Re: Re: ldn without Dr. How does that work?

[Guest guest]

Or go ahead and continue to be afraid but STILL take control... fear is pretty much a part of the MonSter's presence. You certainly have no obligation to your doctor, who is supposed to be helping you, not hindering your efforts to find improvement and stability.

JT

----- Original Message -----

From: Cinders

low dose naltrexone

Sent: Thursday, July 15, 2004 11:39 AM

Subject: [low dose naltrexone] Re: ldn without Dr. How does that work?

Jeanie - question for you. The doctor who is "watching over you" right now is doing what - watching you get worse? You say you feel bad, that you feel the MS attacking (and I know EXACTLY what you mean because I could feel it too) that you feel like crap. So - it's time to try something new. If your doctor says No, like mine did, like so many do - who cares???? You are an adult. It is your life, your body, your choice. You are the one that goes home and deals with the MonSter. Not your doctor. Stop being afraid and take control. And don't tell your Neuro your taking LDN if you don't want to. He's not going to know unless you decide to share the information.

[Guest guest]

We do tend to forget that our doctors work for us, not the other way around.

----- Original Message -----

From: Johanne F

low dose naltrexone

Sent: Thursday, July 15, 2004 1:27 PM

Subject: [low dose naltrexone] Re: ldn without Dr. How does that work?

.. My Dr said no to > ldn and if I go against him who will watch over me? The first time I saw my neuro, he told me I have MS. When he told me he only had drugs to help with the symptomes (the CRABS weren't out yet). I told him," ok, so do you know of or have any patients doing beetings?" He wasn't sure but he gave me the info to contact town university (they were starting a study on beestings for MS).So I told him that I'd like him to be my neuro and watch me try differnet things. He said ok.Now he does research for MS and he knows many of the reseachers around the world. So basically he keeps me up to date on the possible studies that I could try and I keep him up to date on whatever therapy I'm doing.There are no problems. No, he didn't write the perscrition for LDN I got it from a GP.Just get the LDN and tell your neuro to watch you. Don't forget you are the one who is consulting him and you can chose anyone you want.

[Guest guest]

A big Right On to this message!

----- Original Message -----

From: " Cinders " <allentownusa@...>

<low dose naltrexone >

Sent: Thursday, July 15, 2004 11:39 AM

Subject: [low dose naltrexone] Re: ldn without Dr. How does that work?

> Jeanie - question for you. The doctor who is " watching over you "

> right now is doing what - watching you get worse?

>

> You say you feel bad, that you feel the MS attacking (and I know

> EXACTLY what you mean because I could feel it too) that you feel

> like crap.

>

> So - it's time to try something new. If your doctor says No, like

> mine did, like so many do - who cares???? You are an adult. It is

> your life, your body, your choice. You are the one that goes home

> and deals with the MonSter. Not your doctor. Stop being afraid and

> take control. And don't tell your Neuro your taking LDN if you don't

> want to. He's not going to know unless you decide to share the

> information.

>

> LDN is not going to make you worse. The possible side effects are

> minor for most, and seem to almost always go away pretty quick. LDN

> may not help - there are a few who feel it hasn't helped them, but

> it might help a whole lot. It did for me. Either find a doctor in

> your area who will give you a script, call one of the doctors who

> are frequenly listed as giving scripts over the phone, or buy some

> Revia from Medsmex and give LDN a try.

>

> JMHO - Cinders

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