posted
Hi, i copy paste my message in this section, i send it in general support first, i think here you will maby more answer me...
I started my medication tree days ago, and id like to have your opinion of my treatment.
Im french so hope youll understand what medocs it is...
Meprone: Monday,wednesday, friday= half of a tea spoon twice these day for a week after one tea spoon twice a day for these days =tells it kills babesia
Rifampin=for bartellonna(i saw for some it doenst work... ) Tuesday, thursday and saturday, twice a day
Zitromax= once a day all the week
Apo-Fluconazole=every days
I also have a lot of supplements like magnesium, Vit C, Chelators, zinc,that i already took for my mercury...
What do u think of these combo of medication for my little ennemis??
Im totally affected by bartellona too...Paniqued and suicidal...don't want to see anyone....
this is all new for me, and i don't even realize all this...Im alone, nobody understand how it is suffering...At least now i know im not crazy...
These ****ing emergency doctors who told me that my tachicardia and my panic, my twitching, my breathing problems, my horrible pain everywhere, even in my ears and ribs was fibromyalgia!!!!!Even my loss of hair!!! I m so frustrated.
And all my blood test clearly indicated bacteria in my blood.by the neutrophyls and lymphocites ..That my doctor saw at the first look(environnemental doctor, wonderful!)
They don't even test for lyme in my province...And a lot of fibromyalgic people have lyme without even knowing the existence of lyme disease!
And the labo here, if a doctor thinks of lyme, is ELISA< proved to be bad...and don't test for co infections...
I tested for lyme at Igenex, and co infections at Fry Lab. very good pace, they even send pictures of your little friends...I will see them on monday...
I feel like in a nighmare, a horror movie everyday, since months...I have no minute of rest, im tired and have pain everywhere but i can't stay calm, im paniqued..
And so frustrated...I saw the letter to oprah, hope something will arrive for us...for the believe of the chronic lyme,
how can it be rejected, parasites can't take 30 days to leave, how can they think that???
Im with everyone of u, pray for u and think of u, we must help and support each others if we want to survive....Hope my english is not so bad...
Hope youll tell me your opinions of my treatment that my doc started for now...I think she planned to repeat all this 6 times,to begin... As u see, she seems to treat all the infections at the same time..she went study lyme disease in usa.
She was hopping to put me on an iv because she says im very affected,and she was hopping to find an open mind doctor in Quebec, but knows it will not be the case, she knows she won't find one...And it will be like this until one doctor have his child affected by lyme disease...
Thank u...
a heart broken... Fannie
-------------------- Lyme-co infections Posts: 27 | From Canada | Registered: May 2008
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