Re: We live in Toronto and Husband's neuro won't prescribe LDN

[Guest guest]

i'm from ottawa just go to your family doc but you

will have to print out the ldn page to shaow that it

is fda aproved and the strenghts

--- mugsinto <mugsinto@...> wrote:

---------------------------------

My H has PPMS - walks with a cane and stil goes to

work. Has has it

since '95 but is very slow progessing.

We've just been told that his neuro doesn't prescribe

LDN because of

lack of clinical trials etc. Anybody have any

suggestions as to where

we go from here?

thanks

[Guest guest]

I get my Naltrexone from WWW.MEDSMEX.COM. $116 for 311, 4.5mg doses, 28, 50mg tabs. No RX necessary. You must dissolve each 50mg tab in 50ml of distilled water and use a baby dropper with ml. markings to take your needed dosage amount. This is how I bypassed my docs. I've been on it for 1 week with only slight improvement and no negative side effects. I'm taking 3mg (3ml) each night and will move to 4mg next week. Medsmex sells a quality product. The filler they use is lactose. Any questions? Good Luck. Screw your neuro and put your H's care into his own hands. Ed PS: There are plenty of clinical trials with 50mg doses for alchoholics and heroin addicts taking up to 3 50mg doses per day. NO ONE DIED! How will 3 - 4.5mg hurt you unless you are allergic to it. Does your husband have any drug allergies?mugsinto

<mugsinto@...> wrote: My H has PPMS - walks with a cane and stil goes to work. Has has it since '95 but is very slow progessing.We've just been told that his neuro doesn't prescribe LDN because of lack of clinical trials etc. Anybody have any suggestions as to where we go from here?thanks

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[Guest guest]

> My H has PPMS - walks with a cane and stil goes to work. Has has

it

> since '95 but is very slow progessing.

>

> We've just been told that his neuro doesn't prescribe LDN because

of

> lack of clinical trials etc. Anybody have any suggestions as to

where

> we go from here?

>

> thanks

>

>

>

>

>

>

>

[Guest guest]

Try 's Pharmacy at Yonge and Lawrence. I get liquid LDN there for my mom. The pharmacist will be able to give you a list of prescribing doctors. Sorry but I can't give out our doctor's name without his permission, but I will ask the next time we see him (next week.) Good luck!mugsinto <mugsinto@...> wrote: My H has PPMS - walks with a cane and stil goes to work. Has has it since '95 but is very slow progessing.We've just been told that his neuro doesn't prescribe LDN because of lack of clinical trials etc. Anybody have any suggestions as to where we go from here?thanks

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[Guest guest]

My husband was also diagnosed with PPMS last year. He started on LDN

in July and feels his walking is better when he doesn't forget to

take it. Someone on this group posted a message stating they went to

St. Mike's MS clinic and saw a Dr. Austin who gave them a script for

LDN. As a suggestion try 3 mgs or get the pills compounded at 3 and

1.5. My husband has tried 4.5 twice and finds that his legs are too

stiff. We live in the west end and get our LDN compounded (with

avicil) at the Medicine Shoppe on Bloor near Royal York. They are

very good. Best of luck. Louise

My H has PPMS - walks with a cane

and stil goes to work. Has has it

> since '95 but is very slow progessing.

>

> We've just been told that his neuro doesn't prescribe LDN because

of

> lack of clinical trials etc. Anybody have any suggestions as to

where

> we go from here?

>

> thanks

>

>

>

>

>

>

>

[Guest guest]

I got my Rx from Dr. Burton (neuro) at St Mikes and she is more than

willing to prescibe it to anyone who asks. She also pres. it to my

brother who has RRMS. I live in the North end of the city and get

mine filled at the Medicine Shoppe on Elgin Mills & Bayview. I

first started with liquid LDN 2 month supply costs $120.00 but now

take pill form with acidophilus filler 2 month supply costs $150.00

My H has PPMS - walks with a cane

> and stil goes to work. Has has it

> > since '95 but is very slow progessing.

> >

> > We've just been told that his neuro doesn't prescribe LDN

because

> of

> > lack of clinical trials etc. Anybody have any suggestions as to

> where

> > we go from here?

> >

> > thanks

> >

> >

> >

> >

> >

> >

> >