Dear Lisa,
So good to see you here. I also had Lyme for 20 years and started out
really hard with IRT-- not in exactly the same way as you have, but it
was very, very difficult and I can relate.
Thankfully, IRT herxing will get you somewhere in all this, though, it
really will.
Are you Rifing and taking MMS alongside IRT right now? I'm thinking
that if you are, you should maybe take a break from them and just
concentrate on codes and rest for a good while. The body can only
handle so much, and those codes really give the body a lot of
information to utilize. You can always pick the Rifing and MMS up
again later down the road when you're stronger and have less herxing
with IRT.
You're so right when you say it is all about treating the whole
person, so right. The more I learn about that myself, the more
clearly and beautifully I see it. Just this morning I was reading
about a doctor who came up with physical proof of how chemicals
released by our emotional issues/belief system effects our cell
function. I'm so thankful to be using a method that addresses this as
well. True, full healing for many chronic disease sufferers cannot
occur without it.
Hang in there and keep up hope even though it might seem silly and
strained to do so at this point. Your beauty days aren't over! Some
of the best of them are just beginning...
Becky
--- In LymefreeIRT@yahoogroups.com, "west612908" <LisaMarie22@...> wrote:
>
> Hi everyone, I realize that some of you may know me from other groups
> but the questions that I have are specifically about IRT and any
> reactions that you all may have had that has possibly been like mine
> and how your out come has been if you have indeed been doing IRT for
> long enough.
>
> I just began class 17 and we have done 2 sessions so far. I have had
> lyme for 20 years or longer so I fully realize this is going to take
> some time to see large improvement. I also believe that with lyme, it
> is so insidious; that I am going to aim the full arsenal at it at all
> times and IRT is another big gun.
>
> I am home bound but I can do minimal house work and bathe, however the
> beauty days are over for me because there is no energy left to do any
> of that. I use my energies to stay alive. Although I have been Rifing
> for seven months and using MMS for 3 months I feel those thing (as good
> as they are) are just keeping me alive.
>
> To tell you the truth I don't want to do any of this stuff including
> IRT because I am tired of how sick it all makes me feel (HERXING) but
> on the other hand I am very great full they are out there because the
> alternative is a dirt nap.
>
> The first treatment put me on the couch for Wednesday and Thursday but
> really I thought to myself well this is not going to be unbearable, I
> can manage. That is until Thursday afternoon; my sister called me and
> told me that her son has cancer. As I was crying over that I got the
> most intense headache I have literally ever had in my life. I could
> feel the vessels in the back of my head shooting pain through there
> branches up through the top of my head.
>
> I went and got an ice pack and wrapped it around my head and felt
> crummy for the rest of the day. The next morning I got up and literally
> had to shuffle around, my legs were so heavy it felt like I had rocks
> in my pant legs. and the head ache was horrendous. I wore an ice pack
> all morning. I sat on the couch for 2 hours and I started feeling a
> little better. I got up to use the rest room 50 feet away and began to
> cry by the time I got there, (any exertion made my head pain
> excruciating). My heart started pounding and I began shaking all over
> my entire body. If I did not know any better I would say I went into
> shock.
>
> Now I am no whine, never have been. Although I can tell you, that was
> freaky, and the pain was unbelievable, I was strangely calm in a weird
> sort of way. I really in all trueness with no exaggeration thought I
> was going to die with in a few moments. I decided to call my husband
> and say good bye. So I did. I told him this was the end of my fight
> with lyme, I did not believe I was going to live through this and
> please if he decided to come home not to drive fast cause I did not
> want him to die in an accident. I went out on the porch, I wanted to
> see the dogs and horses one last time, I stood there looking at the sky
> and told myself it was ok there was nothing I could to do, I had fought
> as long and hard as I could.
>
> My eldest lives next door (his dad had called him and told him to come
> over cause I was dieing) I am chuckling now as I am writing this down
> cause I am kind of embraced but it was not even funny while it was
> happening. My son got me some 02 and a coat because I was shaking all
> over and he talked with me and distracted me from the pain as he made
> me something to eat. I ate the little food and my hart quit pounding, I
> quit shivering and I lay there all bundled up an exhausted. I was out
> the rest of the day.
>
> Next day I woke up with the rotten beginnings of the headache again and
> wore an I pack all day around my neck. That went on till Monday
> afternoon (I am amazed that I don't have frost bite).
> On my symptom sheet I would have to say that my shoulder pain decreased
> by one to one and a half on the pain level. But that is all. That
> horrid headache is gone but my neck is still very stiff and my sinuses
> drip constantly, and my legs are still very heavy.
> I reported all this to Gary, he said that he would code for horror on
> the next session (among other things). You know I had a horrid (smile)
> child hood, so why did it surprise me that I would have emotional
> issues that would need to be addressed before I would be well again. It
> really is about treating the whole person isn't it?
>
> Lisa S in Washington State.
>