RareMe Mobilā lietotne — Cong Fang, Shijian Luo and Jingzhao Pan

Darbs RareMe Mobilā lietotne, kura autors ir Cong Fang, Shijian Luo and Jingzhao Pan, ir augsti novērtēts un ļoti prestižās 2021 Bronzas balva A' Design Award ieguvējs kategorijā Mobilo tehnoloģiju, lietotņu un programmatūras dizains.

BronzasMobilais· 2021

RareMe Mobilā lietotne

Autors: Cong Fang, Shijian Luo and Jingzhao Pan

Klients: Zhejiang University

Bronzas balva A' Design Award ieguvējs kategorijā Mobilais

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Krāsas

Dizains

Par RareMe Mobilā lietotne

RareMe ir mobilā lietotne cilvēkiem, kurus skārušas retas slimības. RareMe savieno pacientus un viņu ģimenes ar slimnīcām, medicīnas iestādēm, aptiekām, ārstiem un zāļu izstrādātājiem. Reģistrācijas laikā lietotāji izvēlas lomu — pacients, ģimenes loceklis vai veselības aprūpes sniedzējs. Pacienti var rakstīt dienasgrāmatas par savu ārstēšanu, meklēt medikamentus un ārstēšanas metodes visā pasaulē, kā arī atrast citus lietotājus ar līdzīgiem veselības stāvokļiem, izmantojot ieteikumu algoritmu. Lietotne ir pieejama iOS un Android platformās. Mērķis ir nodrošināt retu slimību pacientiem vienlīdzīgu uzmanību un aprūpi.

Atzinība

Par Bronzas balva A' Design Award

RareMe Mobilā lietotne ir Bronzas balvas A' Design Award ieguvējs, ļoti prestiža atzinība, ko piešķir izciliem dizainiem, kas izceļas ar radošumu, atjautību un viedumu. Bronzas ieguvēji ir pietiekami prasmīgi un pārsteidzoši radoši darbi, kas apliecina to dizaineru plašo pieredzi, iztēli un izdarību. Sagaidāms, ka RareMe Mobilā lietotne būs augsti vērtēts, apbrīnots un cienīts priekšmets, ievērojami profesionāls un inovatīvs. Šis ar Bronzas balvu apbalvotais dizains iekļauj labāko praksi mākslā, zinātnē, dizainā un tehnoloģijās un izceļas ar uzmanību detaļām. RareMe Mobilā lietotne lieliski apmierina vajadzības, skar vēlmes, valdzina jūtas un piesaista zinātkāri.

Aiz dizaina

Preses materiāli

Dizainera sniegtie autori, komandas dalībnieki un tehniskie dati.

Unikālās īpašības: 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.
Izmēri un iepakojums: Launched on IOS and Android
Birkas: Rare Disease, app, patients, crowd-funding, mutual aid
Ražošanas tehnoloģija: 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.
Dizaina izaicinājums: 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.
Pētījums: 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.
Iedvesma: 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.
Projekta ilgums: This project started in September 2019 in Hangzhou, China, and it is still under developing.
Darbības plūsma: 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.
Komandas dalībnieki: Cong Fang
Shijian Luo
Jingzhao Pan
Tianhe Zhang
Huan Lin
Attēlu autori: 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