Re: LDN for Lyme say what?

[Guest guest]

>

> Hi ,

>

I'm glad the LDN is working for you! How long did it take

> for your immune system to get regulated?

>

>

===========

I was one of the lucky one's and had symptom improvement overnight on

my first dose of LDN, I started at 4.5mg. I experiencd some quirky

side effects from the LDN for the first 6 months but I rode all of

them out. I think I realized that the progression switch had been

turned off about 4 months into my LDN treatment. I will probably

never know the cause of my compromised immune system at birth. I know

I was such a nightmare of an infant and no doctor had an answer for my

parents of why this or why that, that my mom swore she'd never have

another baby and she didn't. I do know I have been treated so heavily

with antibiotics over my life that I am eaten up with candida yeast

and I steadily work trying to battle it and keep it as low as I can.

[Guest guest]

All we will do here is if a person is having trouble with LDN failing

them we try and look at all possibilities of why and that can be

suggesting they get their yeast load checked, Dr. McCandless tells us

to look at our diet because our diet can conflict with LDN and you may

get unwanted side effects, there could be possible misdiagnosis. We

have seen well over 20 people on various LDN forums have an MS

diagnosis go on LDN and do poorly or have symptoms increase severely

that later found they were misdiagnosed and actually have lyme instead

so we suggest some get a lyme test through various labs or

microscopes. I love it when a person with MS or ALS finds he/she has

lyme instead of MS or ALS because lyme can be treated more

successfully.

Hope this helps some of you to understand why I push people to get

tested for this or that or look at this or that to see why LDN may not

be doing for you what it has done for so many others.

[Guest guest]

Don't ever change ! What made you take up this cause?

I have another question for you? If a person has the same symptoms

as I did on the LDN, would you think they also had Lyme?

That being mood swings rages and depression?

Thanks

>

>

> All we will do here is if a person is having trouble with LDN

failing

> them we try and look at all possibilities of why and that can be

> suggesting they get their yeast load checked, Dr. McCandless tells

us

> to look at our diet because our diet can conflict with LDN and you

may

> get unwanted side effects, there could be possible misdiagnosis.

We

> have seen well over 20 people on various LDN forums have an MS

> diagnosis go on LDN and do poorly or have symptoms increase

severely

> that later found they were misdiagnosed and actually have lyme

instead

> so we suggest some get a lyme test through various labs or

> microscopes. I love it when a person with MS or ALS finds he/she

has

> lyme instead of MS or ALS because lyme can be treated more

> successfully.

>

> Hope this helps some of you to understand why I push people to get

> tested for this or that or look at this or that to see why LDN may

not

> be doing for you what it has done for so many others.

>

>

>

[Guest guest]

>

> Don't ever change ! What made you take up this cause?

>

> I have another question for you? If a person has the same symptoms

> as I did on the LDN, would you think they also had Lyme?

> That being mood swings rages and depression?

>

> Thanks

===========

I want to see as many people suffering to get as much relief out of

LDN as I have.

I'd look at diet, possible yeast overgrowth and the possibility of

lyme.