Bare inquiry link (Sally)

[Guest guest]

Hi Sally,

I found a link for inquiries about the Bare machine (updated Dec.'09) on this webpage:

http://www.rifetechnologies.com/

Scroll down until you see the inquiry link - just click on the name, " Bare", and it will connect you to his email. I think that's the only way to get more info on the Plasma Two machine. The other available items are listed on the Plasma Sonics website, with prices, http://www.plasmasonics.com/Product.html

I also found some older online audio interviews with Bare. In order to get the stream, "right-click" on the "listen" button, then "save target" to your desktop. I was able to listen to the interviews in winamp, but they are for streaming only (I could not save the interview itself).

I also could not stream them directly by clicking "listen" button. I could listen to them only after saving the links to my desktop. It could have something to do with the fact that they are not current.

summary (non-audio):

http://www.lauralee.com/bare.htm

audio from 2003:

http://www.lauralee.com/index.cgi?pid=3029

audio from 2000:

http://www.lauralee.com/index.cgi?pid=3229

- Jane

From: Darlington <richardd9229@ yahoo.com> Subject: Re: Re: MMS for EBV? (was) salt/C for EBV? To: Lyme_and_Rife@ yahoogroups. com Date: Friday, July 2, 2010, 3:29 PM I've been using the MMS#2 every 2 hours for a week now and the taste is almost

non-existant and it doesn't bother my stomach a bit like the MMS #1 does. I also notice a nice improvement in my health. MMS#1 cannot be taken with so many things for 3 hours on either side of it that I'm not sure how anyone takes it except for first thing in the morning and last thing at night. At first it was only Vit C you couldn't take within a few hours of it but now it's protein and fruit and a whole list of anti oxidants. I don't know if the MMS #2 has the same restrictions but it's MUCH easier to take and my stomach is fine as long as I drink a glass of water with each pill. ________________________________ From: Clemens <denise_clemens@ yahoo.com> To: Lyme_and_Rife@ yahoogroups. com Sent: Fri,

July 2, 2010 8:56:57 AM Subject: Re: Re: MMS for EBV? (was) salt/C for EBV? Ann, I've never taken the capsules but some people have shared that they are worse on the stomach. As for taking the MMS and getting heartburn, I had this problem too. I take it about 45 minutes after I've eaten a solid meal. I swallow a couple of spoons of yogurt, take the MMS, and follow with a few more spoons of yogurt. This works well for me - no heartburn, stomach upset, cramps, or diarrhea - all problems I've suffered taking MMS orally any othe way. I get a little tired of having to eat so much in order to take it and I only take it twice per day at most, after breakfast and after supper. ________________________________ From: Ann <anncooper10@

yahoo.com <http://yahoo.com/> > To: Lyme_and_Rife@ yahoogroups. com Sent: Thu, July 1, 2010 12:26:20 PM Subject: Re: MMS for EBV? (was) salt/C for EBV? Has anyone tried MMS 2 which you can put in capsules. I was thinking of trying it but wanted to get some input from others first. I found that MMS 1 was quite terrible tasting and gave me heartburn. I got up to 7 drops and had to stop. I'm wondering if the mms 2 would be easier on the system. I think you can order bottles aready in capsules. Yours, Ann > > Hi , > > Thanks for the MMS endorsement. You say you felt better from the very first time taking it, and that you'd never ever give it up. Can you tell me what you're taking it for, and what it's done to help? And also when you say you're sensitive to it and can't take more than 6 drops once or twice a day, what happens if you dose higher than that? Or more precisely maybe I should say what do you notice if you try to go above your usual dose? > > I'm very interested in this because I'm beginning to realize that so many people here really like it (well, not exactly "like" it, but recommend it) and feel it's been very beneficial. But I've taken so many

things that were supposed to help and didn't, that I now really like to hear from people who have actually felt the benefit, as opposed to the hype on websites selling whatever the product happens to be. > > Are you coiling in conjunction with MMS? Thanks so much for your input. > > Peggy > > Re: MMS for EBV? (was) salt/C for EBV?

> > Peggy, > > I am one of the culprits complaining and whining about the taste of MMS. Plus, I drank one shot of it down straight and nearly scalded my esophagus. However, I will never give up taking MMS, never. From the very first time taking it, I felt better. > > I am very sensitive to it and have never been able to take over 6 drops, 1 or 2x per day, and that's what I still take. Six drops was considered the maintenance dosage before the protocol was revised to less drops at a time, multiple times a day if needed. I work so I still stick with the 2x per day, and since I can manage 6 drops, that's what I do. > > Do not let the horror tales and complaints stop you. You can mask the taste in prune juice. In fact, I mix mine in a shot glass and knock

it down like it's whiskey. :-) I've got the shot glass in one hand and a chaser of cold water in the other and I slug down the MMS/prune juice and immediately slug down water next. I do this trying not to breathe through my nose so I don't get the bleach taste. > > Do not do MMS on an empty stomach, but not on a full one either. 45 min to an hour after a meal with no Vit C is fine. > > > ------------------------------------If your post is not about electronic devices used in the treatment of Lyme then please put an OT: in the subject line. -------------------------------