Fight for Zach

Fight for Zach A page about a boy with MPS2, living his best life

14/03/2026

South Africa's leading online store. Fast, reliable delivery to your door. Many ways to pay. Shop anything you can imagine: TVs, laptops, cellphones, kitchen appliances, toys, books, beauty & more. Shop the mobile app anytime, anywhere.

14/03/2026

Zach needs your help ๐Ÿฆ–

He is due to have the 2nd of 2 very important surgeries on his hands to make is life easier and help with his hand mobility and function and relieve the discomfort and pain he has.
However there are costs not covered by the medical aid even though it is directly linked to his disease which is a PMB.
We need help raising the funds for the upcoming surgery and day to day expenses for Zach,

Please share and donate if you can ๐Ÿ™

The 1st surgery last October made a huge difference for him, so the 2nd surgery is really important for him.

Thank you ๐Ÿฉต

08/03/2026

Looking for a way to help?

Check out Zach's wishlist

Deliveries can be made to:
JHouse
Bowden Business Park, 12 Langkloof St, Alrode South, Alberton, 1451
Weekdays 8am to 4pm

South Africa's leading online store. Fast, reliable delivery to your door. Many ways to pay. Shop anything you can imagine: TVs, laptops, cellphones, kitchen appliances, toys, books, beauty & more. Shop the mobile app anytime, anywhere.

28/02/2026

๐ŸŒ๐Ÿ’œ Today we stand with the 300 million people living with a rare disease. We are united with their families, friends, caregivers, advocates, and the medical professionals, researchers and organisations that working tirelessly to build a more equitable future for our community.

Together, weโ€™re showing our colours, raising awareness, and inspiring change by talking about what equity means to us.

Thank you to everyone whoโ€™s taken part, whether youโ€™ve lit up your home, shared your story, joined an event, or supported someone you love. By standing together weโ€™re proving that our community is strong, united, and truly more than anyone can imagine. โœจ

๐Ÿ‘‰ Learn more and discover ways you can still get involved: https://go.rarediseaseday.org/NEWS

28/02/2026

Today (28 February) is ๐‘๐š๐ซ๐ž ๐ƒ๐ข๐ฌ๐ž๐š๐ฌ๐ž ๐ƒ๐š๐ฒ! ๐ŸŒŸ

Rare Disease Day is the globally coordinated movement for rare diseases, to raise awareness and generate change for the 300 million people worldwide living with a rare disease, their families and carers.

You can show your support of people living with a rare disease by sharing the '๐ˆ ๐’๐ฎ๐ฉ๐ฉ๐จ๐ซ๐ญ ๐‘๐š๐ซ๐ž ๐ƒ๐ข๐ฌ๐ž๐š๐ฌ๐ž ๐ƒ๐š๐ฒโค๏ธ' pledge. This graphic is available to download in different languages via the official Rare Disease Day website: https://www.rarediseaseday.org/

28/02/2026

Today we recognise Rare Disease Day, a movement raising awareness for the millions of people worldwide living with rare diseases.

While each condition may be uncommon, the challenges faced by patients and their families are shared: delayed diagnoses, limited treatment options, and barriers to care. Rare diseases is a cause close to our hearts, and we remain committed to advocacy, awareness, and meaningful support.

Because rare is many, and every voice matters

Nothing like a video call with sissy to put a smile on his face โค๏ธโ€๐Ÿฉน
22/01/2026

Nothing like a video call with sissy to put a smile on his face โค๏ธโ€๐Ÿฉน

A very hangry little dinosaur waiting his turn... ๐Ÿฆ–
21/01/2026

A very hangry little dinosaur waiting his turn... ๐Ÿฆ–

Settling in for a long day ๐Ÿ™ˆKitted out ๐Ÿฆ–๐Ÿ๐ŸŽง
21/01/2026

Settling in for a long day ๐Ÿ™ˆ
Kitted out ๐Ÿฆ–๐Ÿ๐ŸŽง

Address

Alberton

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