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Brief Report

Thalime: A Mobile App Designed Just for Patients and Their Families

by
Hatley Forrest McMicking
Product Growth Manager, Curatio Networks, Inc., Georgia
Thalass. Rep. 2018, 8(1), 7496; https://doi.org/10.4081/thal.2018.7496
Submission received: 10 April 2018 / Revised: 10 April 2018 / Accepted: 10 April 2018 / Published: 18 April 2018

Abstract

Introducing the first mobile app designed specifically for the Thalassemia community; Thalime, your personalized private community. Thalime is a free app that connects patients and caregivers of Thalassemia to others who know what you’re going through. Learn about your condition from a trusted source. Improve your well-being with health-tracking tools. Get support from others just like you. With personalized disease management tools designed to make life easier every day, Thalime is your all-in-one health resource that empowers you to be in control of your health. Build your private peer community to learn, share and receive support. Follow programs and set goals with our personalized recommendations and virtual coaching. Track your progress with our visual health tracker for blood transfusions and medication tracker. Additional health tracker tools allow you to monitor and share your mood, energy, pain and more.
Keywords: thalassemia; hemoglobinopathies thalassemia; hemoglobinopathies

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MDPI and ACS Style

McMicking, H.F. Thalime: A Mobile App Designed Just for Patients and Their Families. Thalass. Rep. 2018, 8, 7496. https://doi.org/10.4081/thal.2018.7496

AMA Style

McMicking HF. Thalime: A Mobile App Designed Just for Patients and Their Families. Thalassemia Reports. 2018; 8(1):7496. https://doi.org/10.4081/thal.2018.7496

Chicago/Turabian Style

McMicking, Hatley Forrest. 2018. "Thalime: A Mobile App Designed Just for Patients and Their Families" Thalassemia Reports 8, no. 1: 7496. https://doi.org/10.4081/thal.2018.7496

APA Style

McMicking, H. F. (2018). Thalime: A Mobile App Designed Just for Patients and Their Families. Thalassemia Reports, 8(1), 7496. https://doi.org/10.4081/thal.2018.7496

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