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Thank you ~ LDNers

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Dear LDNers,

Just a quick note to thank you for all of your good info and support

help in providing Hope, Inspiration, and methods of persuading Neuros

and MDs to prescribe LDN for MS patients. Also for recommending other

methods of assisting ourselves . After my experience today with my

Primary Care Physician, I am going to wait until mid~ January (when

my next apt is) with my Neuro who was not willing to prescribe the

two previous times I asked him. I'll try to push LDN again at that

time. I truly respect those of you who have been more successful than

I at securing a Rx.

In the meantime, thanks to info obtained via your group, I am making

and using a lot of Colloidal Silver, have stopped smoking, am taking

more vitamins and supplements, and increasing exercise. This will

allow me a little time to access the impact of these new therapeutic

changes. Come January, I'll be back. for any new ammunition to level

at my Neuro. If I can't get some, I'll use Medimex, or see if

someone else in the Portland / Vancouver/ or Olympia area has a Dr

that has materialized. LOL

My PCP was very conscientious, actually apologizing for her

reluctance to go outside of the recognized, accepted medical

parameters because of concern for her own medical license. A signed

release of responsibility was inadequate for her clinic. Morally, I

could not put my personal hope above her genuine concern for myself

and so many other patients. As MSers, we know about stress and

hopefully we are learning not to inflect ours onto others who are

doing the best that they can too.

I have gained so much from interacting with so many of you. Thanks:)

In fairness to myself, I will not be reading all of your group posts

for a while, but I am glad that you support each other so

affectionately. Keep up the good work. May God bless you, each one,

over the holidays!

Russ Miles :))~Vancouver, WA

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God Bless you too Russ!

Kathy

On 23-Nov-04, at 2:56 PM, Russ Miles wrote:

>

> Dear LDNers,

>

> Just a quick note to thank you for all of your good info and support

> help in providing Hope, Inspiration, and methods of persuading Neuros

> and MDs to prescribe LDN for MS patients. Also for recommending other

> methods of assisting ourselves . After my experience today with my

> Primary Care Physician, I am going to wait until mid~ January (when

> my next apt is) with my Neuro who was not willing to prescribe the

> two previous times I asked him. I'll try to push LDN again at that

> time. I truly respect those of you who have been more successful than

> I at securing a Rx.

>

> In the meantime, thanks to info obtained via your group, I am making

> and using a lot of Colloidal Silver, have stopped smoking, am taking

> more vitamins and supplements, and increasing exercise. This will

> allow me a little time to access the impact of these new therapeutic

> changes. Come January, I'll be back. for any new ammunition to level

> at my Neuro.  If I can't get some, I'll use Medimex, or see if

> someone else in the Portland / Vancouver/ or Olympia area has a Dr

> that has materialized. LOL

>

> My PCP was very conscientious, actually apologizing for her

> reluctance to go outside of the recognized, accepted medical

> parameters because of concern for her own medical license. A signed

> release of responsibility was inadequate for her clinic. Morally, I

> could not put my personal hope above her genuine concern for myself

> and so many other patients. As MSers, we know about stress and

> hopefully we are learning not to inflect ours onto others who are

> doing the best that they can too.

>

> I have gained so much from interacting with so many of you. Thanks:)

>

> In fairness to myself, I will not be reading all of your group posts

> for a while, but I am glad that you support each other so

> affectionately.  Keep up the good work. May God bless you, each one,

> over the holidays!

>

> Russ Miles :))~Vancouver, WA

>

>

>

>

>

>

>

>

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