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> It seems though that it is very difficult to get it over to the

majority of chronically ill people that their illness could well have

been misdiagnosed originally, or that hypothyroid peep's who are

unable to get well because borrelia spirochetes are blocking their

receptor sites. They more than likely would test positive for

borreliosis. I sometimes wonder whether people have got so used to

suffering that they are reluctant to go down another path. All one

has to do is to type Lyme Disease into Google and take it from there.

>

> Luv - Sheila

Well, and people trust their doctors to think of and test for

everything...they don't realize doctors are human too, and sometimes

have their own opinions and " take " on things..their egos get in the

way at times, too....the internet has been such a great help to so

many, because now we're not powerless...( " encephalitis " was the word

I was thinking of..not meningitis....with that young guy they had

diagnosed with MS)..anyway..thank heavens they didn't give up and how

wonderful that your son has his life back...but terrible he had to

wait so long!

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> It seems though that it is very difficult to get it over to the

majority of chronically ill people that their illness could well have

been misdiagnosed originally, or that hypothyroid peep's who are

unable to get well because borrelia spirochetes are blocking their

receptor sites. They more than likely would test positive for

borreliosis. I sometimes wonder whether people have got so used to

suffering that they are reluctant to go down another path. All one

has to do is to type Lyme Disease into Google and take it from there.

>

> Luv - Sheila

Well, and people trust their doctors to think of and test for

everything...they don't realize doctors are human too, and sometimes

have their own opinions and " take " on things..their egos get in the

way at times, too....the internet has been such a great help to so

many, because now we're not powerless...( " encephalitis " was the word

I was thinking of..not meningitis....with that young guy they had

diagnosed with MS)..anyway..thank heavens they didn't give up and how

wonderful that your son has his life back...but terrible he had to

wait so long!

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> It seems though that it is very difficult to get it over to the

majority of chronically ill people that their illness could well have

been misdiagnosed originally, or that hypothyroid peep's who are

unable to get well because borrelia spirochetes are blocking their

receptor sites. They more than likely would test positive for

borreliosis. I sometimes wonder whether people have got so used to

suffering that they are reluctant to go down another path. All one

has to do is to type Lyme Disease into Google and take it from there.

>

> Luv - Sheila

Well, and people trust their doctors to think of and test for

everything...they don't realize doctors are human too, and sometimes

have their own opinions and " take " on things..their egos get in the

way at times, too....the internet has been such a great help to so

many, because now we're not powerless...( " encephalitis " was the word

I was thinking of..not meningitis....with that young guy they had

diagnosed with MS)..anyway..thank heavens they didn't give up and how

wonderful that your son has his life back...but terrible he had to

wait so long!

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HI Sheila, I have a friend who is suffering so badly. Knows he has lymes

disease, but cannot live a normal life. His wife emailed me yesterday...they

are taking out his gall bladder on Monday. They are at their wits end..he is in

so much pain all the time. He may have the same thing. Can you give me the

symptoms your son had? Explain more about this borreliosis? This may be the

answer for him!!

Thank you

PattiSue

Lyme Disease

Hi Diane,

This happened in my own family. My son has been ill for the past 27 years and

he was diagnosed with Guillan Barre Syndrome. He has been unable to work most

of this time and was never showed any signs that he would ever be well again.

This past year, I sent him to see a private specialist because I was so upset

at seeing him so ill and the NHS were failing him completely. As soon as he

started reeling off his symptoms, the specialist put up his hand and said " Stop

right there - I know what is the matter with you - you have borreliosis (LD) " .

Right there and then, he pricked my son's finger, placed a tiny drop of blood on

a slide, put it under his brand new darkfield video microscope and - walla!

there were the spirochetes. It took a little longer to find out more, but he was

absolutely right. He recollects being bitten by a tic on his ankle just inside

his right leg on the sock line, and every so often he gets a big rash in the

same place, even now, but he never knew what it was. My son had been

mis-diagnosed for all those years. He is now - like myself who also tested

positive for borreliosis - feeling well for the first time in 27 years. In fact,

when he began treatment, he sent me an e-mail saying " Mum - this is the first

day of my life! " - and it was. These past 2 months have almost been pain free

and his life has turned round 100%. I went to see this same specialist because

I was not getting better on the treatment for hypothyroidism, and I was also

found to be suffering from Lyme Disease. We are now both taking a form of Cat's

Claw - it is called Samento Extract and is very potent.

It seems though that it is very difficult to get it over to the majority of

chronically ill people that their illness could well have been misdiagnosed

originally, or that hypothyroid peep's who are unable to get well because

borrelia sp;irochetes are blocking their receptor sites. They more than likely

would test positive for borreliosis. I sometimes wonder whether people have got

so used to suffering that they are reluctant to go down another path. All one

has to do is to type Lyme Disease into Google and take it from there.

Luv - Sheila

Luv - Sheila

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