Sickle Cell Support Foundation of Jamaica

Sickle Cell Support Foundation of Jamaica "We support families affected by Sickle Cell Disease and advocate for greater awareness, care, and resources. This was achieved in June 2015.

Our mission is to empower warriors, educate the public, and strengthen the fight against Sickle Cell in Jamaica." The Sickle Cell Support Foundation of Jamaica (SCSCJ) is a non-profit, registered charitable organisation founded in October 1992, by two sickle cell patients, Camille Daley and Morette Wright. Our mission is to provide support (social, emotional and material) to patients and their families and to share coping strategies which will enable them to live healthier, more meaningful lives. We also seek to heighten public awareness of sickle cell disorders (SCD) and dispel the many myths and misconceptions surrounding them. Each year we hold annual Sickle Cell Awareness Weeks and have produced an educational Get the Facts on Sickle Cell brochure and a Teachers' Guide to Sickle Cell Disease. We are an advocate for persons with sickle cell disorders and lobbied government in 1993 to restart newborn screening of babies in Jamaica. We also successfully lobbied along with the Sickle Cell Unit, UWI to have SCD added to list of illnesses supported by the National Health Fund. We seek remove the stigma attached to the disease which causes many persons to hide the condition for fear of discrimination. Ultimately we wish to create an enabling environment within which individuals with sickle cell disease can flourish and realize their true potential. We also assist persons who have not been able to complete school because of their illness and need remedial education, skills training, assistance with medication and medical procedures/tests and with funds to start or expand a small business. We need more members/volunteers to help us achieve these goals.

✨ Our First Empowerment Session for 2026 is Here! ✨The Sickle Cell Support Foundation of Jamaica warmly invites all warr...
22/01/2026

✨ Our First Empowerment Session for 2026 is Here! ✨

The Sickle Cell Support Foundation of Jamaica warmly invites all warriors, caregivers, and supporters to our Monthly Virtual Empowerment Meeting as we kick off the new year strong.

🧠 Theme: Start Strong: Reset Your Mind, Routine & Resilience

Join us for an empowering and insightful session with Ms. Sosheina Whyte, Associate Counselling Psychologist, as we focus on mental wellness, resilience, and practical strategies to help you move forward with purpose in 2026.

📅 Thursday, January 29, 2026
⏰ 7:00 PM
📍 Zoom

Let’s begin the year grounded, encouraged, and empowered together. ❤️💪🏽

💪🏽❤️‍

We’re Back for 2026! The Sickle Cell Support Foundation of Jamaica proudly presents our 2026 Monthly Empowerment Meeting...
22/01/2026

We’re Back for 2026!

The Sickle Cell Support Foundation of Jamaica proudly presents our 2026 Monthly Empowerment Meeting Series:

RISE 2026: Stronger Minds, Healthier Lives!

Join us monthly on Zoom as we focus on wellness, resilience, education, and advocacy for persons living with sickle cell disease, parents/caregivers, supporters, and advocates.

Each session will provide:
• practical education from qualified guest speakers
• interactive discussion and Q&A
• “Sharing & Caring” support and connection
• tools to strengthen wellness, resilience, and self-advocacy

Let’s build strength together — one session at a time.

Meeting Topic and Zoom details will be shared monthly.

12/01/2026

GoFundMe link in Story.

❤️💞❤️ ❤️💪🏾💪🏾

We are supporting Mishcah on her journey toward healing through a needed hip replacement. Every contribution makes a dif...
12/01/2026

We are supporting Mishcah on her journey toward healing through a needed hip replacement. Every contribution makes a difference, and if you’re unable to donate, sharing this post is a powerful way to help. Thank you for standing with her. 💙

From a fellow warrior:If You’re Battling a Stubborn Leg Ulcer, Please Read This 👇👇I’m making this post because I’ve seen...
12/01/2026

From a fellow warrior:

If You’re Battling a Stubborn Leg Ulcer, Please Read This 👇👇

I’m making this post because I’ve seen so many messages and questions in my DM about what can actually help heal leg ulcers.

So many warriors don’t even know what leg ulcers are. While some are battling ulcers that have lasted for months, even years.

That’s why they’re often called stubborn ulcers.

During my own leg ulcer treatment, there was something my doctors used as part of my care that I don’t see people talk about much in this space, but it really helped me.

💡 ELASTOPLAST BANDAGES

Here’s how elastoplast bandages help with leg ulcers 👇

🩹 Provides firm but gentle compression:
Elastoplast bandages apply steady pressure around the leg, which helps improve blood circulation. Better blood flow means more oxygen and nutrients get to the wound to support healing.

🩹 Reduces swelling around the ulcer:
Swelling slows down healing. Compression helps reduce fluid buildup around the wound, making it easier for the ulcer to close.

🩹 Keeps the wound protected and stable:
It holds dressings firmly in place and protects the ulcer from friction, dirt, and repeated injury, which is very important for warriors.

🩹 Supports the leg while walking:
For warriors who still need to move around, elastoplast gives support to the leg and reduces strain on the wound area.

Please note: Elastoplast bandages should be applied by a trained health worker or under medical guidance. Wrong application can worsen circulation instead of helping.

And yes! Leg ulcers are not spiritual. They are medical.
They need patience, consistency, proper wound care, good nutrition, hydration, and professional medical support.

If you or someone you love is battling a leg ulcer, please don’t give up. Healing is possible, even when it takes time.🥰🫶

👉 Share this post. It might help someone who has been suffering quietly.

Dear Warrior,You are not a burden. You never have been, and you never will be.As someone living with sickle cell and wor...
12/01/2026

Dear Warrior,

You are not a burden. You never have been, and you never will be.

As someone living with sickle cell and working as a genetic counsellor, I speak from both lived experience and professional understanding.

Sickle cell is a condition, not a definition. It is something you manage, not something that diminishes your worth.
The fact that your journey sometimes includes pain, hospital visits, or moments of vulnerability does not make you a burden.

It makes you HUMAN.

Many warriors grow up feeling they have to apologise for being unwell, for needing rest, for asking for support, or for changing plans.
Over time, that quiet apology can turn inward and become self-blame.
I want to gently remind you that needing help is not a failure. It is a natural part of living with a long-term condition, just as glasses are part of living with poor eyesight or insulin is part of living with diabetes.

Your life has value beyond sickle cell disorder. Your worth is not measured by how much you can endure in silence, how rarely you ask for help, or how well you hide your pain. You matter simply because you exist. Your presence enriches families, friendships, workplaces, and communities in ways that are often unseen but deeply felt.

As a genetic counsellor, I have seen how much resilience lives within the sickle cell community. As a warrior, I know that resilience does not mean being strong every day. It means allowing yourself grace on the hard days and recognising that rest, boundaries, and care are acts of strength.

So please remember this.
You are allowed to take up space.
You are allowed to need care.
You are allowed to live fully, loudly, and honestly. You are not a burden.
You are a person with a story, a purpose, and a future that matters.

Be gentle with yourself.

The world is better because you are in it.

❤️💪🏾💪🏾

New Year, renewed hope. 💛 Here’s to a 2026 filled with breakthroughs and better health for our warriors. Happy New Year ...
02/01/2026

New Year, renewed hope. 💛 Here’s to a 2026 filled with breakthroughs and better health for our warriors. Happy New Year from the Sickle Cell Support Foundation of Jamaica!

Season’s Greetings from the Sickle Cell Support Foundation of Jamaica 🎄✨As we celebrate the joy of Christmas and look fo...
24/12/2025

Season’s Greetings from the Sickle Cell Support Foundation of Jamaica 🎄✨

As we celebrate the joy of Christmas and look forward to a hopeful New Year, we extend warm wishes to all our warriors, caregivers, families, and supporters.

This season, we gently remind our warriors to:
Stay warm, especially during cooler nights.
Stay well hydrated.
Get enough rest and listen to your body.
Seek support whenever you need it. You are never alone.

May this holiday season bring peace, strength, comfort, and renewed hope. Here’s to a brighter, healthier New Year ahead for us all.

With love and solidarity,
Sickle Cell Support Foundation of Jamaica ❤️

❤️ 💪🏽❤️‍

17/12/2025

Our Mobile Pharmacy Units are serving communities in St. James, Westmoreland and St. Elizabeth today.

St. James:
-Maroon Town Health Centre
-Mt. Carey Health Centre

Westmoreland:
-Williamsfield Health Centre

St. Elizabeth:
-Slipe Cross Road

If you’re nearby, stop by to fill your prescriptions and access NHF services. 💙

Address

Kingston

Telephone

+18768845431

Website

Alerts

Be the first to know and let us send you an email when Sickle Cell Support Foundation of Jamaica posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram