Hello all, I live in Australia and our health authorities do not beleive Lyme disease is in the country..
It took me 15 months for a diagnosis as (1)only (1) doctor here in Perth beleives the disease is in Australia. I went to multiple doctors before hand and diagnosed with CFS etc etc... pretty much the same story as everyone else I would assume. It really is frustrating that Lyme disease is not recognised in Australia as I had to send my blood to the States (at a huge cost) for proper testing, finally with a result of Lyme, Babesia and Bartonella. Im currently taking oral antibiotics (Trimethoprim 300mg 2/day & Azithromycin 500mg 1/day) and then taking Tinidazole 500mg 4 in 1 day at the end of each month. I started the antibiotic treatment in June with not much herx, but how the ###### can I tell what is a herx reaction when I feel like crap most days. Anyway, I have ordered the cowden support program (1st month) a few weeks ago so fingers crossed it should be here within this week. I will keep you posted when I start the additional cowden protocol and I'll report how it goes.
F@#K Lyme......