiveness.
Mito Map is still growing. We will add patient stories only with permission and a clear account of what someone actually used; the fictional examples above are demonstrations.
Start with one symptom, one lab, or one question. Over time, Mito Map helps you build a clearer picture of what has been going on.
Review trends, patterns, and summaries you can use to prepare for appointments and decide what to track next.
Keep symptoms, sleep, activity, treatments, crashes, and lab results in order so the story is easier to explain later.
If you are interested, Mito Map can help you see research studies that may be relevant. You can ignore this if you only want personal tracking.
Turn your saved symptoms, labs, treatments, and questions into a dated summary. Bring the same summary to your next specialist or refer to it when filling in appointment and referral paperwork, so you have less to piece together again.
Follow active studies and programs preparing for patient trials. Enter a gene, variant, or syndrome in the matcher to see which options may be relevant to discuss with a study team.
A POLG activator in Phase 1 testing with healthy volunteers. Pretzel has described a POLG and mitochondrial DNA depletion syndrome patient program planned for the second half of 2026.
A Phase 2 study of KL1333 for qualifying adults with mtDNA-related primary mitochondrial disease. Recruiting availability varies by site.
A Phase 3 study for qualifying adults with a genetically confirmed mitochondrial m.3243A>G variant. Recruiting availability varies by site.
An upcoming Phase 1 basket study for qualifying participants with MELAS or LHON-Plus. Sites and enrollment timing must be confirmed with the study team.
Development status is not proof of eligibility or benefit. Study status, sites, and criteria can change. A sponsor or study team must confirm whether a patient study is open and whether someone qualifies.
Some people use Mito Map to prepare for appointments. Some use it to remember medication changes. Some use it to look for patterns. You can start wherever you are.
Save symptoms, labs, treatments, notes, and changes as they happen.
Start a patient profile Apply for a Patient SpotlightKeep updates, questions, and visit notes together when you are helping with care. Review the details together before an appointment.
Start FreeReview organized symptoms, labs, function changes, and questions before the visit gets crowded.
See clinician workflowUse organized histories, validation protocols, and research surfaces to reason from lived timelines.
Explore research toolsConnect patients to free tracking tools or ask about sponsoring Plus access for your community.
Ask about sponsored access See organization mapYou do not have to do everything at once. Add a little now, add more later, and Mito Map becomes a clearer record of your health.
Start with symptoms, diagnoses, labs, treatments, or questions.
Add crashes, recovery, new labs, medicine changes, or notes from appointments.
Review what changed, what helped, what made things worse, and what to ask next.
Use your saved information to make a clearer summary for your doctor or caregiver.
Choose what to save and review how your information is used. Research and external sharing start on, and you can turn that permission off in Profile Settings.
By default, Mito Map may use and share identifiable health information externally for research, product improvement, partnerships, and other purposes described in the Privacy Policy. Turning this permission off does not remove account access or current product features.
Read the current privacy policyYou can start with a symptom or a diagnosis. Choose a group below, then add the details that matter to you. Each path uses the same Mito Map record.
Keep activity, next-day symptoms, rest, and recovery together.
Start with fatigue →Record changes even when one diagnosis does not explain the whole picture.
Start with brain fog →Organize symptoms across body systems, existing labs, treatments, and care questions.
Start with mitochondrial disease →Keep repeat measures and notes alongside medication or life-stage changes.
Start with daily capacity →You can start with just a few details. Add more later when you have time or when something changes.
Sign up so your notes, updates, and reports stay together and are there when you come back.
Add symptoms, lab results, treatments, crashes, questions, and changes you notice.
Come back before appointments, after crashes, or when something changes so your record stays useful.
Mito Map is not another place to dump health data. It is a practical way to keep the details you actually need for daily life and doctor visits.
Save symptoms, labs, treatments, daily energy, and questions while they are fresh.
Look back at what changed around sleep, activity, food, treatments, labs, and crashes.
Turn scattered updates into a short summary and a better list of questions.
Keep track of treatments, routines, flares, and results so fewer details get lost.
Mito Map is not clinical advice. It is a careful structure for organizing lived experience, repeat measures, research context, and care questions so the next conversation starts with a better record.
Mito Map is for people who need a clearer way to track health changes and explain them to doctors, caregivers, or family.
Keep your symptoms, labs, and questions together so it is easier to explain what is happening.
Store updates and prepare visits when you are helping someone else manage care.
Look back over time so you can explain what you feel, what helps, and what makes things worse.
Organized notes can help care conversations start faster and stay focused on next steps.
Create an account and begin with the detail that matters most today. You can add more whenever you are ready.