Ali Kimara Rare Disease Foundation

Parents and caregivers of children living with or facing significant health challenges that hinder their ability to attend school, let's not deny them their right to education. Currently, education is reaching them at home through the official guidelines launched by the Ministry of Education, Science and Technology.

Rare Diseases International
Rare Disease Day

SIKU YA MAGONJWA ADIMU DUNIANI 2024

🚨 IT'S OFFICIALLY RARE DISEASE DAY ACROSS THE GLOBE 🚨

Join us in marking Rare Disease Day 2024 now that it's finally here! Let's unite in solidarity with the millions worldwide living with rare diseases. 🌍 Spread awareness, share stories, and show support for them.

Together, we can make a lasting impact and shine a light on these often overlooked!

Let's make today count by raising awareness and advocating for those who need it most. Every voice matters in the fight for understanding and support.

Visit our website to find out more:https://www.rarediseaseday.org/

Siku ya Magonjwa Adimu Duniani mwaka huu itaadhimishwa Tarehe 29, Februari.Moja ya mtu mwenye magonjwa Adimu ni Ali Kimara, Mtoto ambaye amejaaliwa talanta mbalimbali na anazionesha kupitia ufaulu wake kupitia mfumo wa Elimu nje ya Shule. Ali ana ndoto za kuwa Rubani. TUMUOMBEE.
Ali Kimara Rare Disease Foundation
Rare Disease Day
Zanzibar Human Genetics Zhgo

Ali Kimara Rare Disease Foundation & Muhimbili University of Health and Allied Sciences unite for impactful research to unlock hope for those facing rare diseases.

Siku ya magonjwa adimu duniani itaadhimishwa tarehe 29 Februari 2024.

Taasisi za Ali Kimara Rare Disease Foundation na Muhimbili University of Health and Allied Sciences zinaungana katika kampeni ya kuchochea tafiti zitakazosaidia kuwatambua waathirika wa magonjwa haya nchini.




Rare Disease Day
Rare Diseases International
Wizara ya Afya

Meet Dr Mohamedraza A Ebrahim

Meet Dr Mohamedraza Ebrahim

Date: Friday 16 February
Time: 13h30 – 13h45
Topic: The role of patient organisation’s in gaining access for patients in Africa
Session: Breakaway – Policy

Mohamedraza Ebrahim, a dedicated paediatrician in Tanzania, extends his compassionate care to children, including those battling rare diseases, despite the constraints of limited resources. His commitment to children's well-being drives him to search for innovative solutions to the unique challenges they face. Dr. Ebrahim's professional journey finds him at The Aga Khan Hospital in Dar es Salaam, Tanzania, where he also holds a senior instructor position at The Aga Khan Hospital, Dar Es Salaam. Graduating from Stellenbosch University in Cape Town, South Africa, he returned to Tanzania with invaluable skills and experience gained abroad to focus on capacity building and teaching in his homeland. Collaborating with the Ali Kimara Rare Disease Foundation, he continues to educate on rare diseases, understanding the vital role of awareness. Dr. Ebrahim shares his expertise as an instructor for Basic Life Support, Paediatric Advanced Life Support, and Paediatric Emergency Assessment, Recognition, and Stabilization (PEARS).

Head over to www.rare-x.co.za to have a look at our full programme of speakers and all things Rare-X.

-x

Uzinduzi wa miongozo ya elimu maalumu na Jumuishi Asante sana kwa hili tunathamini sana hatua hizi kubwa

Mungu ibariki Tanzania

.kimara

Uzinduzi wa miongozo 4 ya kuboresha utoaji elimu kwa wanafunzi wenye mahitaji maalum.
Unaofanyika 12.9.2023 Dodoma katika ukumbi wa Destination kisasa. Mgeni rasmi ni Waziri wa Elimu, Sayansi na Teknolojia.

Miongozo hiyo ni
1. Home schooling (Shule Nyumbani)
2. Home visit (Ziara Nyumbani)
3. Ubainishaji na upimaji wanafunzi wenye mahitaji maalum
4. Uanzishwaji na usimamizi wa shule au vyuo maalum/ jumuishi

.kimara

"Leave no one behind!" ni ahadi ya waishio na kuwa hakuna atakaeachwa! Hivyo basi na Ali nae hakuachwa, yeye na sis wake wote ni mwendo wa kuchomekea.