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Re: Re: Update and Qs about supplements/Vitamin C)

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Hi I am interested in the photo genie and clicked on the web line provided

by you, but then got a message to say that there is no such group. Is the

address exactly right? thanks Val Kavanagh

[ ] Re: Update and Qs about supplements/Vitamin C)

******Alice, this appears to be a great protocol.....how often do

you change

> things around? My protocol changes every 4 to 6 weeks,

depending on my blood

> reading. How much Samento (cat's claw) are you taking? I'm

back up to 27

> drops, 3 x's a day again. The time I was off it, I could feel the

difference.

> My doc took me off it after 8 months for I think it was 4 weeks,

then put me

> back on it. I also use the PhotonGenie daily and I am now

sleeping in the older

> model (pads only) at night, 7 days a week. The older model

" only " kills it,

> where as the newer Genie regenerates the sick/injured cells.

>

> Angel Huggzz

> or Angel

>

> SUBSCRIBE TO: PhotonGenieElectromedicine (email group)

>

PhotonGenieElectromedici

ne/

>

> LYME Disease MESSAGE BOARD

> http://www.activeboard.com/forum.spark?forumID=31898 &

ÿ sparkKey=5deb6043cb822f894a67a93a42ebc294b0

,

I don't see the doctor again until March, so my dosage will be the

same until then. I'm taking two capsules of TOA cats claw. My

doctor said I could take that or 5 drops. Quite frankly, I am

confused about a lot of things that I have heard from this group.

So many seem so much sicker than I am, but I've had it for so

long. Other are on such high doses of antibiotics and Cat's

Claw.how can what I'm taking be working so well?

I was mainly in a depression when I went to see my doctor. A

friend told me about her and went with me for the first visit. She

is a GYN/Wellness MD. I just wanted to see if there were some

vitamins or minerals that I might be missing. I was having color

loss in my left eye and tingling again in my legs, but didn't even

mention these to her because I've had things like that for 30-40

years and no one ever could tell me what was wrong even after

MRI's, blood tests xrays, etc. etc. I had quit going to the doctor

about most anything as things usually got better after several

months. But then it was always replaced by something else. I

didn't trust doctors and only went to this one because my friend

said that she really looked at you and did tests and asked

questions to find out about you as an individual and never just

tossed pills at you.

She is 2 hours away from me. She picked up on the Lyme

symptoms right away, asked lots of questions, and said I should

be tested, I was shocked.

Anyway, sorry to get OT..I only take antibiotics one day a week

and only one dose of two different antibiotics. I am very tired and

have to rest for two to three days. The rest of the time I am

starting to feel pretty good. I am getting my enthusiasm for life

back and sleeping less and less.

My eye is the most dramatic change. I went blind in my left eye

about 15 years ago. My site came back in about 6-8months. But

lately I had noticed that color was going in the left eye. (I had

been under a great deal of stress in my job and finally quit

because I just couldn't mentally or physically handle it anymore. )

I believe I wore myself out and allowed the lyme to take over

once again.

Anyway, after about three weeks on the meds, things started

coming out of my face and my eye cleared up. I still feel some

crawling on my cheek, but it is less every day. Bright light don't

bother me anymore and I can drive at night....

I think what I have in my face is Morgellions. Lucher from

this list, asked me if I had heard about Morgellons and I went to

the website and wrote her back that I didn't think I had them. But

since then, I have paid close attention to my face and have seen

the " threads coming out of my face. " I'm not crazy, I promise, they

are there and only on the left side were I feel the crawling. As

more and more leave, the crawling has gotten less and less. So

I think I do have Morgelions, just not as large as the photos on

the website.

www.morgellons.com

Once, 6 or 7 years ago, my face was ticking so bad it was drawn

up on my left side. It didn't go away but would come back from

time to time if I was stressed.

Anyway, I am thrilled to be on the way to getting rid of all of

this..and so glad to have something to fight against.

Sorry this was so long, it is very hard to talk to friends about this.

How do you tell someone you have worms coming out of your

face without them thinking you've truly lost your mind?

I'm going right now to find out about PhotonGenie? I am so new

to all this, but want to know everything I can to make myself well.

Thanks,

Alice

>

>

> > Dear

> > I'm on 10,000 units of vitamin C, cat's claw, and pulsing

> > antibiotics, vitamin e and several other natural things. The

Lyme

> > is leaving my head and face more everyday. My eye site has

> > returned along with the color that I was losing again. I think it

is

> > saving me after more than 35 years of lyme without knowing

> > what I had.

> >

> > I've added Salt in the last two weeks after asking my doctor

about

> > it. She said it couldn't hurt.

> >

>

> ******Alice, this appears to be a great protocol.....how often do

you change

> things around? My protocol changes every 4 to 6 weeks,

depending on my blood

> reading. How much Samento (cat's claw) are you taking? I'm

back up to 27

> drops, 3 x's a day again. The time I was off it, I could feel the

difference.

> My doc took me off it after 8 months for I think it was 4 weeks,

then put me

> back on it. I also use the PhotonGenie daily and I am now

sleeping in the older

> model (pads only) at night, 7 days a week. The older model

" only " kills it,

> where as the newer Genie regenerates the sick/injured cells.

>

> Angel Huggzz

> or Angel

Questions and/or comments can be directed to the list owner at

-Owner

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