The Sweet Heist

24/07/2026

Good Day All

Please note we will be unavailable until further notice due to a family emergency.

12/04/2026

The Team at Sales Heist would like to say a huge congratulations to Kelly Du Plessis, Founder of Rare Diseases South Africa NPO 120-991 on being chosen for a Health Department advisory board.
This is so well deserved, thank you for everything you and your team do Kelly!

03/04/2026

The Sales Heist Team would like to wish our Jewish and Christian supporters Chag Pesach Sameach and a Blessed Good Friday and Easter Weekend!

21/03/2026

To all our supporters who celebrate,

Eid Mubarak!

May your life always be filled with peace, happiness, and success and your heart always remain filled with faith, kindness, and hope.

04/02/2026

04/02/2026

Day 4 of Rare Disease Month 💙

Today we share the powerful journey of Vimla , whose life changed completely after the sudden onset of severe autoimmune illness.
Her journey includes intense treatments, loss of mobility, repeated hospitalisations, vision complications, and even a near‑fatal cardiac event during chemotherapy. Despite these unimaginable challenges, Vimla continues to fight for proper care, stability, and recognition of her condition.
Her strength reminds us that chronic illness is not just a medical battle, it’s an emotional, physical, and financial one too.

Read her full journey on our blog:
https://www.rarediseases.co.za/post/vimla-redddy-medical-personal-statement

04/02/2026

Day 3 of Rare Disease Month 💙

Today, we share the inspiring story of Narishka Fourie, whose life changed at just ten years old when a day at the movies became the beginning of her rare disease journey. Now 18, she lives with Marfan syndrome, Chiari malformation, and scoliosis, three rare conditions that have shaped her path but have never dimmed her strength, talent, or voice.

Her story is one of courage, self-discovery, and rising above the limitations placed on her from a young age. From hospital rooms and countless medical tests to navigating school with misunderstood conditions, Narishka found resilience she never knew she had. Today, she is a musician, writer, model, and patient voice ambassador, using her platform to advocate for understanding, awareness, and empathy for those living with rare diseases.

Narishka reminds us that:
“Your story matters,and it might be exactly what someone else needs to hear.”

Read her full journey on our blog:
https://www.rarediseases.co.za/post/from-popcorn-lines-to-hospital-rooms-my-life-changing-rare-disease-journey

04/02/2026

Day 2 of Rare Disease Month😃

Today we highlight Ramohlale Mmaphuti, who has been living with Trigeminal Neuralgia for 10 years, a rare condition often described as sudden, electric shock–like facial pain. Though invisible to many, her journey reflects strength, resilience, and the reality of living with a rare disease.
As Trigeminal Neuralgia warrior Ramohlale Mmaphuti reminds us: “It is rare, but it is real.” 🩵
Read her story on our website blog: https://www.rarediseases.co.za/post/living-with-trigeminal-neuralgia-my-10-year-journey