Thank You Everyone RE: Re: MRSA questions

July 18, 2003

Hello Kim!

a had clinic today, everything is find. I mentioned the

magnesium and tea tree oil to our doc, and the different things that

you have written. I was pleasently surprised when he said " I am not

against alternative medicine " . " Just use your judgement and make

sure you know the source " . I did not ordered the tree tea oil, I

ordered the lema oil, now I wished I had ordered the tree tea oil,

since I probably would have saved some money on the shipping, too

late. n posted some really good website links on sharktank,

very informative, worth saving, for future reference, about tree tea

oil.

I think I have told you this before but for a long time a was

asyntomatic and one thing that she did, was drink lots of milk and

get this, cranberry and grape juice!!! Any link to what you have

written below??

She got sick when she quit drinking milk and her juices, coincidence?

I only cook with olive oil and she only will eat butter, but on the

other hand she eats a lot of chocolate, she craves chocolate.

Sorry, this is so crazy the way I am writing but I am writing as I

remember what you wrote below and it makes so much sense, it is such

a paralel to a's life.

Well, thank you for sharing your knowledge, no matter how much I

read, there is no way, I could have come up with this information, in

plain english as you write it.

Growing up I used to get really bad bronchitis, my cf gene??, and my

mom would make me drink all this herbs stuff, and do garggle with all

this horrible leafs, and I used to cry but I wish I had pay attention

to what they were. I doubt I could find them here in the USA, our

flora is so different, but I least I would know.

Love to all of you,

mom of a 9 wcf, Venanzio 7 nocf, Pepe 3 nocf

> I'll be headed out to the mall today to find Manuka oil. In a few

> weeks we should know if it's working. I'll send a response to the

> group. Why do the CF foundations not know about tea tree and manuka

> oils? The news needs to get out to everyone in the CF community.

>

> Mindy

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