Neuron problems

[Guest guest]

Hi Lynette,

I'm beginning to suspect heavy metals in neuron anything, from Parkinson's

etc. Did you by any chance, get a heavy metals test (arsenic, aluminum,

lead, asbestos, mercury or barium)?

I had three Uncles who welded most anything, worked with asbestos and many

other metals and one is dead (died of cancer, and shaking to pieces),

another is dying with cancer and Mesothelioma and the third has bad shaking

problems in his right hand, when he moves it (said to not be Parkinson's).

My third Uncle asked for LDN from his Veteran's doctor, and in the

beginning, he was promised he would be prescribed LDN if he tried the slew

of prescriptions first, but then his doctor flatly refused when nothing

helped him. His doctor said he needed to see a Neurologist for heavy metals

and that doctor 'might' prescribe LDN for him.

In the meantime, they have my third Uncle on the 'prescription treadmill',

overdosing him with blood pressure prescriptions to the point where he would

pass out and fall onto a concrete floor. One time he was so bruised and

cut, his brother was shocked beyond belief. My Uncle finally had to cut his

dose of blood pressure pills down by half and then half again, to keep from

passing out. Criminal activity going on here by the 'doctors'!

I think something that will chelate heavy metals from my Uncle's body might

be the best route. Not sure if that would be Zeolite or something else. He

desperately needs help that he isn't getting from the pharma doctors!

Thank you,

Jean

*******************

> From: Lynnette <amberlyn@...>

> Date: Sun, 20 Feb 2011 21:12:13 -0000

> <low dose naltrexone >

> Subject: [low dose naltrexone] New Here, with questions

>

> Hello -

>

> First a bit of background. I am female, retired, on BHRT (no ovaries),

> Thyroid-S 6.5 grains(no thyroid), and hydrocortisone 27.5mg for my worn-out

> adrenals. I take 50mg Iodoral, and other nutrients to support my being

> thyroidless...

>

> This past year, I noticed a loss of strength in my right hand, followed by

> muscle wasting and clawing tendencies in the fingers. The neurologist gave me

> a long laundry list of possible diseases. None were nice. I researched the

> lot, and if anything, I might have a motor neuron disease. Might. The blood

> lab indicated no autoimmune problems... ANA neg... and in fact, nothing was

> out of range.

>

> I started LDN 1.5mg one week ago, to stall whatever it is. I am scheduled to

> increase my dose to 3mg tomorrow.

>

> Prior to starting LDN, I had managed to get my hormones in balance, and was

> sleeping well. With LDN, the night sweats have returned. Is this normal? Will

> they go away with continued use?

>

> At any rate, the LDN is my first non-hormone Rx. Given my situation, can I

> expect it to be of benefit to me?

>

> Thanks!

> Lynnette

>

>

>

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>