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I'll definitely be taking a look at it.

I just had surgery three days ago for polyps and so far so good. Still blocked a little though and not being able to blow my nose is driving me plus everyone else insane with the sniffling I'm sure.

So far I feel that much better, no more incredibly blocked feeling so I'm really keeping my fingers crossed.

The surgery was a breeze, the removal of the packaging was gross to say the least.

mboylebradley <mboylebradley@...> wrote:

Hi Everyone,I posted here some time ago with regard to LDN and Samters. Well, I took my obsession to a whole new level and wrote a book .. I am sorry if this sounds like a shamelss plug .. it is .. because I want the world to hear this story. The book is called Up the Creek with a Paddle .. subtitle .. Beat MS and Many Autoimmune Disorders with Low Dose Naltrexone (LDN). My friend with samters is mentioned .. she is still taking LDN and thinks it may be helping her .. time will tell. The book is available on amazon.com and barnesandnoble.com and some local bookstores in Bergen County, NJ ... My website is very basic .. still working on it .. marybradleybooks.com ...All the Best Send instant messages to your online friends http://au.messenger.

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  • 3 years later...
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Hi ie,This site will tell you where and how to obtain Low Dose Naltrexone:http://tinyurl.com/how-to-obtain-ldnFor additional information about LDN, visithttp://tinyurl.com/intro-to-ldnWith best wishes,Dudley Delany

dudley_delanyFrom: ie

Sent: Monday, May 11, 2009 2:19 AM

Subject: RE.LDN

How can my daughter and I obtain a physician's prescription in Minnesota? Is this medication given only by certain physicians? Any info will be greatly appreciated.

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my wife take ldn for AS but when hashimoto was discovered it was said that it

was suppresed.

you can join the group and study the subject.ldn is a very amazing treatment

here is another message from the group for ldn

Hi Shayla,

I am no expert, but here's my story....I have Hashi's and so far have had some

good success with LDN.

I started with a dosage of 1.5mg and did not reduce the amount of thyroid meds I

was taking. It has been 5 weeks and I am definitely seeing improvements,

especially in the area of energy and inflammation.

Please email me privately if I can help you.

Amy

>

> Ok, I've missed posts on this LDN drug and autoimmune diseases. Now I read

this about Hashimoto's and this drug!

>

> " Those patients who are taking thyroid hormone replacement for a diagnosis of

Hashimoto’s thyroiditis with hypothyroidism ought to begin LDN at the lowest

range (1.5mg for an adult). Be aware that LDN may lead to a prompt decrease in

the autoimmune disorder, which then may require a rapid reduction in the dose of

thyroid hormone replacement in order to avoid symptoms of hyperthyroidism. "

> http://www.low dose naltrexone.org/#Cautionary_warnings

>

> Has anyone tried this? This would be amazing if it were true.

>

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  • 1 month later...
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I'm on LDN for Ulcerative Colitis and just get it from the GP. The chemist

order it in from dales.

>

> Hi Marg here

>

> I have a pal who has progressive MS and has been researching LDN.Can anyone

tell me where she can but it or a web address as she is really keen.I think I

read here a couple of people are taking it.

>

> Cheers folks.xxxxx

>  

> Margaret  

>

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If your friend joins the LDN usaer group below the facilitator will be able to

advise names of doctors who prescribe.

It can be obtained from skips pharmacy in florida with script and she needs to

under the supervision of a doctor

:LDN_Users/

jennyF

>

> Hi Marg here

>

> I have a pal who has progressive MS and has been researching LDN.Can anyone

tell me where she can but it or a web address as she is really keen.I think I

read here a couple of people are taking it.

>

> Cheers folks.xxxxx

>  

> Margaret  

>

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Margaret, go to the FILES section on our forum web site and

click on the FOLDER for LDN - the information you require is all in there.

Luv - Sheila

I have a pal who has progressive

MS and has been researching LDN.Can anyone tell me where she can but it or a

web address as she is really keen.I think I read here a couple of people are

taking it.

Cheers folks.xxxxx

Margaret

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How are you doing on it ?

Luv - Sheila

I'm on LDN for Ulcerative Colitis and just get

it from the GP. The chemist order it in from dales.

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Here is another reply for you me

Margaret Harrickey

From: freeman9007 <freemangoldcoast@...>thyroid treatment Sent: Tuesday, 7 July, 2009 17:29:42Subject: Re: LDNIf your friend joins the LDN usaer group below the facilitator will be able to advise names of doctors who prescribe.It can be obtained from skips pharmacy in florida with script and she needs to under the supervision of a doctor:LDN_Users/jennyF>> Hi Marg here> > I have a pal who has progressive MS and has been researching LDN.Can anyone tell me where she can buy it or a web address as she is really keen.I think I

read here a couple of people are taking it.> > Cheers folks.xxxxx> > Margaret >------------------------------------TPA is not medically qualified. Consult with a qualified medical practitioner before changing medication.

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  • 4 weeks later...
  • 1 year later...

This is offtopic so I'm just going to post the link for the LDN discussion

group again:

low dose naltrexone/

And the official LDN info site:

www.ldninfo.org

And the answer is yes, it's a pharma drug, and people get it prescribed.

However, it also can be purchased online w/o a scrip. I am sending you

info privately, .

People who are interested really should join the group and read the

website. It's very clear.

--

>Is this a product which needs a prescription?

>

>

>

>

~~~ There is no way to peace; peace is the way ~~~~

--A.J. Muste

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From: Baker <vbaker@...>iodine Sent: Tue, October 19, 2010 6:03:16 AMSubject: Re: LDN

This is offtopic so I'm just going to post the link for the LDN discussion

group again:

low dose naltrexone/

And the official LDN info site:

www.ldninfo.org

And the answer is yes, it's a pharma drug, and people get it prescribed.

However, it also can be purchased online w/o a scrip. I am sending you

info privately, .

People who are interested really should join the group and read the

website. It's very clear.

--

>Is this a product which needs a prescription?

>

>

>

>

~~~ There is no way to peace; peace is the way ~~~~

--A.J. Muste

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CharleyDidn't realize that you actually started treatment. How many weeks in now?? Your ALT and AST won't really matter much, as long as they are not wildly out to lunch. Now is the time for the viral loads especially; but, even the other readings they take for our blood work.Just like you, it only took one good fall for me to become very careful. Actually, I had several of those no reason falls and didn't think my knees were going to make it through tx. However, the worst was falling out of bed!! There is nothing sadder than an overweight middle age woman waking up to find herself on the floor between the bed and the closet. Worst part though - I Fell and I Can't Get

Up!!! But, I refused to ask for help getting back into bed at 3:00 am...Gloria

I think the first time I heard about Vertex was from Pam. I've had my hopes like every one else and now I don't believe any thing from them. For LDN IT did put my blood work where it should be butt my doctor wanted to to quit it. I had trouble sleeping but thats nothing new for me but not enough when your sick and need your rest. I think LDN might be good but I'm not smart enough to judge it. My first shot I thought I was going to die and but it doesn't bother me now I give myself the shots and even with a RN here and my son is in charge on my meds but won't give me shout but I would hide from getting shots in the Army and go back and get the medic to sign my shot record I'm alive but week and afraid I'm going to fall or let my sisters pup trip me. I'm sure I can make it through the meds

if my doctor and blood work are good. I wish I could say use the LDN but I couldn't say one way or the other my viral load went up to allmoast 20 Million and that was scary. My AST and ALT are off a little not sure about my Viral load but will be getting blood work on Monday.CharleyDo something while you can and don't be the coward I have been Sometime you just have to get mad as hell go into battle. I' m from Detroit but live in Tenn but plan to move back.My doctor isn't forign and speaks great english so that helps a lot too.

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  • 5 months later...
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My doctor prescribed it for me after I asked and refered him to the LDN website.  He said " well it can't hurt you.I really appreciated him giving me a modicum of credit for brains,  At first I got it from my PCP,.  Now my Neuro prescribes i to patients who ask.  I have MS and also take Copaxone.

I would love to have an FDA approved study done but I am counting on it found to be effective.I'd still take it even if not

Larry

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I wish more doctors would think like this... well it can't hurt you... I mean, really!On Sun, Apr 3, 2011 at 10:44 PM, Larry Stahl <larry@...> wrote:

My doctor prescribed it for me after I asked and refered him to the LDN website.  He said " well it can't hurt you.I really appreciated him giving me a modicum of credit for brains,  At first I got it from my PCP,.  Now my Neuro prescribes i to patients who ask.  I have MS and also take Copaxone.

I would love to have an FDA approved study done but I am counting on it found to be effective.I'd still take it even if not

Larry

-- Toni------Mind like a steel trap...Rusty and illegal in 37 states.

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Is there anyone else out there with MS who is taking LDN and Copaxone? My wife and I weren't sure if you can mix the two. So when she started the LDN we stopped the Copaxone.

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