Laura Bruno's Blog : I found this thought provoking article and want to share it.
(Click title for full article)
"I will share some of those things in this article. As I explain in the book and in other articles, Lyme Disease tends to affect people who have big things to offer the world."
"Lyme seems to show up like a roto-rooter, forcing people to dig deep and remove ALL blocks to creativity and healing."
Thursday, 30 June 2011
Saturday, 18 June 2011
Why is Borrelia so hard to kill ?
This is a very informative video put together by Connie Strasheim. I finally understand what Biofilms are now. :-)
Friday, 3 June 2011
1989 : Lyme Disease - a new disease in southern Africa...
This article was written in 1989... ! (click link)
I want to know why when in 1996, seven years after this article was written, when I told my GP that I was 100% sure I had Lyme disease, he told me "impossible - you can only get that in the USA." Urgh... !!
I could have received treatment way back in 1996 and not be bounced from specialist to specialist with no outcome for another 15 years... In 2000 I was told I proabaly had the early stages of MS, then in 2005 after another MRI of the brain I was told, Not MS, could be Lupus, could Sjogren's disease, could be Lou Gerhig disease, could be Epstein Bar.... etc., etc. I was put on Lamictin for epilepsy... for several years, then when my liver started to play up I was put on Neurontin because it 'may have been' the Lamictan causing terrible enzyme levels.
It is really NOT fair!! and I am not the only one in this boat in South Africa. In December 2010, the Department of Health in South Africa told me it was impossible for me to have got Lyme disease in South Africa...
"The status of Lyme disease in southern Africa is presently unknown but preliminary evidence indicates that the disease may occur in humans in the Republic of South Africa. The abundance of hosts and tick vectors would favour the establishment of the infection in Africa"
I want to know why when in 1996, seven years after this article was written, when I told my GP that I was 100% sure I had Lyme disease, he told me "impossible - you can only get that in the USA." Urgh... !!
I could have received treatment way back in 1996 and not be bounced from specialist to specialist with no outcome for another 15 years... In 2000 I was told I proabaly had the early stages of MS, then in 2005 after another MRI of the brain I was told, Not MS, could be Lupus, could Sjogren's disease, could be Lou Gerhig disease, could be Epstein Bar.... etc., etc. I was put on Lamictin for epilepsy... for several years, then when my liver started to play up I was put on Neurontin because it 'may have been' the Lamictan causing terrible enzyme levels.
It is really NOT fair!! and I am not the only one in this boat in South Africa. In December 2010, the Department of Health in South Africa told me it was impossible for me to have got Lyme disease in South Africa...
"The status of Lyme disease in southern Africa is presently unknown but preliminary evidence indicates that the disease may occur in humans in the Republic of South Africa. The abundance of hosts and tick vectors would favour the establishment of the infection in Africa"
- PMID:2699499 [PubMed - indexed for MEDLINE]
Wednesday, 1 June 2011
Lyme disease and an overload of bacteria and goggas in your body !!
This article is written by a fellow Lyme patient and I believe it has a lot of very good personal information in it.
People often wonder why they don't get 'better' after a short dose of antibiotics... The reason being... the bugs (parasites and bacteria) are not getting killed adequately!!
People often wonder why they don't get 'better' after a short dose of antibiotics... The reason being... the bugs (parasites and bacteria) are not getting killed adequately!!
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