Tuesday, 20 August 2013

Weight gain & Lyme part two

Hello all,

Today is a momentous day for me, I was finally able to fit into a pair of jeans!

Two years....

After two years of treating the Lyme/spirochete infections and having an extreme weight fluctuation from putting on a lot to loosing a lot it seems the weight fluctuation has now stopped and the swelling has ceased.

I have spent two years observing other people who are able to wear jeans with ease but for me this was not the case at all.

In a way I was quite envious but I knew deep in my heart of hearts after talking to others who had been taking antibiotics for five years or more yes the weight does stabilize and once one is clear of any infection the weight goes back to normal.


I am so happy I am getting back to a normal weight and I am able to wear normal clothes like every one else.
Before I would try to put on some nice shoes and because of the swelling I would be crippled in pain and agony I would not be able to put any sort of shoe on other than trainers.

Today I was able to put on a pair of shoes other than trainers as well!

Keep Going...

All I can say is I shall keep on treating myself with MMS and going to Oxygen therapy I cannot say for how long but I shall keep updating.
Keep going with whatever treatment you have chosen to do it is worth it really it is.

Yes this is a momentous day for me that is for sure.

Here is the link to part 1 of weight gain & Lyme:
Lyme Girl x


 **Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.**

 Copyright 2012-2013  LymeGirl all rights reserved.

Sunday, 11 August 2013

Stomach / GI problems and Lyme/Spirochete Infection

Hello all,

I thought I would look at Stomach/Gastrointestinal problems and Lyme/Spirochete infections.

Kick in the stomach


Lyme/Spirochete infections will/can  affect every organ in the body so I have found out from my own and

family members experience and my own research on the subject.

I have had my appendix removed because of Lyme/Spirochete infections.

My brother had to go on a specialized diet due to Spirochete infection (not that anyone knew at the time the cause of his stomach problems).

The doctors wanted to remove my gall bladder and my spleen (they did not thank goodness).

Yes the wonderful infections not only affect the brain, eyes, ears, throat but also it gets one in the stomach!

My stomach problems

As I have mentioned I had my appendix removed about 2 years after the Horse fly bite.
Now whether or whether not my appendix was due to rumble at the time that it did I am now pretty certain
it may not have if I had not of been infected by the Horse fly.

The reason I come to this conclusion is because the Spirochete infection affects every organ in the body,
well it has in my body at least, so it would stand to reason the appendix would get inflamed.

Career Change....

When I was 20 I got my first managerial job, how i managed to pass my course I will never know
but I did it.

The job was extremely stressful well the Catering industry is. Long hours little time to eat a proper meal,
constantly on your feet.

It was inevitable I was going to have a burn out and sure enough I had the ultimate burn out.
My back gave in, I mean I could not move and with this my stomach started to have extreme pain in my
stomach and I had a terrible heartburn feeling.

The Dr advised I should have a white food diet i.e. White rice, white fish, Chicken.
This was when I was told I had an ulcer and a problem with my spleen and gall bladder and they or one may have to be removed!
Funny how all of a sudden out of the blue my body started to fall apart from just my first job as a manager.
 The Doctor advised the job i was doing was too stressful and highly dangerous for me.

I had spent years studying at collage and acquired debts with being a student and then I was told i had
 chosen the wrong career all because my stomach and GI were not coping.

Needless to say i went down the homoeopathic route and yes gave up my career as a Hotel manager.
I did not have my spleen removed or Gall bladder either.

While Pregnant.....

When I was pregnant I suffered from terrible heartburn and reflux I drank bottle after bottle of antacid I was told "Oh quite normal, many pregnant women suffer from this"
I wonder now if a lot of my problems during my pregnancy were actually made worse than most due to the Spirochete infection i would say now Categorically yes.

During treatment......

I have suffered from bloating in the stomach while treating with MMS but if I had taken antibiotics this would also happen so MMS is not to blame.
I have also had really bad reflux and indigestion while treating and again this could happen if one is on antibiotics neither are to blame only the spirochete infection is to blame.
I am glad to say that this part has seemed to have calmed down quite a lot.

My Motto

My motto is when dealing with the heartburn or stomach problems is to:
Just eat plenty of Yogurt and bananas cut out processed foods and sugar and drink lots of water until acid burning subsides. I find Cranberry juice helps immensely and Acidophiles and manage my stress levels with yoga as Lyme loves it when we are stressed and not at our best.

I would suggest if one is suffering with a GI problem bear this in mind the infection does cause inflammation and if one is taking treatment like MMS or antibiotics it does seem to be all part of the process of ridding the infection.

Good Luck

Lyme Girl x

Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.**

 Copyright 2012-2013  LymeGirl all rights reserved.

Sunshine,Heat & Lyme Part two

Hello all,

I have not written for a little while because I have been outside enjoying the beautiful sunny weather here in the UK.

I have been sitting in the sun mainly for medicinal purposes really of course I have not been sitting in the sun for extensive periods of time and never in the midday sun.


Has it helped me?

Yes the sun has really helped me health wise and mood wise too.

I used to get a tingling sensation when I went into the sun or a sauna or a hot bath and in the past because i did not know the truth about M.S. and Spirochete infection I would automatically assume it was an M.S attack.

Before I was diagnosed with M.S I used to think there was something wrong with me or it was psychological or that was what I was told by the Dr's etc.

They can run, they are scared, they are cowards those Spirochetes

Now I am aware of what was wrong with my body I realize the tingling is not an M.S attack at all but a  reaction from the spirochetes trying to escape or dying off because they hate the heat they hate the sun.

When I used to get the tingling I would immediately get out of the heat or sun and go into the shade exactly what the little blighters wanted!

I have already written about sunshine and Lyme before here :

I do know most people with autioimmune diseases or other conditions do get adversly affected by heat and sun and it is always wise to be careful I would suggest to do what one feels one can cope with.

I also feel that if one is actually treating any condition that is actually related to Lyme?Spirochete infection, treating with MMS or antibiotics well the person is on their way to being cured and can maybe tolerate heat and the sun better than before.

I do know that with some antibiotics one has to stay out of the sun so always consult your LLMD and consult the instructions for any medication.

That is the beuaty of MMS you can go into the sun while taking MMS and there are no adverse reactions.

I personally grit my teeth and ignore the tingiling and itching, in my mind I can see the little blighters shriveling up and dying once and for all!

I refuse to rush to the shade like a bat because that is what they want no tough make me tingle make me itch they will not win!

Now since treating with MMS the tingling and itching is nothing like it used to be not at all now it is fleeting if at all, I feel happy in the knowledge that I won and they did not and now can enjoy a sauna or a sit in the sun with more ease not discomfort.

I now say this to all who do suffer in the sun and the heat try to grit your teeth perhaps when the itching starts before diving for cover.


Walking through sand.....

Yes in the heat I found it harder to walk I felt like I was walking through sand my legs were really hard to lift
and my knees used to not be able to bend with ease,

my ankles would ache and throb or my shins would ache and throb or i would get stabbing pains or electric shock sensations all over my body or my scalp.

This was when I would go in the sun before treatment with MMS  and now after treatment with MMS

I am happy to report that these problems do not occur!

The sun has got his hat on Hip Hip Hippo ray!

So hopefully as long as our UK summer lasts I shall keep on with my daily routine of getting outside whenever the sun has got his hat on!

Good Luck

Lyme Girl x

 *Always consult a LLMD (Lyme Literate Doctor) or your own health care professional.**

 Copyright 2012-2013  LymeGirl all rights reserved.