Cystic Gal

The daily ponderings of Beth Peters as she writes about Cystic Fibrosis and lung trasnplant.

Friday, November 20, 2009

Vid with Me and S-Artee

Watch
this
video by clicking HERE!

- November 20, 2009

Email This BlogThis!Share to X Share to Facebook Share to Pinterest

Labels: videos

1 comment:

Lucy11/24/09, 3:01 PM
Excellent to see you here and see your sister win the Transplant Olympics - wow. Thanks for hangin with me today - super-wonderful to see you in person and meet your mommy.

xxoo
ReplyDelete
Replies

Add comment

Thanks for commenting! Your comment will be posted ! (probably)

Newer Post Older Post Home

Subscribe to: Post Comments (Atom)

New Blog and Site

Yo Old Friends! It's me, Beth Peters / CysticGal / the artist actually known as Mary ElizaBeth Peters . I am moving on from this bl...

Ten Things A CG Wants To Say: The post so crazy even my disclaimers need disclaimers.

1. To the guy that broke up with me right after I got out of the hospital: You are cowardly, and selfish, and also bald*. 2. To the neighbor...
Guest Blog by CysticLady: Update on CysticGal II

Tonight I got calls from CysticDad and CysticMommy saying that they are moving CysticGal to the ICU. She's just not breathing very well...
Home Again, Home Again, Jiggetty Jig

This'll be yet another quick post to hopefully launch me into posting more often. I finally arrived home on Thursday late afternoon, and...

Search This Blog

WOAH 100,000 Unique Readers! And Counting!

View Stats at StatCounter ; View Stat Summary by CG

Blog Archive

► 2020 (1)
- ► June (1)

► 2019 (2)
- ► June (2)

► 2013 (3)
- ► April (3)

► 2012 (18)
- ► December (1)
- ► June (1)
- ► May (8)
- ► April (6)
- ► February (2)

► 2011 (17)
- ► December (2)
- ► November (1)
- ► October (3)
- ► May (2)
- ► April (2)
- ► March (2)
- ► February (2)
- ► January (3)

► 2010 (255)
- ► November (15)
- ► October (7)
- ► September (17)
- ► August (30)
- ► July (34)
- ► June (42)
- ► May (35)
- ► April (21)
- ► March (20)
- ► February (16)
- ► January (18)

▼ 2009 (171)
- ► December (15)
- ▼ November (16)
- ► October (22)
- ► September (32)
- ► August (27)
- ► July (37)
- ► June (22)

Labels

after transplant
anger
anxiety
apppintments
articles
asthma
bipap
bloggers
blogiquette
blood pressure
boobs
CF Adult issues
CF organizations
CG Developments
children with CF
cleveland
clinic
coughing
Current Health Update
Cystic Fibrosis Foundation
Cystic Lady
Cystic Mommy
disclaimers
dreams
ears
employment issues
exercise
family
fashion
food
friends
fun on a sick day
genes
germs
holidays
hospital
ICU
independence
inspiration
IVs
just the news
letters
Mask Up to Meet Up
meds
merch
mood
music
non-cf
nurses
Old Navy
oxygen
pets
PICC lines
pictures
poems
poetry contest
Ports
Pulmonary Endometriosis
putting the "Gal" in "Cystic Gal"
Q/A
rant
real housewives
resources
romance
sites
sleep
spiritual stuff
statcounter
support
t-shirts
television
The Call
The Future
The Past
The Recent Past
The Vow of the Cardio
tips
top ten lists
transplant
travel
u
UnBlog
Unleash Your Story
Unto the East
Valium
videos
vulnerability
ways to give back.
work
yoga
yuckies

Email Me! I love to receive questions and topic ideas!

BethPetersBoston@gmail.com

AdSense Search

New to CG? Read this first!

Click on this picture to learn about the moderator of the blog and its original purpose

Blogs We Love to Love

The Unknown Cystic » Fox’s Communications Tips: Speaking to RTs

Still alive and kicking - It’s been a long time since I posted. I’m not sure why. Here’s what I’ve been doing. Competing in scentwork trials with my golden retriever (he’s awesome) ...
My Thoughts

Friendships - I've never been one to have a plethora of friends. In high school there were four of us that hung out all the time. I honestly cannot remember what happene...
donorcycle

The last will be first, say what now? - What does it mean, the last will be first? My pastor, Seth Kaper-Dale, is running for governor of NJ**. His campaign slogan is, “The last will be first.” ...
I have CF. So what?!

Why Trolls will make you re-evaluate your life - If you haven't seen Trolls yet, save it for a day when you need to be reminded that we do, in fact, choose to be happy or we choose to be miserable. We al...
nevering

farewell nevering - This blog was started several years ago as a small way into my world of writing. It has been a notebook for oddments, a place to share early drafts, com...
Run Sickboy Run

My New Treatment: O to the 2 - I recently started a new treatment that was probably long overdue and needed for quite some time. At the request of our brand new adult CF doctor, I did a ...
Not so bright and shiny

This moment... - Well...I can't say that I'm surprised. It's been so long. I felt a tug to write. A need to gather my thoughts in one place and free them from spinning in m...
Every Life has a Story to Tell

A little redneck ingenuity saved the day... - So on a fairly regular basis, I travel for soccer. I coach some high-school aged girls on a club travel team and we travel the state, and a few neighborin...
My journey with Cystic Fibrosis

Rest in Peace Aunt Marybeth - Monday my Aunt passed away. She had pancreatic and liver cancer. The past two months she has been hospitalized and this was expected, but not expected. ...
Breathing For A Living

We did it! It's official!! - Three days after Christmas and one day before my 33rd Birthday I have some wonderful news to share! My coordinator at Cedars-Sinai called me this afternoon...
Welcome to Joshland

It's All Good In Joshland -
Phoenix's Fight

Resep Kue Tart Spesial Enak - Langkah Bikin Kue Tart Empuk serta Istimewa – Hidangan kue tart memanglah telah jadi hal yang umum untuk di hidangkan di perayaan lagi th.. Kue tersebut te...
sick girl speaks!

I'm back. - I'm back. More to come!
I have CF, but it will never have me!

Bad news - You know when people tell you do you want the good news or the bad news? We all know that the bad news must really suck. I've learned my lifetime when it c...
A Matter of Life and Breath

What I Know Now - Here we go again. In so many ways it feels as though the last year or so has been a total whirlwind. We've now gone through a full set of seasons since I o...
Tina's river

Niagra, The TA, and meltdowns - This was written in 2009...found in drafts. (Clearly I have not yet mastered putting F'ing photos on my blog) Anyhoo we made the trip to Buffalo to see o...
CF Steph

Where has time gone? - I cannot believe it has been over 4 years since I have created a new post on my blog. My plan was to keep the blog going after my double lung transplant bu...
Jess's Journey

Valuable tips on how to learn Arabic the right way - You might have come across with numerous people who have an interest in learning diverse languages. Some do it as a hobby where as there are few who have t...
Confessions of a Cyster

Minding My Own Business - So, I was just trudging along... I had been minding my own business, doing exactly what was expected of me. I had a tough summer after needing to have ab...
Confessions Of A CF Husband

Six Years - I'm reminded of it every day, knowing how radically different the past six years could have been without the gift of Tricia's first donor. Should your fam...
My Journey

Ultimate Savory Pot Roast w/Gravy - Back in February Me, my sister Jessica, my mom Heather, my cousin Kasey and a good friend of ours Barb went to see *The Addams Family* play here at our lo...
My CF Journey With God

Graduation and Health Update - I'm sure most of you thought I had abandoned my blog....I apologize. Unfortunately you are still stuck with me as I hope to be updating more often now that...
Breath Sentence

Great Strides 2012, Or: Why You Should Give Me All Your Money - Great Strides is the biggest annual fundraiser held by the Cystic Fibrosis Foundation, with 5k walks smattered all across the country, mostly in the spring...
“If you smile when no one else is around, you really mean it.”

Brandi, 1978-2012 - For those of you who have been following Brandi's blog, we want to let you know that she lost her battle with Cystic Fibrosis on Wednesday, February 15, 20...
Justine

I'm Still Here! - If you're looking for updates, go to my CaringBridge page. I'll continue updating that until I get to leave Minnesota! http://www.caringbridge.org/visit/n...
The Other Side

Feeling lost - I feel so lost without Gessner. I'm not sure that I ever thought that I would say that. I fancied myself an independent woman. But the truth is that Gess w...
Journey of a Lifetime

2011 - Time for a little update. Life has been really good. For the first time in many many years I am really enjoying winter time. I love the snow, the chill, al...
A Day In The Life of a CF Mom

Needle? What needle? - No sooner did we finish giving thanks did Lucy have a clinic day. There were a few things that I really needed to discuss yesterday with her whole team of ...
Another Outlet

No Rejection Bronch 3.... - Yes that's right, got the results back earlier today and there is no signs of rejection in the tissue pathology. They decided that they will not treat the ...
I am Samuel's Mommy

We've moved - Well, I've moved. I'll be blogging over at cfmommee.blogspot.com Come over and check it out!
Breathing Deeply: My Life With Cystic Fibrosis

Remembering Lauren - If anybody's still checking this page, I wanted to point you to a post I wrote on my own blog about an award that was presented recently in Lauren's memory...
Teeda Blog

Nondate-out... Unboyfriend... Breakup? - I was once married to a man that I'm quite sure to this day would take a bullet for me. Sometimes things in your life break your relationships. For me, t...
Endurance For a CF Cure

-
Letsdothis

-

Show 5 Show All

Are you a cystic gal who loves to write?

Visit Patient Press and Submit Your Work!

Public Followers

Goals of "Cystic Gal" for READERS AND CONTRIBUTORS!

I Want This Blog To Be:
1) A place to get feedback
2) A place to e-meet people
3) A place to express our shared story
4) A tool for dealing with our fears and anxieties
5) Funny and Balanced.

I Don't Want This Blog To Be:
1) A personal diary
2) A rant page
3) An oversimplification of CF, either positive or negative
4) A place where we judge other CFers' coping mechanisms or circumstances.

What's-A-Mattah-You?

Click HERE to Read My Crazy A** CG Disclaimers!

. . .

Home

Contributors

Beth Peters
Cystic Gal
Patient Press
Teeda

This page is creative writing, and not to be taken as medical or actual fact, ever, for serious. Watermark theme. Powered by Blogger.