Help find answers and a treatment plan for a very rare and difficult diagnosis so my daughter can live.
Auckland
This is my last resort, I am a single mum of three, my name's Samantha,
Raven is 18 and loves art, tattoos and is an absolute animal lover.
Raven has a very rare condition (suspected SMA) superior mesenteric artery syndrome, 33% of people with this condition lose their battle. Ravens condition is creating constant pain nausea vomiting and weight loss (22 kg in 12 months) Due to The difficulty in finding a diagnosis in the public system (6yrs) I am desperately wanting them to be seen by a private gastroenterologist clinic in Auckland. In the meantime while there is no definite diagnosis my child continues to loose weight and is in more severe pain and nausea resulting in 2 hospital stays in 2 months this year.
With no treatment other than pain meds as all nausea medication appears ineffective. My fear is that unless I am able to access a private specialist my child’s condition may progress to where they’re not able to be helped. Last week, in 1 week even with great effort from Raven they lost 2kg, they’re 5.7 ft and 49 kg. I have found a private nutritionist and have started Raven on a high protein and whole foods diet in a hope to slow the weight loss while we wait. Any help at all from anyone would be more than appreciated, I see it as you saving my beautiful, strong and courageous child. They need all and any support you could give big or small ❤️God bless all
I am Very blessed to be Ravens mum ❤️
Funds will be spent on accessing a private gastro centre here in Auckland. Cover the cost of consultation, and tests. Nutrients and supplements.
Change of payee 28 April 2022
Funds will be paid to Samantha on behalf of Raven.
🙏💜thank you so much Alan, really appreciate it. Sorry for my late reply ✨
💖💜love you too 💕thanks Storm ✨
❤️💖Thanks so much Tiaan ✨
🙏💖thank you so much xx
❤️❤️❤️❤️thank you so much Mallory ✨🙏means so much to Raven and me
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