Swabrah can now walk without pain, full of hope & joy.
This was only possible because of your kind support. Thank you to everyone who donates and supports Raremark Foundation! 🙏🏿 Watch her story 👇🏿
🙏🏿 https://t.co/tokMsa2Rym
Swabrah's story is one of perseverance. Despite facing numerous challenges, she is now happy to walk without pain, thanks to her hip replacement surgery.
📹 https://t.co/DDDx8L8iFp
#HopeForWarriorsFund#RaremarkFoundation
“When I first discovered I had Renal Cell Carcinoma in 2022, I wondered how I would survive both Sickle Cell disease and cancer. I felt overwhelmed.” - @angellanam2010
For @angellanam2010 , life seemed to come to a standstill after that diagnosis. Balancing two serious conditions felt impossible, and for a while, fear took over. But over time, she began to find her light again in her faith, in the people who stood by her, and in her own quiet strength.
Today, she stands as a survivor, proof that even in the hardest battles, healing is possible. Her journey reminds us that strength is the courage to keep moving forward under any circumstances.
To every warrior out there, Angella’s story is proof that you can rise above every challenge and any illness that comes your way.
Start your morning with purpose! Catch our very own @steven_B256 and @angellanam2010 LIVE on NBS Breakfast Meeting as they discuss the power of collaboration in advancing sickle cell advocacy, treatment, and support systems.
🗓️ 15TH, October
⏰9AM
📍NBS TV
Tell a friend to tell a friend, you don’t want to miss this one!
🎙 Tomorrow, 9:30AM
Don’t miss @steven_B256 and @angellanam2010 as they sit with #NextRadioUg on the Next Morning Switch and unpack how collaboration drives progress in advancing sickle cell treatment, advocacy, and support systems.
A link to the @RaremarkFdn
Josephine Esisa Shining star gala 3rd edition.
Thank you to everyone that supported the mission to support and elevate the stories of Sickle cell warriors
https://t.co/inRYHMzhG5
What happens when we become intentional about Sickle Cell disease?
What if one night could remind you of why we collaborate and strive to improve the welfare of those affected by Sickle Cell disease?
#ShiningStarGala
This afternoon, catch our very own on Sanyu Fm as they unpack some of our initiatives and impact.
Also look out for what to expect at the #ShiningStarGala
"The biggest challenge I faced was transitioning from being a free girl to a girl whose movements had to be aided."
Marion’s story is one of the few that truly shows the power of resilience, but it's also a story about what we can achieve when we come together. Every milestone she has reached is a testament to collaboration and collective impact.
The #ShiningStarGala, honors the lives that have been transformed and the hearts that made it possible.
Reserve your spot today and celebrate more of these beautiful stories with us this Friday.
If you love being part of a good cause, bring your beautiful and awesome self like @joelanthony23 is. We have a spot reserved for you at our #ShiningStarGala happening this Friday.
We can't wait to see you among our shining stars.
#4DaysToGo
Betty's story is one shared and experienced by many Warriors, the struggle, transformation and resilience are just a tip of the many wonderful stories we're excited to share with you at the #ShiningStarGala25
Sickle cell disease is silently a big burden to the poor communities especially in Northern Uganda.
We can only pursue a sickle cell free-generation through holistic partnerships, advocacy and limitless awareness about this preventable sickness.
Let’s break the silence, REPOST, RETWEET AND SHARE.
💉 Advocate for screening
🩸Donate blood
🗣️ Educate your community
#SickleCellAwareness #NorthernUganda #HealthForAll #InspireMadiXSPACE
RareMark Foundation Holds Sickle Cell Awareness Drive at Vision Group
The @RaremarkFdn is currently conducting a sickle cell disease (SCD) awareness campaign at the @VisionGroup offices.
Since morning, the Foundation has been offering free sickle cell screening, on-site medical consultations, and expert education on SCD. The initiative aims to promote early diagnosis, informed care, and greater public awareness of the condition.
The campaign is part of the Foundation’s ongoing efforts to combat sickle cell disease across Uganda.
Photos by Miriam Namutebi ||
As we kick off this week. I wanted to shine a light on a very important milestone.
Last Friday, @RaremarkFdn signed an MOU with Bethlehem Healthcare in Kyotera! We’re teaming up to help more sickle cell warriors in the community & across Uganda.
Worried about the EPS cameras?
There’s an app for that!
Download @waze. Guys have already mapped out where EPS cameras and police men are.
Join, the more the merrier.
Share the word, help a driver.
Thanks @steven_B256
Today, we partnered with @RaremarkFdn & Nakasero Blood Bank to host a successful Sickle Cell Awareness & Testing Drive & support blood donation efforts.
Our colleagues from @simbatelecom & @SkyzHotel joined us to learn about sickle cell disease, undergo on-site testing & donate blood.
We extend our heartfelt appreciation to the Foundation for their valuable partnership & the Nakasero Blood Bank for facilitating the blood donations.
A big thank you to all Simba Group employees & guests who participated — your contribution is making a real difference and helping us all become better informed.
@RaremarkFdn@busbyallan Huge thanks to the incredible doctors at Bethlehem Hospital for the incredible work they are doing for the community and warriors. We look forward to changing even more lives together. 💙 #HopeForWarriors