跳到内容
  • English
  • Bahasa
  • 中文
  • தமிழ்
rare disease malaysia
  • 简介
  • 挑战与建议扩张
    • 缺乏确认和包容性
    • 缺乏意识和全面的医疗保健
    • 缺乏获得药物的途径
    • 罕见疾病患者的个人权利和尊严缺乏保护
    • 建议
  • 罕见疾病患者的维护者
  • 致敬
  • 联系
rare disease malaysia

联系

Siva SK

(Father of Swathi – Infantile Pompe Warrior) & Rare Disease Advocate

  • 6012-467 RARE (7273)
  • 6012-368 4548
  • [email protected]
  • info@localhost
rare disease malaysia

Malaysia Rare Disease communities, especially the children’s, has been embroiled with many day to day challenges for a long time. This website highlights the challenges faced by them, recommended solutions, tribute to Malaysia Rare Disease warriors / heroes, recognition to Malaysia Rare Disease champions, as well collection of media coverage on Malaysia Rare Disease. Ultimately, we desire to bring together NGO’s, government officials, medical professionals, corporates, policy makers, and citizens of Malaysia as one entity to help Malaysia Rare Disease communities, especially the children’s, in best interest of their future so they too could lead near normal life like any other child in Malaysia.

Menu

  • 马来西亚罕见病
  • 简介
  • 挑战与建议
  • 罕见疾病患者的维护者
  • 致敬
  • 联系

CONNECT

  • WhatsApp
  • Mail

Inborn Errors of Metabolism – A Survival Guide

16 7 月, 2024
rarediseasemalaysia

Rare disease in Malaysia: Challenges and solutions

5 9 月, 2020
rarediseasemalaysia

Care of people with rare diseases should not be compromised in the time of Covid-19

5 9 月, 2020
rarediseasemalaysia

Caution for rare disease patients

5 9 月, 2020
Aisha (in wheelchair) is more attached to her father Azhar (left), who showers her with affection

Parents are pillars of strength for these rare disease patients

5 9 月, 2020

© 2024 Rare Disease Malaysia | All Right’s Reserved | CSR by Ulement

1445
  • 简介
  • 挑战与建议
    • 缺乏确认和包容性
    • 缺乏意识和全面的医疗保健
    • 缺乏获得药物的途径
    • 罕见疾病患者的个人权利和尊严缺乏保护
    • 建议
  • 罕见疾病患者的维护者
  • 致敬
  • 联系