The rare illness called Lyme disease needs to be made public and be treated as a big health issue we are having today!!! In many cases these days doctors/specialists will misdiagnose the disease and then realise the issue but it's all too late.
This tragedy has happened to a very good family friend of mine, and it just breaks my heart. Tracy Fitzgerald is one of the most positive, kind, caring, bubbly people I know. While going through all kinds of trouble trying to have children, she finally fell pregnant to a beautiful boy Zac who is now 11yrs old. While pregnant over in Malaysia she remembers getting bitten by a tick and going to the doctors about it. The doctors misdiagnosed the issue by telling her it could be just an ingrown hair.
Tracy's problems just got worse with not knowing what is wrong with her. She's been to many specialists in the past 5 years with each giving her different theories of what the problem is.
It's now too late for a simple antibiotics to heal her disease. Not only have they had to hear this reality. This disease may have been passed down to her son Zac who is showing early symptoms relating to the disease.
Her only option now is to either pay $30,000 in Queensland or $20,000 to go to Cyprus to get the professional help she needs to cure this ugly disease.
If we can please help this beautiful family ease their stress just a slight would be greatly appreciated. Your generous heart would be forever appreciated.
Please your donation or you sharing this to your network of friends could cure someone from this disease.
- Lisa Wakeham
- Hart family
- Vana Lads
- Josh Simpson
- sam pultar
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