Raremark

0:02:11

Raremark Foundation: #30in30 Campaign Launch

0:06:32

Steven Byamugisha, Co-Founder and Team lead,Raremark Foundation | NBS Impact Uganda

0:33:10

Sick Conversations: Season #2, Part 5: Life Beyond Discovering Your Genotype.

0:01:30

Raremark | Rare disease community

3:46:29

RAREMARK FOUNDATION: SHINING STAR GALA

4:09:38

ANNUAL FUNDRAISING DINNER

0:01:22

Raremark Foundation: #30in30 Campaign

0:01:19

Raremark: Make your experience count

1:23:06

#SickConversations Season #2, Part 1: A chat with Papa Okurut

1:01:50

#SickConversations: Season #2, Part 2: Advocating for Sickle Cell Warriors In The Different Spaces.

0:01:47

Julie Walters founder of Raremark

0:01:59

RareHope through Raremark on #RareDiseaseDay 2019!

0:02:48

Julie Walters of Raremark: High50 Entrepreneur

0:44:42

Sick Conversations: Season #2, Part 3: A Caregiver's Experience.

0:03:54

Digital advertising for clinical trials - Raremark

0:00:31

The Ntinda Sickle Cell Screening mission. Hosted by RareMark Foundation.

0:04:26

Interview with Raremark : My Adrenomyeloneuropathy (AMN) Experience

0:00:16

Very interesting episode of the #SickConversations up on the @Raremark.Foundation page

0:14:45

MY FIRST RARE MARK SHINY POKEMON?!

0:00:30

So I found a Rare Mark Flygon..

0:00:29

Finding a SHINY POKEMON everyday until i get one with the RAREMARK! DAY 4 #shinyhunting #Raremark

0:02:53

Sickle Cell Screening at Next Media Park, Kampala. Funded by Rare Mark Foundation, Hosted by nbs.

0:00:30

Shiny Finizen with Rare Mark encounter! (Pokémon Scarlet)

0:00:24

Finding a SHINY POKEMON everyday until i get one with the RAREMARK! DAY 5 #shinyhunting #Raremark