We're teaming up to connect the
Zamplo is a platform that empowers people with the resources, knowledge, and tools they need to mobilize their personalized data.
Zamplo empowers you to manage your health journey - digitally.
Now you can privately and easily use your smartphone or tablet to...
Create a "Virtual Binder"
Create journal entries with your pompe symptoms, medications/supplements, activities, health data, notes and questions that save to your "virtual binder."
Easily take a photo with your smartphone or tablet of your health information including lab results, MRI/CT/PET scans, blood work, prescriptions and referrals and save as attachments to your "virtual binder"
Zamplo Premium uses optical character recognition, to easily search keywords through your virtual binder.
No more flipping through pages!
Ditch the physical binders and have true data portability with everything you need, where and when you need it.
Read more about the benefits of journaling throughout your health care journey.
Invite Caregivers and Careteam
Invite a caregiver
Friends and family often play a huge role in your health care journey.
Instead of passing around a binder, invite a caregiver to contribute to your virtual binder.
They too can easily scan, enter and manage your health care information.
Invite a member from your Careteam
Instead of telling your story over and over again, invite a member of your Careteam to contribute, manage and view your health care information.
You control the level of access of your Caregivers and the members of your Careteam.
Graph Your Health Data
Throughout any health journey, patients and caregivers collect overwhelming amounts of health data and information.
Using Zamplo, you can track, graph, analyze and view trends in your pompe disease symptoms, activities and health data.
Better understanding your trends in your health data, will allow for more informed decision-making and enhance your engagement at your medical appointments and throughout your health care journey.
Read more about the importance of taking control of your health care data.
Whether it's the uncertainty, the frustration of telling the same story to four different health care providers in one day, or the effects of treatment, a health journey can leave you exhausted when you need your energy the most.
Before your next appointment, create a report to summarize the information in your journal entries to provide a snapshot of your pompe disease symptoms, medications, health data, treatment regime, and questions.
Feel more organized and more empowered to advocate for yourself, by having your health data in your hands.
Read more from a patient's perspective about leading your own health journey.
We know you have a lot to remember...
Keeping track of medications, monitoring symptoms, diet and food intake, movement and exercise, and mental health check-ins can be overwhelming.
Let us help remind you!
Set up a routine by entering and creating reminders for reoccurring medications, supplements and activities while tracking health data and symptoms.
Zamplo connects to Health Canada Drug Product Database to provide accuracy with your medications and supplements.
Create a Community of Support
We understand that it can be hard to meet
or find others with the same health journey.
With the Community feature, you can connect with people worldwide who have the same or similar diagnosis.
You can chat one-to-one and compare the different health journeys someone can take while having the same diagnosis.
Find support in a global community of peers and
motivate others to take control of their health journeys.
Your conversations are encrypted and never shared.
Security and Privacy By Design
Zamplo, as a connected health platform, has been designed with security and privacy at its foundation. Regardless of your privacy-related decisions, we will ensure that our security is continuously monitored, tested and enhanced to keep your data safe.
Each user has complete control over the collection, use and disclosure of personally identifiable information. Any information that is de-identified and aggregated will only be used for research purposes, not marketing. Any identifiable information will only be collected for research with the informed consent of users.