MNDa Singapore

MNDa Singapore Our vision is for every MND Patient and Caregiver to live their Lives with Dignity, Care and Hope.

Established on 27 April 2021, we are a group of Warriors with Motor Neurone Disease (MND), Caregivers and family members, Volunteers and Healthcare Professionals πŸ€—

Join Us, Donate or Volunteer: linktr.ee/mndasg

On 12 July 2026, our MNDaSG family came gathered at SAFRA Toa Payoh for a fun-filled afternoon of football, food and com...
30/07/2026

On 12 July 2026, our MNDaSG family came gathered at SAFRA Toa Payoh for a fun-filled afternoon of football, food and community spirit!

After the final whistle, we headed over to Syed Cafe Exclusive for a well-deserved Post-Screening Lunch, tucking into Thai Mee Goreng, Nasi Goreng and Aglio Olio Dory.

We also had a little pre-game fun: members placed their names into the container of the team they were rooting for. Names drawn from the winning team's container walked away with small prizes β€” and true to our community spirit, we made sure the other side went home with a little something too! 🎁

A huge thank you to our two amazing supporters who made this outing possible:
🌟 SAFRA Toa Payoh for the venue and screening experience
🌟 Syed Cafe Exclusive for the delicious spread that fueled our afternoon

Thank you for being part of these special moments with us! πŸ’«

πŸ“± Find out more: linktr.ee/mndasg
πŸ’™ Support our cause: giving.sg/donate/campaign/mndasg-waves-of-hope

5 more days to the end of our campaign! Help us reach our fundraising target πŸ’™
25/06/2026

5 more days to the end of our campaign! Help us reach our fundraising target πŸ’™

Meet Kok Peng and Wanqi, our last feature in this run of . πŸ’™Kok Peng is one of our co-founders, diagnosed with ALS, and...
25/06/2026

Meet Kok Peng and Wanqi, our last feature in this run of . πŸ’™

Kok Peng is one of our co-founders, diagnosed with ALS, and a passionate advocate for assistive technology for MND patients. Despite losing voluntary control of his muscles, he continues to live with purpose β€” using eye-tracking technology to communicate, write, and stay connected with the world.

Wanqi, his wife, has been by his side through it all ❀️ Together, they show us what love and resilience looks like when life doesn't go as planned.

Kok Peng's story has been featured across multiple platforms, from CNA to Our Grandfather Story, and he was also recognised with the 2024 Goh Chok Tong Enable Award (Promise).

πŸ”— Learn more or support our community at linktr.ee/mndasg
πŸ‘‰πŸΌ Visit our fundraising campaign to make a difference: giving.sg/donate/campaign/navigating-the-mnd-odyssey

Global MND Awareness Day may be over, but the stories don't stop here πŸ’™Meet Whee Jim and Elizabeth, our latest feature i...
23/06/2026

Global MND Awareness Day may be over, but the stories don't stop here πŸ’™

Meet Whee Jim and Elizabeth, our latest feature in .

Whee Jim was diagnosed with ALS in 2023, and his story has been captured beautifully by two incredible features. "Living With A Fatal Disease As An ALS Patient" by Our Grandfather Story, and "A Life Measured in Meaning" by the Community Foundation of Singapore. They both paint a picture of a man who has chosen to live with purpose, generosity, and grace.

Elizabeth is his caregiver today, and together they show us what dignity in care really looks like.

Whee Jim also established the Lok Yan and Whee Jim Fund in memory of his late wife, supporting disadvantaged children and young caregivers balancing school with caregiving responsibilities.

🀍 Learn more about the Lok Yan and Whee Jim Fund: bit.ly/ly-and-wj-fund

πŸ”— Learn more or support our community at linktr.ee/mndasg
πŸ‘‰πŸΌ Visit our fundraising campaign to make a difference: giving.sg/donate/campaign/navigating-the-mnd-odyssey

Today is also...✨Global MND Awareness Day ✨1 in 300 people will develop MND in their lifetime and there is still no cure...
21/06/2026

Today is also...
✨Global MND Awareness Day ✨

1 in 300 people will develop MND in their lifetime and there is still no cure.

Today, MND associations around the world come together in solidarity with everyone living with Motor Neurone Disease, their families, and caregivers. United for hope, strength, and global solidarity. πŸ’™

Here's how you can show up today:οΏ½πŸ’™ Hear our voicesοΏ½πŸ“’ Share this post and raise awareness�🀝 Volunteer, donate, or simply check in on someone you know with MND

Every action counts!

🌟 Donate to MNDaSG: bit.ly/mndasg-ntmndo
πŸ”— Get involved: linktr.ee/mndasg

Happy Father's Day to all the wonderful fathers and father-figures, both in the MND community and beyond. You show up wi...
21/06/2026

Happy Father's Day to all the wonderful fathers and father-figures, both in the MND community and beyond. You show up with strength, love, and wisdom every single day. Today, we celebrate you. πŸ’™

‼️ 16 days left for our donation campaign: "Navigating the Motor Neurone Disease Odyssey" ‼️The clock is ticking and eve...
14/06/2026

‼️ 16 days left for our donation campaign: "Navigating the Motor Neurone Disease Odyssey" ‼️

The clock is ticking and every bit of support counts now more than ever. From monthly outings and caregiver respite to AAC programmes and home visits, your donation keeps these services running for MND patients and their families.

✨ Every dollar goes further: all donations are matched 1-for-1 under the Enhanced Fund-Raising Programme (your $1 becomes $2 through Tote Board).

πŸ”— Learn more: https://www.toteboard.gov.sg/grants/enhanced-fundraising/
πŸ’™ Donate here: bit.ly/mndasg-ntmndo

16 days. Let's finish strong! Spread the word and share this with someone who cares. 🌟

Today's features Philip Yap (46, pALS) and Mavis, his wife and caregiver! The joy in this photo says everything about ...
10/06/2026

Today's features Philip Yap (46, pALS) and Mavis, his wife and caregiver! The joy in this photo says everything about who they are as a couple and as a family. πŸ’™

Philip was diagnosed with ALS in 2015, and his story has since touched many. An engineer by trade, he first noticed something was wrong when his fingers began fumbling with the tools of his everyday job. What followed was a diagnosis that would change everything - and yet, Philip and Mavis have faced it all with extraordinary resilience and an unshakeable spirit.

They have shared their journey widely and generously: through a SingHealth article, and alongside Mdm Teo and Mr Ng in the deeply moving Channel 8 documentary, "Tuesday Feature | By Your Side: When Life Begins to Count Down".

And if that joyful, festive photo is anything to go by, they face each day with a whole lot of love and laughter too. πŸŽ„

πŸ”— Learn more or support our community at linktr.ee/mndasg
πŸ‘‰πŸΌ Visit our fundraising campaign to make a difference: giving.sg/donate/campaign/navigating-the-mnd-odyssey

Today's reminds us that love isn't just a feeling. It's a choice made every single morning. πŸ’™Meet Mdm Teo (ALS warrior...
08/06/2026

Today's reminds us that love isn't just a feeling. It's a choice made every single morning. πŸ’™

Meet Mdm Teo (ALS warrior) and Mr Ng (caregiver), a couple in their 70s who have been navigating life with ALS since Mdm Teo's diagnosis in 2017.

Their story was beautifully captured in a Channel 8's "Tuesday Feature | By Your Side: When Life Begins to Count Down". When life feels precious and time feels tender, Mr Ng has chosen to show up for his wife with unwavering love and quiet strength. It is a love that has weathered years, and continues to show up even in the hardest seasons of life, quietly and faithfully, every day. πŸ’™

We are deeply honoured to feature Mdm Teo and Mr Ng, and grateful to Channel 8 for telling their story. πŸ™πŸΌ

πŸ”— Learn more or support our community at linktr.ee/mndasg
πŸ‘‰πŸΌ Visit our fundraising campaign to make a difference: giving.sg/donate/campaign/navigating-the-mnd-odyssey

ALS Awareness Month may be over, but the fight against ALS continues. From here on, will be a little different. Becaus...
05/06/2026

ALS Awareness Month may be over, but the fight against ALS continues. From here on, will be a little different. Because behind every pALS is someone walking the journey right alongside them. πŸ’™

Meet Mark (44 years old, ALS Warrior) and Aisyah (36 years old, ALS Caregiver) - husband and wife, and two of the most inspiring advocates we know.

From a feature in Berita Harian, to a radio recording on CNA 938, to sharing their story openly on Instagram, they have made it their mission to pull ALS out of the shadows and into the conversation. Even their children walk this path alongside them. A reminder that when a family faces something this big, they face it together.

Their courage in sharing their story is helping others feel less alone and we are so grateful for everything they do for this community. πŸ™πŸΌ

Head to their Instagram accounts ( and ) to follow their journey, and check out their Berita Harian article, CNA 938 recording, and caregiver video ().

πŸ”— Learn more or support our community at linktr.ee/mndasg
πŸ‘‰πŸΌ Visit our fundraising campaign to make a difference: giving.sg/donate/campaign/navigating-the-mnd-odyssey

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