Rare Disease Fund

Rare Disease Fund A charity fund for patients with rare diseases who need costly medicines for life.

It's the word that keeps rare disease families up at night — not "can we afford this now," but "can we afford this forev...
19/08/2026

It's the word that keeps rare disease families up at night — not "can we afford this now," but "can we afford this forever." A monthly gift, however small, helps answer that. ♾️

To donate, go to giving.sg/rare-disease-fund

For most people, dinner with family is part of the day. For someone living with a rare disease 🧬, just being present aft...
18/08/2026

For most people, dinner with family is part of the day. For someone living with a rare disease 🧬, just being present after a full day of appointments can mean everything.

🌟 Help make moments like this possible for more families. Donate today.
giving.sg/rare-disease-fund

This week's word is one of our favourites, because every dollar you give to RDF doesn't just help once; the government t...
12/08/2026

This week's word is one of our favourites, because every dollar you give to RDF doesn't just help once; the government triples it. Small gifts, quietly multiplied. 💰

To learn more, go to kkh.com.sg/giving/rare-disease-fund 💫

Happy National Day! 🇸🇬This year, let's go beyond a share or a like into support that truly carries a family through trea...
09/08/2026

Happy National Day! 🇸🇬

This year, let's go beyond a share or a like into support that truly carries a family through treatment. 🩵

Awareness is where it starts. But rare disease families need more than understanding; they need us alongside them for the long road ahead. 🛣️🧬

Give Hope for a Lifetime: giving.sg/rare-disease-fund

It can take years just to get a diagnosis. Then comes the real shock treatment that can cost more than most families ear...
07/08/2026

It can take years just to get a diagnosis. Then comes the real shock treatment that can cost more than most families earn in years. 💸 RDF meets families right there, funding the treatment costs that matter most. 💉

Your donation is the reason a family stops fighting this alone. Give Hope for a Lifetime. 🩵 giving.sg/rare-disease-fund

This word shapes a life story from day one. ☝🏻 Most rare diseases aren't something patients caught or could've prevented...
05/08/2026

This word shapes a life story from day one. ☝🏻 Most rare diseases aren't something patients caught or could've prevented. They're written into who they are. 🧬 What can change is the support they receive. 🙏🏻

To donate, go to giving.sg/rare-disease-fund 💫

03/08/2026

For Christopher's family, one answer changed everything. Not the diagnosis. Not the years of appointments. The approval. ✅

That's the moment RDF exists for, not just to fund treatment, but to be the reason a parent doesn't have to carry it alone. 💫

Every donation is someone else's "we did not feel so alone.” Give Hope for a Lifetime: giving.sg/rare-disease-fund 🩵

01/08/2026

👩🏼‍⚕️ Nurses show up in the moments no one else sees: the 3am check-ins, the calm voice during a hard diagnosis, remembering a patient’s name after hundreds of others.
That doesn’t happen once a year. It happens every shift, for every patient, whether anyone’s watching or not. 🕣

Today, we just wanted to say it out loud. Thank you. 💙 Happy Nurses Day!

Disclaimer: This video contains dramatized scenes featuring actors. The individuals portrayed as patients and healthcare professionals do not represent real patients, actual medical cases, or specific healthcare providers. All scenarios and portrayals are for illustrative purposes only and do not constitute professional medical advice.

SGCares givingsg

Tiny, invisible, yet essential. When the body can’t produce enough, everyday functions can fail, but the right treatment...
29/07/2026

Tiny, invisible, yet essential. When the body can’t produce enough, everyday functions can fail, but the right treatment can change lives.

That’s what RDF makes possible. 🩵 Give Hope for a Lifetime: giving.sg/rare-disease-fund

3 more rare diseases. 3 more chances at treatment. 🩵🧬Since the start of 2026, RDF has expanded support to cover Plexifor...
27/07/2026

3 more rare diseases. 3 more chances at treatment. 🩵🧬

Since the start of 2026, RDF has expanded support to cover Plexiform Neurofibromas (NF1), Fabry Disease, and Long-Chain Fatty Acid Oxidation Disorders — meaning more families now have a path to the treatment they need. Swipe through to see what's new →

Every donation goes directly toward treatment costs for these conditions and more. Help us keep expanding what's possible.

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100 Bukit Timah Road
Singapore

Telephone

+6563942329

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