Zane RareMe Aikin Manyanci: Manhajar Wayar Hannu daga Cong Fang, Shijian Luo and Jingzhao Pan mai nasara ne mai daraja sosai na 2021 Kyautar A' Design Award ta Tagulla a Rukunin Gasar Wayar Hannu.
TagullaWayar Hannu· 2021
RareMe Aikin Manyanci: Manhajar Wayar Hannu
daga Cong Fang, Shijian Luo and Jingzhao Pan
Abokin Ciniki: Zhejiang University
Mai Nasarar Kyautar A' Design Award ta Tagulla a Rukunin Wayar Hannu
Mai Nasara da Aka Tabbatar
Tabbatar da Matsayin Kyauta na #111937Ƙirar
Game da RareMe Aikin Manyanci: Manhajar Wayar Hannu
Rubutun Littafi: RareMe wata manhajar wayar hannu ce da aka kera domin mutanen da cututtuka masu wuyar samu suka shafa. RareMe tana haɗa marasa lafiya da iyalansu da asibitoci, cibiyoyin kiwon lafiya, kantunan magani, likitoci da masu kirkirar magunguna. Masu amfani suna zaɓar matsayinsu a matsayin mara lafiya, ɗan uwan mara lafiya, ko mai bada kula ta lafiya a lokacin rijista. Marasa lafiya na iya rubuta bayanan kwanaki game da jinyarsu, su nemi magunguna da hanyoyin jinya a duk faɗin duniya, kuma su sami wasu masu amfani da ke da irin wannan yanayin ta hanyar algorithm na shawarwari. Ana samun manhajar a kan iOS da Android. Manufar ita ce a ba da hankali da kulawa daidai ga marasa lafiyar da cututtuka masu wuyar samu suka shafa.
Amincewa
Game da Kyautar A' Design Award ta Tagulla
Zanen RareMe Aikin Manyanci: Manhajar Wayar Hannu ya lashe Kyautar A' Design Award ta Tagulla, wata karramawa mai tsananin daraja da ake bai wa zane-zane na musamman waɗanda ke da ƙirƙira, basira da hikima. Waɗanda suka lashe kyautar Tagulla kayayyakin fasaha ne masu ƙwarewa da ƙirƙira mai ban mamaki waɗanda ke tabbatar da babban gogewa, tunani da dabarun masu zanensu. Ana sa ran zanen RareMe Aikin Manyanci: Manhajar Wayar Hannu ya zama abu da ake girmamawa sosai, ake sha'awa da ƙauna, mai ƙwarewa da ƙirƙire-ƙirƙire. Wannan zane da ya lashe Kyautar A' Design Award ta Tagulla yana haɗa mafi kyawun ayyuka a fasaha, kimiyya, zane da fasahar zamani, kuma yana da kyau saboda kulawarsa ga cikakkun bayanai. Zanen RareMe Aikin Manyanci: Manhajar Wayar Hannu yana biyan buƙatu da kyau, yana taɓa sha'awa, yana jan hankalin zukata kuma yana jawo sha'awar sani.
Bayan Ƙirar
Kayan Manema Labarai
Bayanin ƙungiyar, membobinta da cikakkun bayanai na fasaha da mai ƙirar ya bayar.
- Siffofi Na Musamman
- 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.
- Girma da Fakitin
- Launched on IOS and Android
- Kalmomin Alama
- Rare Disease, app, patients, crowd-funding, mutual aid
- Fasahar Samarwa
- 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.
- Ƙalubalen Zane
- 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. - Bincike
- 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. - Wahayi
- 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.
- Tsawon Lokacin Aikin
- This project started in September 2019 in Hangzhou, China, and it is still under developing.
- Tsarin Aiki
- 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.
- Mambobin Ƙungiya
- Cong Fang
Shijian Luo
Jingzhao Pan
Tianhe Zhang
Huan Lin - Godiyar Hotuna
- 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
Tallafi
Bincika Bayan Designers.org
Gano kayayyaki, ayyuka da damammaki daga abokan tallafin mu.
Ƙarin Abubuwan Bincike
Ƙirare Masu Alaƙa
Bincika ƙarin ƙirare masu lashe kyauta daga wannan rukunin, waɗanda aka zaɓa bisa cancanta.