Re: Adverse reactions to LDN Anyone? Wayne

[Guest guest]

I'm in South Australia.

What do you suggest compounding pharmacies mix with the Naltrexone

when making up capsules for the super-sensitive? I started on just

less than the usual dose. I thought it was safer for me to err on

getting less rather than too much. I am petite, and super-sensitive to

meds, so it made sense that I would need less than the average person.

I continued to have very unpleasant symptoms even when I reduced to

around 1.5 mg.

Thanks.

> > > Jan,

> > >

> > > I am not sure what CFS & MCS are, but you are right that if we

> > could figure

> > > out why you reacted this way to LDN, it might help many

people.

> > I, too, would

> > > have thought that you would have felt better. My question is

> > this; did you

> > > have none of these symptoms before starting LDN?

> > >

> > > Best of luck to you!

> > >

> > > Marcie

> > >

> > >

> > > In a message dated 10/18/2004 8:44:51 PM Central Daylight Time,

> > > atranceformer@y... writes:

> > >

> > >

> > > > I have CFS, MCS and am extremely sensitive to meds and many

> > foods.

> > > > I tried LDN recently but had such severe reactions to it

that I

> > had

> > > > to stop. Persisting for 2 weeks and then reducing the low

dose

> > by

> > > > half did not help enough for me to endure the treatment. My

> > > > reactions included, asthma (hadn't had any asthma for about a

> > year

> > > > before this), sore flaking skin, dramatically increased

fatigue

> > and

> > > > balance problems, worsened headache and my cognitive problems

> > were

> > > > much worse. This surprised me because after reading

everyone's

> > > > testimonials, I expected to feel better. I have since

heard of

> > only

> > > > one other person who had almost identical symptoms from

LDN, but

> > > > thought it worth posting here, in an effort to find out more.

> > > >

> > > >

> >

> >

> >

> >

> >