RareMe

App for Zhejiang University

Rare diseases (A kind of disease that few people suffer from) currently affect an estimated 300 million worldwide. Because of their rare condition, the patients can not get the same care and assistance as normal patients especially in some developing countries. This APP connects patients with rare diseases, medical research institutions, hospitals, doctors, charities, drug developers and others in the world to help patients with rare diseases recover and treat them. In the APP, patients with rare diseases can receive equal attention and care.

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RareMe by Cong Fang

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App by Cong Fang

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Cong Fang RareMe

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Cong Fang App

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Zhejiang UniversityBrand Logo

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RareMe App Press Releases

Press resources for RareMe are offered in several languages: English.

RareMe App Media Articles

For immediate use: RareMe articles, available in languages such as Portuguese, English, Spanish, French, Italian, Dutch, German, Hindi, Turkish, Arabic (Standard), Indonesian, Korean, Japanese, Russian and Chinese (Mandarin), to enrich your content.

Unique Properties

Rare diseases are currently affecting about 300 million patients worldwide. Due to their rare conditions, they cannot get the same degree of treatment and assistance as normal patients, especially in some developing countries. RareMe helps rare diseases patients with their recovery and therapy. By connecting with global medical research, institutions, hospitals, doctors, and drug developers, they can receive equal attention and care.

Tags

Rare Disease, app, patients, crowd-funding, mutual aid

Production Technology

RareMe is an APP,which connects patients and their families with health-care providers, such as hospitals, medical institutions, pharmacies, doctors, drug developers, pharmaceuticals companies, etc. It also links rare disease patients with similar conditions with medical workers through intelligent recommendation algorithm, so as to make them feel not alone.

Design Challenge

RareMe connects patients and their families with health-care providers, such as hospitals, medical institutions, pharmacies, doctors, drug developers, pharmaceuticals companies, etc. The biggest problem is to contact all stakeholders, promote app through hospitals, medical institutions, and major media platforms, so that patients scattered around the world can know and join RareMe. With the help of a large number of patients gathering to solve the problem of drug research and distribution by low-cost crowdfunding.

Project Duration

This project started in September 2019 in Hangzhou, China, and it is still under developing.

Operation Flow

At the beginning of registration, user will choose their own role as patients/family members or health-care providers, then enter the home page. Patients can write disease fighting diaries, seek for other users who have similar syndromes and fight together. They can also seek drugs and treatments around the world. As for health-care providers, they can contact patients quickly via RareMe and offer help.

Research

Rare diseases are currently affecting 3.5% - 5.9% of the worldwide population. There are more than 7,000 rare diseases known in the world, however, only less than 10% of the diseases have approved treatment drugs or programs. Based on this huge social problem, we have conducted extensive interviews with medical professors of Harvard University and Medical Laboratory of Zhejiang University, and are eager to connect rare disease patients around the world in a simple and portable way. We have connected many medical workers and patients via the development of RareMe. In order to improve this current condition, we will add in more and more health-care providers in the future.

Inspiration

Rare diseases are lately affecting 3.5% - 5.9% of the worldwide population. More than 7,000 rare diseases are known, however, only less than 10% have approved treatment cures or programs. Due to the patients’ rare conditions, they’re not able to get the same degree of care and assistance as normal patients. Moreover, proper medicines and treatments are not available in some developing countries. They have few wardmates to communicate with, either.

Image Credits

The four images used in the app design are from the SHETU website(https://699pic.com/), and have been authorized. The authorization agreement is shown in the link Link: https://pan.baidu.com/s/1-s5VTAN_XWqHc2ZyToIegQ Password：70bo

Project Overview

RareMe App has been a Bronze winner in the Mobile Technologies, Applications and Software Design award category in the year 2020 organized by the prestigious A' Design Award & Competition. The Bronze A' Design Award is given to outstanding designs that showcase a high degree of creativity and practicality. It recognizes the dedication and skill of designers who produce work that stands out for its thoughtful development and innovative use of materials and technology. These designs are acknowledged for their professional execution and potential to influence industry standards positively. Winning this award highlights the designer's ability to blend form and function effectively, offering solutions that enhance people's lives and wellbeing.

Bronze Recognition

Cong Fang was recognized with the coveted Bronze A' Design Award in 2021, a testament to excellence of their work RareMe App.

Cong Fang Press Releases

Journalists and media members can enrich their content with our press releases on Cong Fang, available for free use. Journalists can access 1 press releases immediately, ready for your use.

RareMe: Connecting Rare Disease Patients with Global Healthcare

RareMe is an innovative app designed to connect rare disease patients with global healthcare providers, offering equal attention and care.

Cong Fang Newsroom

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