Re: Allergie-immune again

[Guest guest]

The more traumatized the brain the more hypersensitive to any changes in its environment: hence the allergies ramp up. Hyper everything happens. Hyperacusis to those who had damage prior to the Lyme from the additional stress, light sensitivity to those who had prior visual cortex issues, increased allergies for everyone, especially the parietal lobe damage.

Choline helps to ramp down the allergies. Acetyl choline is good. Plenty of it. Ramps down some of those allergies.

To: Lyme_and_Rife Sent: Thu, January 21, 2010 10:51:45 AMSubject: Re: Allergie-immune again

Hi Susie,

I've never been tested for allergies but know that I have some. My AI test showed that I'm allergic to soy, wheat, gluten, and corn. I had been wondering about the gluten thing for a while. I also showed molds and 4 metals.

I'm beginning to think that a lot of my problems now are metals and not lyme. I have a mouth full of amalgams. After AI I plan on getting them removed. It isn't recommended during treatment. Who knows, after treatment it may not be an issue but I think it will.

What I have noticed so far is that I'm sleeping better, no meds for the first time in 20 years. That is major for me. I really can't say anything else at this point. I do know my urine is very smelly (sorry guys) and Gigi wrote me and said that is a good sign. I believe she said it means you are moving toxins. Also, BM's are sinking and she said another good sign. So so sorry guys for the visual. LOL

I've had a headache for 4 days now and I think what has happened is that I've been using the sauna. I didn't know not to until we get out the heavy metals. It can move them to the brain. I'm almost sure that's what has happened. I'm going to miss my FIR sauna but will not use it till it's time.

I'm taking chorella but need to get some other binders. She recommemded charcoal and micro silica which I don't have.

About a month ago I ended up in the ER with stroke like sx plus I passed out. I was paralyzed for a few minutes and couldn't talk. Very scary. I have episodes of not being able to use one of legs from time to time and this happened but this other stuff was added this time. My family called an ambulance. I couldn't talk to tell them not to. LOL All my tests were fine.

Anyone here have anything like this happen? I'm trying to figure out the culprit. I don't know if it's lyme or a co or metals. I never considered it could be metals until recently. I had been using the sauna very often when this happened so I'm thinking it could be the metals. This disease is so crazy.

Sorry I got long winded here.

Susie, if you want to see my report from AI I can send it to you. I don't mind at all. Anyone else for that matter. I think they are hard to understand. I get the gist of it though.

I hope you feel better soon Susie. I know how frustrating it is.

Connie

On Thu, Jan 21, 2010 at 8:38 AM, S & D Darrah <darrahssover (DOT) net> wrote:

Connie, have you noticed anything at all? what were your test results like? do you have a lot of allergies? i don't, but i'm hoping that it will calm the hyperreaction my body has to the neurotoxins.

i've been blaming how i feel on doing coiling for just a few seconds, but i'm off of everything (except essential supps and thyroid and sleep meds) and feel just as crummy and reactive up and down all day as with the coil. grrr. friday is the end of my first two weeks, then i'll send in another saliva sample.

i had a phone consult with my old llmd dr h, and he wants me to give low-dose naltrexone a try. i've wanted to for awhle. not sure i should start it while doing the drops...

it is a really good sign that you have in the past been able to get some health back, and i'm sorry you are down again.

xo

susie

Thanks for the nice welcome Thane and Susie.

I'll let you know Susie. I'm really hoping the AI will help. Only time will tell I guess. It's all I can do to not do other treatment at the same time but I know it isn't recommended. I really want to add rife but will hold off.

I'm so sick of abx although I did really good on the bicillin shots. I was able to do things I hadn't done in years. I wanted to give my body an abx break though. How long have you been doing AI and how are you doing on it?

Is it appropriate to discuss AI here?

Connie

On Tue, Jan 19, 2010 at 8:00 AM, S & D Darrah <darrahssover (DOT) net> wrote:

hi connie,

i'm the one on a-i. welcome, i'm so glad you are here, another old-timer to lyme. let me know how you do wth it. i always read here even if i don't reply much..

xoxo

susie

"I've been thinking" it's time that I introduce myself and tell you what I think of your group. First of all, I love this group just like it is. It's very caring and close knit and I like that a lot. I've been reading here for a while but since I don't rife I didn't know if I belonged. I was looking into it and haven't given up the possibility at a later time.

Anyway, my name is Connie and I'm definitely not new to lyme. I've been sick since 1989 but was dx'd with CFS/FMS. In 2004 I finally found out about lyme and was tested and it was positive.

I've been in treatment since early 2005 with abx. I've been unable to work for the most part of the 20 years. I'm much better but still not able to work unfortunately. In Sept.09 I went off my bicillin shots that I had been on for over 2 years and did OK for a couple of months then BAM!

I don't want to make this too long so won't go into anything else other than the only thing I'm doing right now is AI. I think I read here where someone was doing it or it could have been another group. I just started it last week.

I hope you can tolerate my broken up paragraphs, I have lots of neuro problems and have trouble reading one big paragraph so I always write like this.

Thane, I have to commend you. You do a great job here with the group. You are a genuinely nice guy. I'm a very good judge of character. LOL

Connie

On Tue, Jan 19, 2010 at 6:46 AM, malindabross <malindabross@ gmail.com> wrote:

Thane you are too kind!I am sorry too, if I sounded as if I was scolding.... .definately not! God bless ~ Malinda> > >> > > I've been seeing how our group has been morphing lately from one that keeps> > personal chit chat to a minimum and focuses mostly on treating lyme to one that> > includes more personal off topic discussions and less about lyme. So I wanted> > to ask you all, What kind of group do you want? Because i'm not sure we can> > have both.> > >> > > In a group that is mostly lyme information focused there seems to be higher> > quality information shared and new members feel less intimidated to join into> > the discussion. And in a group where we act like old friends and feel free to> > talk about many things non lyme related we find more emotional support, which is> > just as important, but we can come across more cliche-ish, discouraging some

new> > members from joining the discussion and asking their questions. I guess I have> > always wanted our group to be a place where sick new members can find informed> > people willing to help and not have to sort through Off Topic posts that exhaust> > their precious little energy. I'm probably not the only one who has noticed> > that we get very few new members asking questions anymore. And that to me is a> > tragedy because there are so many wonderful people here who could offer helpful> > suggestions. And it seems its those new questions from members that spurs the> > very best lyme discussion.> > >> > > I want to reassure you that though I am the moderator of this group, it is> > YOUR group, and its you who choose what you want from it. I am fine with it> > staying the smaller closer nit group we have now that enjoys the

freedom of> > talking about a whole variety of issues if thats what you want, but just so> > people understand that its discouraging some new members from joining the> > discussion.> > >> > > I of course still boast we've got the best group on the net! > > >> > > Thane> > >> >> >> >> >> > Tue Jan 12, 2010 8:16 am> >> > Show Message Option> >> > "malindabross" <malindabross@ ...>> > malindabross > > Offline > > Send Email > >>------------ --------- --------- ------If your post is not about electronic devices used in the treatment of Lyme then please put an OT: in the subject line.------------ --------- ---------

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