Re: ldn use for MS---in the 1st few weeks noticeable changes

[Guest guest]

Thanks Cath,

I watched my husband turn completely around.

Aletha

[low dose naltrexone] ldn use for MS---in the 1st few weeks

noticeable changes

>I have been looking into ldn for my early stages of ALS, so I have

> been a member here for a little bit. I am friends with

> (pomsaregreat) who posts here and has MS, and I wanted to mention

> something regarding her starting the ldn.

>

> She has only been on it for a few weeks, and already I notice when

> we talk on the phone she seems to have more energy and less

> cognitive difficulty. I admit to having been fairly skeptical at

> times on whether or not ldn works, but I can say that without a

> doubt it seems to be helping her. (I hope I haven't embarassed you

> too much, !)

>

> The reason I mention it is because if anyone out there with MS is

> sitting on the fence regarding taking it, I certainly would

> encourage them to at least give it a try. If it makes such a

> noticeable difference from another persons perspective (who admits

> she expected the ldn not to change the symptoms much), I can only

> imagine how well it's working. So please go ahead and give it a

> shot!

>

> Sometimes I love being wrong!

>

> Sincerely,

>

> Cath

>

>

>

>

>

>

>

>

[Guest guest]

Awwwww Cath you would never embarrass me. In fact I appreciate your

input. It's harder for a person who has the disease to notice

differences in themselves. I find that given the ups and downs with

ms sometimes the changes are too subtle for me to notice. Sometimes

I need a mack truck bearing a sign its working to hit me square in

the face ;op

I have to admit tho I have noticed my cognitive problems and energy

getting better. I can actually use my brain later in the day ;o0

I'm actually able to accomplish abit more energy wise.

Now! On to you! I hope you can get a script soon! I know this is

going to help you Cath! I won't take no for an answer! No ifs,ands

or buts its going to halt your progression! If I have to drive some

down there I will )

Hugs

>

> I have been looking into ldn for my early stages of ALS, so I have

> been a member here for a little bit. I am friends with

> (pomsaregreat) who posts here and has MS, and I wanted to mention

> something regarding her starting the ldn.

>

> She has only been on it for a few weeks, and already I notice when

> we talk on the phone she seems to have more energy and less

> cognitive difficulty. I admit to having been fairly skeptical at

> times on whether or not ldn works, but I can say that without a

> doubt it seems to be helping her. (I hope I haven't embarassed you

> too much, !)

>

>

[Guest guest]

,

I sure am hoping to get a script as well. My internist is looking

into the ldn, and in the past he has been very open minded, so I feel

like I have a decent chance he'll order it. Thanks for the

encouragement!

Hugs, Cath

--- In low dose naltrexone , " " <pomsaregreat@y...>

wrote:

>>

> Now! On to you! I hope you can get a script soon! I know this is

> going to help you Cath! I won't take no for an answer! No ifs,ands

> or buts its going to halt your progression! If I have to drive some

> down there I will )

>

> Hugs

>

[Guest guest]

Fingers crossed. Toes crossed. Eyes crossed. Legs crossed and

hmmmm.......anything else I can cross? Lol!

If internist doesn't prescribe it then we look for a new doc. here.

Not gonna give up easy!!!

Bigs hugs

> ,

>

> I sure am hoping to get a script as well. My internist is looking

> into the ldn, and in the past he has been very open minded, so I feel

> like I have a decent chance he'll order it.