Isn't it strange... FM existed BEFORE Lyrica

[Guest guest]

Yeah. It has been around for years and years and people have treated us like

shit. So now that an approved drug has come along, they will just say it is a

money making scam and we are all still a bunch of nuts. There is no justice.

There is no way to ever explain this crap to anyone and have them believe it

unless they have it.

I am just ticked....................................

Oh well, better ease up before I get into a flare that won't let me function.

I love you all becuase we are in this together folks.

Debra V.

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

Never miss a thing. Make Yahoo your homepage.

[Guest guest]

If it works for me I don't care. When my son was dxed with ADHA one doctor told

me he had turetts syndrome and put a clonidyn patch on him. He truned into a

zombie. I found a new doctor and he pulled the patch off of him and gave me a

script for Ritilan. I was sad about the thought of putting him on the med. He

looked at me and said " a lot of children are medicated and do not need it. You

will know in one day if he needs this medication "

I filled the script and for the first time in his 7 years walking he sat at

the table for a complete dinner, he had a conversation with me with out running

in circles. He stopped repeating things after he said them the first time. He

could watch a complete movie like it was the first time he ever saw it. His

grades excelled in school.

WE only gave him meds while he was in school as time passed and by 15 he did

not want to take the meds anymore. That is another story.....Debi

debra van ness wrote:

Yeah. It has been around for years and years and people have treated

us like shit. So now that an approved drug has come along, they will just say it

is a money making scam and we are all still a bunch of nuts. There is no

justice. There is no way to ever explain this crap to anyone and have them

believe it unless they have it.

I am just ticked....................................

Oh well, better ease up before I get into a flare that won't let me function.

I love you all becuase we are in this together folks.

Debra V.

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

Never miss a thing. Make Yahoo your homepage.

[Guest guest]

-I sent an email to the author of the article in the NY Times, I am

sure like many, many sufferers that they were very upset. And I did

tell the author I would gladly trade places at any time with her. Now

the authors are going to try to cruify FM and chronic pain sufferers.

I think that we are punished enough with the doctors that look at you

like you fell off the hay wagon, what business is it if I want to pay

200 or whatever for the meds that I need, even if it makes me feel

better in my head the cost has been worth every penny. I know that

their are alot of people out there in alot more pain than myself but

it is real enough for me and I sure don't need some NY B***h telling

me that I have all this pain in my head.......That my friends is BS!!

myalgia_Support_Group , debra van ness

wrote:

>

> Yeah. It has been around for years and years and people have

treated us like shit. So now that an approved drug has come along,

they will just say it is a money making scam and we are all still a

bunch of nuts. There is no justice. There is no way to ever explain

this crap to anyone and have them believe it unless they have it.

> I am just ticked....................................

> Oh well, better ease up before I get into a flare that won't let

me function.

> I love you all becuase we are in this together folks.

> Debra V.

>

>

> ---------------------------------

> Never miss a thing. Make Yahoo your homepage.

>

>