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Excellent! Way to go OneStepAhead for recognizing

plagio in their advertisement!!!

& JD (DOCband since 2/26)

TX

-----Original

Message-----

From: sponagle2003

<sponagle2003@...> [mailto:sponagle2003@...]

Sent: Thursday, February 27, 2003

7:15 PM

Plagiocephaly

Subject: Re: Sorry

> > I tried to put a website for a plagio-preventer type thing. It

> > obviously did not work....I am sorry...I am going to hide

> > somewhere....

> >

> > Sponagle

For more plagio info

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We bought one of those and Kirsten refused to sleep on the pillow

part, she would roll off of it and continue to lay on her left side.

It seemed like it would help, but if you have a stubborn baby . . .

Mom to Kirsten & Jocelyn banded 2/21/03

> > > > I tried to put a website for a plagio-preventer type thing.

It

> > > > obviously did not work....I am sorry...I am going to hide

> > > > somewhere....

> > > >

> > > > Sponagle

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  • 11 months later...

I’m sorry if I, among others, misunderstood your optimism. I too

started out with the attitude that I’d be different, not need all those

meds. I’ve been forced to compromise in order to live my life to the

fullest extent possible. We all have the same desire, deep down: to

continue with the life we envisioned for ourselves. You’ve been fortunate

to be able to do that with a minimum of difficulty. Hopefully you’ll be

able to continue on the same path indefinitely.

One could say I take too much medication, but my story can be seen as

optimistic as well. I’ve found a way to compromise, come to terms with my

limitations, and although I’m not living the life I envisioned – I have

forged a new direction. I’ve built a business where, rather than fight my

disability, I can work with and around it. When I’m working full time at

it, I actually make as much as I would with my degree. Is it the life I

spent my youth planning and dreaming of? No. But I haven’t given up,

either.

Keep fighting, ! It’s all any of us can do when faced with this. And

we all learn from each other here.

Hugs,

Carol

[ ] sorry

My apologies to all that I seem to have offended. I have a mother

who has had severe RA for many years and I do know the devastating

affects of this progressive disease. I am scared to death about

what my future holds. When i was diagnosed , my Rheumatoid factor

was 10 times the normal range, the highest my doctor has ever seen

and so that does not bode well for my future, since those with such

high titres often have the most severe disease. But for now, i'm

doing reasonably well and I was just trying to present a positive

story.

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, I think we'll all be fine about this - and I mean you, too. I'm

sure you didn't mean to hurt Carol or anyone else here with your

comments.

We had a lively discussion, and I hope everyone has come away learning

something new about themselves, others, or RA.

As many of us know, some doctors do indeed do what you alluded to -

prescribe drugs without thinking things through, prescribe too many

drugs, or, under pressure from the patient, give the patient something

that will satisfy that may not be in the patient's best interest.

That's why we're here. To learn about such situations and protect

ourselves and each other.

So, let's all move forward now and focus on supporting each other in the

most positive ways we can!

I'll tell you where to go!

Mayo Clinic in Rochester

http://www.mayoclinic.org/rochester

s Hopkins Medicine

http://www.hopkinsmedicine.org

[ ] sorry

> My apologies to all that I seem to have offended. I have a mother

> who has had severe RA for many years and I do know the devastating

> affects of this progressive disease. I am scared to death about

> what my future holds. When i was diagnosed , my Rheumatoid factor

> was 10 times the normal range, the highest my doctor has ever seen

> and so that does not bode well for my future, since those with such

> high titres often have the most severe disease. But for now, i'm

> doing reasonably well and I was just trying to present a positive

> story.

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  • 2 months later...
  • 3 years later...

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