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Robertson

HealingWell Forum
>
Member Profile
Display Name
Robertson
Profile Created
11/17/2005 8:10 PM
Last Seen
4/29/2006 2:14 PM
Total Posts
21

Last 50 Posts

I Have A Few Questions????

I would ask the doctor about phenagren for upset stomach...

4/21/2006 11:01 AM

Cystic Fibrosis
cf

Hi Frank, Welcome Congrats. on staying so healthy. As for your lack of smell, I'm not sure why but I have the same thing. although I can smell if it's a strong smell. Oh by the way, my name is Mark...

4/18/2006 9:42 AM

Cystic Fibrosis
New to the boards

Hi Chaser Welcome, glad to hear your doing well these days. keep up the good work. :tongue:...

4/18/2006 9:31 AM

Cystic Fibrosis
SMILE!

Wow Sarah, You got enough on your plate. You have an awsome attitude. keep it up. :smurf:...

4/14/2006 9:47 PM

Cystic Fibrosis
looking for fellow cf'rs

So Neely How is the CF centers, and insurance there in Australia. Do you find that the doctors know allot about CF :scool:...

4/14/2006 9:29 PM

Cystic Fibrosis
Sound Off: CF Member Room

hi twinstridede No my voice is fine. as for the rest of me, working good although my sugars have been bouncing around lately...

4/13/2006 2:25 PM

Cystic Fibrosis
looking for fellow cf'rs

/community/emoticons/smile.gif Hi Neely Mark here 42 w/CF Welcome. Theres alot of great people here to get to know. you shouldn't have any trouble making friends...

4/11/2006 9:48 PM

Cystic Fibrosis
The TidBit Info Room!

/community/emoticons/yeah.gif Eat often, not always full meals but often, and do those treatments...

4/11/2006 9:44 PM

Cystic Fibrosis
I am playing a character who has CF....please help

You know Autumn06 I seem to remember you asking for input about a paper you were doing a while back. Now your doing a play, c'mon what do you realy want....

4/11/2006 9:29 PM

Cystic Fibrosis
Hello world!!!!

/community/emoticons/nono.gif I 42 w/CF and I've got to tell you that there realy is no alternative. I've been battling this to long and searched for that "alternative" for ever. When my PFTs sunk...

4/11/2006 9:18 PM

Cystic Fibrosis
gf in general

/community/emoticons/tongue.gif Hi jdgal My name is Mark, Im 42 w/CF I had a bi-laterl transplant in 2003. If you have any questions feel free to ask. robertsonms@comcast.com ...

4/11/2006 9:10 PM

Cystic Fibrosis
lobectomy vs lung transplant?

I was offered a lobectomy or transplant. I chose the transplant only for the reason that my pft's were to low as it was. Taking a part of my lung would have made it worse. but since my Transplant I...

4/8/2006 12:05 PM

Cystic Fibrosis
Should I be scared?

/community/emoticons/confused.gif May you need to have a talk with your Doctor. and see if it's time to be put on a Transplant list. It gave me a new life. If the dr. doesn't think your ready, ask...

4/8/2006 11:56 AM

Cystic Fibrosis
Living with CF,turning 18..and can't help thinking...am I at midlife?

Yes, it's true I have a healthy 16 yr. old son. and yes all by myself. besides my wife he is the greatest thing to happen to me....

4/8/2006 11:43 AM

Cystic Fibrosis
Sound Off: CF Member Room

hey Twinstride, answer to you question. My lungs are perfect. My PFTs are in the high 90% I feel awsome. /community/emoticons/yeah.gif ...

4/8/2006 11:36 AM

Cystic Fibrosis
Living with CF,turning 18..and can't help thinking...am I at midlife?

Hi Missy Let me tell you something. You can have a long life ahead of you. In Sept. I will turn 43 all you have to do is take care of yourself and do everything those doctors tell you. Make sure you...

3/31/2006 12:26 PM

Cystic Fibrosis
Sound Off: CF Member Room

My name is Mark Robertson, I'm 42 and have CF. I live in Oregon /community/emoticons/yeah.gif I'm two and a half years past my double lung transplant, and doing awsome....

3/31/2006 12:14 PM

Cystic Fibrosis
My Introduction

Way to go! Wives have that knack for keeping their husbands in line. It's that love thing and wanting to keep you around. My wifes been doing that for almost 16 years now, along with my son....

1/20/2006 3:04 PM

Cystic Fibrosis
Genetic Mutation? (Post it here)

I've lived with CF all my life, I'm now 42. I recently found out that there was different stains. I dont know what mine is. I am now 2 1/2 years post transplant, and doing great...

1/20/2006 2:54 PM

Cystic Fibrosis
SMOKING WITH CF

I know someone who did start smoking. Take my advice, DONT it made things alot worse...

1/20/2006 2:46 PM

Cystic Fibrosis
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