To asisist with medical intervention overseas to aid in helping Tracey obtain remission for SLE and be well and healthy.
Whangaparaoa, Auckland
My name is Tracey Brown, and I live with Lupus (SLE). It’s an autoimmune disease where my own body attacks itself,
Lupus doesn’t follow a script. The exhaustion I feel isn't just being tired; it's a deep fatigue that sleep can't touch. Beyond the physical toll, there’s a heavy emotional weight. Lupus affects my body, my spirit, and my precious time with my husband and family.
Eight months ago, my battle escalated. Lupus began to attack my digestive system. Eating became a nightmare. The constant pain, nausea, and vomiting led to severe weight loss. My body couldn't absorb nutrients, causing it to starve. To try and fix these issues, I've had multiple surgeries to separate adhesions and even a resection of my intestine. Sadly I’m still not recovering.
My purpose is to serve others. I have a deep passion for supporting families in their time of grief and loss,as a funeral director at Hibiscus Funerals. While my body fights an invisible war, my heart and spirit are dedicated to helping others.
This journey is proof that even in the midst of immense personal struggle, we can still find a way to serve a greater purpose. I call this a “life glitch,” and I have not given up. I've learned that courage is not the absence of fear, but the ability to act in spite of it. I am not defined by my illness, but by my resilience and my unwavering belief that with help I to can achieve remission.
Thank you all so much for your love, kindness and support.
Forever grateful,
Tracey Brown
Funds received are to assist with the cost of seeking international medical treatment from specialists and surgeons, accomodation while away from home, medications required and hospital stays.
Sometimes you just give up. 17 December 2025
I wanted to update you all on our journey and how easy it is for us to give up and not know where to go or turn and we just kind of go… “ oh well” what can I do. The walls are up.
Since my return from the states NZ would not fill the script from my specialist. The cost to fight just made everything impossible. I gave up… I put my self back into the public system and spent the last two months being robbed of my quality of life again as they just passed me around and promised waiting lists of up to two years.
I am stuck ! So I decided to flip the mindset and decided I could keep going down hill or I could just get on with it.
The large stent has been removed two weeks ago and it has made some improvement but I was discharged and not given any further plans. Told if you still can’t eat come back to ED.
So for now…. My hands are behind my back, and I am helpless as where to from here.
In New Zealand it is really a case of who has the most money survives.
I thank you all from the bottom of my heart for getting me this far and making my life so much better then it was before and yes, I am feeling much better then before I embarked on the search and treatment for a quality of life. It has ment so so much to me.
Little steps encouraged and helped by so may of you has made the biggest difference and I would hate to think where I would be if I didn’t see Dr wallace. He is life changing.
I tired… this flight right now is to hard.
Thank you for just being with me. 🩷
Thank you for your kindness and support. So Greatly appreciated. X🩷🌷
Luv you to Cuz. Thank you for your love and support 🩷🙏
I am completely blown away by your generosity and kindness. THANK YOU so very much for your gift. 🙏🙏 this has allowed for more time spent with the specialist. The specialist costs $1000 US per appointment slot. THANK YOU
Thank you both so very much 🩷
Thank you so very much for your kindness and support on my medical journey. 🩷🙏
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