Jump to content
RemedySpot.com

good news

Rate this topic


Guest guest

Recommended Posts

Guest guest

Hi all,

I bought all the copies of " Time " at HEB. I challenge all of you to do

the same. I love the picture on the front it's almost like he's dancing

with the wind. Have a great week. Trina

good news

I forwarded the Times article to an out of state friend who works as a

television producer. Her news director is considering doing an autism

piece

for sweeps this summer. It's not in Texas...but again, the media is

interested.

All television stations have websites these days and they do have a

story

suggestion boxes. The Time article is not a bad thing to submit...also

with

links to research methodology the Time article missed.

Just a thought.

Link to comment
Share on other sites

Guest guest

Trina,

I too made my husband buy all the copies of " Time " at the and

Noble in the Arboretum! Hehe.

Mache Liu

and Trina Sherman wrote:

> Hi all,

> I bought all the copies of " Time " at HEB. I challenge all of you to do

>

> the same. I love the picture on the front it's almost like he's

> dancing

> with the wind. Have a great week. Trina

>

> good news

>

> I forwarded the Times article to an out of state friend who works as a

>

> television producer. Her news director is considering doing an autism

>

> piece

> for sweeps this summer. It's not in Texas...but again, the media is

> interested.

>

> All television stations have websites these days and they do have a

> story

> suggestion boxes. The Time article is not a bad thing to

> submit...also

> with

> links to research methodology the Time article missed.

>

> Just a thought.

>

>

>

>

>

>

>

Link to comment
Share on other sites

Guest guest

What good does it do for parents of autistic children to hoard all the

copies of " Time " I thought the idea was to get the world at large

informed not keep it to ourselves!

Have I got the wrong outlook???????

Mache wrote:

> Trina,

> I too made my husband buy all the copies of " Time " at the and

> Noble in the Arboretum! Hehe.

> Mache Liu

>

> and Trina Sherman wrote:

>

> > Hi all,

> > I bought all the copies of " Time " at HEB. I challenge all of you to do

> >

> > the same. I love the picture on the front it's almost like he's

> > dancing

> > with the wind. Have a great week. Trina

> >

> > good news

> >

> > I forwarded the Times article to an out of state friend who works as a

> >

> > television producer. Her news director is considering doing an autism

> >

> > piece

> > for sweeps this summer. It's not in Texas...but again, the media is

> > interested.

> >

> > All television stations have websites these days and they do have a

> > story

> > suggestion boxes. The Time article is not a bad thing to

> > submit...also

> > with

> > links to research methodology the Time article missed.

> >

> > Just a thought.

> >

> >

> >

> >

> >

> >

> >

Link to comment
Share on other sites

Guest guest

I have to ask the same question....

It would make more sense to share the news with others rather than

keep it all to ourselves. Would it not?

~ :)

San

> What good does it do for parents of autistic children to hoard all

the

> copies of " Time " I thought the idea was to get the world at large

> informed not keep it to ourselves!

>

> Have I got the wrong outlook???????

Link to comment
Share on other sites

Guest guest

For your information, I kept one copy for myself and passed the rest out

to neigbors and coworkers. Is that okay with you?

Mache Liu

Bruce Jeffcoat wrote:

> What good does it do for parents of autistic children to hoard all

> the

> copies of " Time " I thought the idea was to get the world at large

> informed not keep it to ourselves!

>

> Have I got the wrong outlook???????

>

> Mache wrote:

>

> > Trina,

> > I too made my husband buy all the copies of " Time " at the

> and

> > Noble in the Arboretum! Hehe.

> > Mache Liu

> >

> > and Trina Sherman wrote:

> >

> > > Hi all,

> > > I bought all the copies of " Time " at HEB. I challenge all of you

> to do

> > >

> > > the same. I love the picture on the front it's almost like he's

> > > dancing

> > > with the wind. Have a great week. Trina

> > >

> > > good news

> > >

> > > I forwarded the Times article to an out of state friend who works

> as a

> > >

> > > television producer. Her news director is considering doing an

> autism

> > >

> > > piece

> > > for sweeps this summer. It's not in Texas...but again, the media

> is

> > > interested.

> > >

> > > All television stations have websites these days and they do have

> a

> > > story

> > > suggestion boxes. The Time article is not a bad thing to

> > > submit...also

> > > with

> > > links to research methodology the Time article missed.

> > >

> > > Just a thought.

> > >

> > >

> > >

> > >

> > >

> > >

> > >

Link to comment
Share on other sites

  • 2 years later...
Guest guest

Yeah, hi might have been surprised but then again,

THAT makes the win that much sweeter!!!!

--- Lucy Lefler wrote:

> Thank you one and all. Methinks the critter was

> surprised that I fought

> back. A toast ... to all the fighters ... sometimes

> we get lucky.

>

>

>

> At 02:12 PM 3/6/2005 +0000, you wrote:

>

>

> >Yipee so glad to hear this news. I'll take a Dragon

> Filet Mignon

> >with a baked potato with the works please with a

> shot of tequila.

> >

> >Fred

> >

> >

> >In a message dated 3/3/2005 10:01:21 PM Central

> Standard Time,

> >lu@... writes:

> >

> >Today my Drs office called .... (drum roll,

> please) ... and told me

> >the

> >virus is undetectable!!!!

> >SVR! SVR! For 6 more months, until the next

> test, I am free!!

> >

> >Dragon steak, anyone?

> >

> >

> >

> >Sweet!!

> >

> >

> >

> >

> >

> >

> >

> >It's a pleasure having you join in our

> conversations. We hope you have

> >found the support you need with us.

> >

> >If you are using email for your posts, for easy

> access to our group, just

> >click the link--

> http://groups.yahoo.com/group/Hepatitis_C_Central/

> >

> >Happy Posting

> >

Link to comment
Share on other sites

Guest guest

Luz,

Yippie on the Cero count.

Yo habla espanol muy piceto. LOL

But let me put it this way. Excellente!!!!

Love

Janet

Luz Ramos wrote:

>

> Yipee so glad to hear this news. I'll take a Dragon Filet Mignon

> with a baked potato with the works please with a shot of tequila.

>

> Fred

>

>

> In a message dated 3/3/2005 10:01:21 PM Central Standard Time,

> lu@s... writes:

>

> Today my Drs office called .... (drum roll, please) ... and told

me

> the

> virus is undetectable!!!!

> SVR! SVR! For 6 more months, until the next test, I am free!!

>

> Dragon steak, anyone?

>

>

>

> Sweet!!

Yeap I'm so happy doble too. Guess what Guys, last time I wrote was

in last nov. Then my doc put me in interferon and rivavirin. And

guess what???

After 4 months of therapy I'm out of the Moth...Fuck... dragon too.

My genotype is 4 and my doc tells me I have 50% but guess what I get

the winning number too, because this is like a lottery number. Well I

hope tells everyone who start therapy that don't give up. From today

I have the hope to tells all new people do the treatment no matter

what, you have the hope. Today I'm celebrate too with a Big piece of

Dragon a la B.B.Q. But I don't give up. Thanks for all yours guys,

I read everyday everything and I want to stay forever in this big

family. And I hope to stay in cero forever. Forgive for my english

but I'm spanish. Love alls yours

Luz Ramos

It's a pleasure having you join in our conversations. We hope you have found the

support you need with us.

If you are using email for your posts, for easy access to our group, just click

the link-- http://groups.yahoo.com/group/Hepatitis_C_Central/

Happy Posting

Link to comment
Share on other sites

Guest guest

Luz,

Bueno!! BUeno!! Bueno!! (How do you say Wonderful & Fantastic in Spanish?)

Glad to hear it!! BBQ Dragon sounds great!!

May you stay healthy!

At 01:43 AM 3/10/2005 +0000, you wrote:

>

> >

> > Yipee so glad to hear this news. I'll take a Dragon Filet Mignon

> > with a baked potato with the works please with a shot of tequila.

> >

> > Fred

> >

> >

> > In a message dated 3/3/2005 10:01:21 PM Central Standard Time,

> > lu@s... writes:

> >

> > Today my Drs office called .... (drum roll, please) ... and told

>me

> > the

> > virus is undetectable!!!!

> > SVR! SVR! For 6 more months, until the next test, I am free!!

> >

> > Dragon steak, anyone?

> >

> >

> >

> > Sweet!!

>

>Yeap I'm so happy doble too. Guess what Guys, last time I wrote was

>in last nov. Then my doc put me in interferon and rivavirin. And

>guess what???

>After 4 months of therapy I'm out of the Moth...Fuck... dragon too.

>My genotype is 4 and my doc tells me I have 50% but guess what I get

>the winning number too, because this is like a lottery number. Well I

>hope tells everyone who start therapy that don't give up. From today

>I have the hope to tells all new people do the treatment no matter

>what, you have the hope. Today I'm celebrate too with a Big piece of

>Dragon a la B.B.Q. But I don't give up. Thanks for all yours guys,

>I read everyday everything and I want to stay forever in this big

>family. And I hope to stay in cero forever. Forgive for my english

>but I'm spanish. Love alls yours

>

>Luz Ramos

>

>

>

>

>

>

>It's a pleasure having you join in our conversations. We hope you have

>found the support you need with us.

>

>If you are using email for your posts, for easy access to our group, just

>click the link-- http://groups.yahoo.com/group/Hepatitis_C_Central/

>

>Happy Posting

>

Link to comment
Share on other sites

Guest guest

Molzeltoff (spelling)

Fred

Luz,

Bueno!! BUeno!! Bueno!! (How do you say Wonderful & Fantastic in

Spanish?)

Glad to hear it!! BBQ Dragon sounds great!!

May you stay healthy!

At 01:43 AM 3/10/2005 +0000, you wrote:

>

> >

> > Yipee so glad to hear this news. I'll take a Dragon Filet Mignon

> > with a baked potato with the works please with a shot of tequila.

> >

> > Fred

> >

> >

> > In a message dated 3/3/2005 10:01:21 PM Central Standard Time,

> > lu@s... writes:

> >

> > Today my Drs office called .... (drum roll, please) ... and told

>me

> > the

> > virus is undetectable!!!!

> > SVR! SVR! For 6 more months, until the next test, I am free!!

> >

> > Dragon steak, anyone?

> >

> >

> >

> > Sweet!!

>

>Yeap I'm so happy doble too. Guess what Guys, last time I wrote was

>in last nov. Then my doc put me in interferon and rivavirin. And

>guess what???

>After 4 months of therapy I'm out of the Moth...Fuck... dragon too.

>My genotype is 4 and my doc tells me I have 50% but guess what I get

>the winning number too, because this is like a lottery number. Well

I

>hope tells everyone who start therapy that don't give up. From

today

>I have the hope to tells all new people do the treatment no matter

>what, you have the hope. Today I'm celebrate too with a Big piece

of

>Dragon a la B.B.Q. But I don't give up. Thanks for all yours guys,

>I read everyday everything and I want to stay forever in this big

>family. And I hope to stay in cero forever. Forgive for my

english

>but I'm spanish. Love alls yours

>

>Luz Ramos

Link to comment
Share on other sites

  • 3 months later...
Guest guest

Fan-dang-tastic! Congrats, Alan.

> I am sending this post in the hope that it will give

> those going thru treatment or considering it

> encouragement and positive vibes. I am a 52 year old

> male genotype 2b viral load was 18 million. I did

> combo treatment peg and riba for 24 weeks. Side

> effects of treatment were untolerable for me mentally

> untill I went on and antidepressant,(thanks Doug)

> physically were tough but tolerable and got easier as

> time went on especially once I decided to get more

> active and started excersing. I finsihed my treatment

> Nov.04 did my PCR test end of May 05 and got my

> results yesterday. Happy to say I have cleared the

> virus as it was undetectable in my system. (I know

> there might be miniscule amounts hiding in my organs

> but Im gonna look at the glass being half full and

> say Ive cleared and slayed the dragon.) Now I am

> praying that each and everyone of you will be blessed

> by God and slay your dragon. I will remember all of

> you in my prayers every evening (especially Janet who

> continues her corageous fight and still finds time to

> comfort the members of this group.) Dont ever give up,

> continue the fight,and were allgoing to slay the

> dragon. Thx and God Bless Alan

>

> __________________________________________________

>

Link to comment
Share on other sites

Guest guest

Alan, I *love* hearing stories like yours! Hope your SVR goes on forever!

Marilyn

Good News

I am sending this post in the hope that it will give

those going thru treatment or considering it

encouragement and positive vibes. I am a 52 year old

male genotype 2b viral load was 18 million. I did

combo treatment peg and riba for 24 weeks. Side

effects of treatment were untolerable for me mentally

untill I went on and antidepressant,(thanks Doug)

physically were tough but tolerable and got easier as

time went on especially once I decided to get more

active and started excersing. I finsihed my treatment

Nov.04 did my PCR test end of May 05 and got my

results yesterday. Happy to say I have cleared the

virus as it was undetectable in my system. (I know

there might be miniscule amounts hiding in my organs

but Im gonna look at the glass being half full and

say Ive cleared and slayed the dragon.) Now I am

praying that each and everyone of you will be blessed

by God and slay your dragon. I will remember all of

you in my prayers every evening (especially Janet who

continues her corageous fight and still finds time to

comfort the members of this group.) Dont ever give up,

continue the fight,and were allgoing to slay the

dragon. Thx and God Bless Alan

Link to comment
Share on other sites

  • 1 month later...

We all have our bd moments Pete......but right now it's time to

CELEBRATE!

To bad I can't put graphics......but imagine balloons and a sign with bright

colored letters that says.....

CONGRATULATIONS!!!!

Love,

Nursey

Link to comment
Share on other sites

We all have our bd moments Pete......but right now it's time to

CELEBRATE!

To bad I can't put graphics......but imagine balloons and a sign with bright

colored letters that says.....

CONGRATULATIONS!!!!

Love,

Nursey

Link to comment
Share on other sites

We all have our bd moments Pete......but right now it's time to

CELEBRATE!

To bad I can't put graphics......but imagine balloons and a sign with bright

colored letters that says.....

CONGRATULATIONS!!!!

Love,

Nursey

Link to comment
Share on other sites

Thats great news Pete. were you into stage 4 cirrhosis?. Did I

read that right? It was a Roche study using Shering drugs?

Stranger things can happen I guess. Happy for you.....your friend...ric

Link to comment
Share on other sites

Thats great news Pete. were you into stage 4 cirrhosis?. Did I

read that right? It was a Roche study using Shering drugs?

Stranger things can happen I guess. Happy for you.....your friend...ric

Link to comment
Share on other sites

>

> Thats great news Pete. were you into stage 4 cirrhosis?. Did I

> read that right? It was a Roche study using Shering drugs?

> Stranger things can happen I guess. Happy for you.....your friend...ric

I'm stage 1 inflmation only. The fatigue has been bad enough at this

level - I can sympathize with those with worse damage than me.

It was a Schering Study and I was in the control group using Roche

drugs. I had a very standard dosage: 1 ml of interferon and 1200 mg of

ribavarin daily. That ribavarin is what is giving me sides - getting a

persistent cough from it.

Pete

Link to comment
Share on other sites

>

> Thats great news Pete. were you into stage 4 cirrhosis?. Did I

> read that right? It was a Roche study using Shering drugs?

> Stranger things can happen I guess. Happy for you.....your friend...ric

I'm stage 1 inflmation only. The fatigue has been bad enough at this

level - I can sympathize with those with worse damage than me.

It was a Schering Study and I was in the control group using Roche

drugs. I had a very standard dosage: 1 ml of interferon and 1200 mg of

ribavarin daily. That ribavarin is what is giving me sides - getting a

persistent cough from it.

Pete

Link to comment
Share on other sites

> We all have our bd moments Pete......but right now it's time to

>

> CELEBRATE!

>

> To bad I can't put graphics......but imagine balloons and a sign

with bright

> colored letters that says.....

>

> CONGRATULATIONS!!!!

>

> Love,

> Nursey

Thanks so much for the good vibes. The struggle is so much easier when

we have companions of like mind. I feel like reaching to hug everybody

here.

Togeather

Each

Achieves

More

Pete

Link to comment
Share on other sites

> We all have our bd moments Pete......but right now it's time to

>

> CELEBRATE!

>

> To bad I can't put graphics......but imagine balloons and a sign

with bright

> colored letters that says.....

>

> CONGRATULATIONS!!!!

>

> Love,

> Nursey

Thanks so much for the good vibes. The struggle is so much easier when

we have companions of like mind. I feel like reaching to hug everybody

here.

Togeather

Each

Achieves

More

Pete

Link to comment
Share on other sites

annita

please let us all know what you find out about your thyroid,, if you dont like

this doc, then go to another one,, dont give up!

ms seven wonders wrote:

Hugs to ya

okseven_7

__________________________________________________

Link to comment
Share on other sites

annita

please let us all know what you find out about your thyroid,, if you dont like

this doc, then go to another one,, dont give up!

ms seven wonders wrote:

Hugs to ya

okseven_7

__________________________________________________

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...