Monday, June 10, 2013
Worth Considering
No, I don't think everyone has Lyme disease now, not at all.
But some of you reading this may want to get tested for it!!
If I hadn't joined the support group on Facebook and seen the photos I'd be none the wiser.
Sharing information, which may be relevant to you or not, but if it helps just one person not suffer like we have then it's worth it.
If you have been diagnosed with CFS/ME, Fibromyalgia, Lupus and in some cases MS then you have nothing to lose.
Or you may not have been diagnosed with anything at all, but you have ongoing seemingly random health issues, and not just physical ones.
Do you live in any of these areas? Or have you ever?
From what I have read Geelong and Newcastle are 'hot spots' for diagnosis' of Lyme, along with some parts of WA
Our positive results for 'Rickettsia' or 'Scrub Typhus' can only have come from a paralysis tick.....
G
x♥x
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3 comments:
Really ?
Newcastle ?
Seeing the Doc this week, will bring it up with her- i have been diagnosed with CFS.
Interesting reading Gina x
FBC, UEC, LFT, G6PD, Rickettsia, Mycoplasma, Chlamydia Pneumonae (this is not the STD strain BTW), EBV, Parvovirus, HHV6.
Is what we were tested for.
I don't mind if you use us as an example Lisa.
Tell your Doc that Lichen Sclerosis is considered by some to actually be Bartonella infection and treatable with antibiotics xx
http://www.lymediseaseaction.org.uk/about-lyme/neurology-psychiatry/
This is quite a good article
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