Thursday, May 31, 2012

Caden's Surgery today!

Hi everyone,

Please please please pray hard today for our little friend Caden and for his family David, Melissa and Griffin.  Caden has HLHS and he is having his 3rd surgery today to repair his heart.  I know this is a big surgery and Caden is going in very, very strong.  He has been such an amazing fighter for these past 3 years.  Just one more.......I know he can do it!  You can check out his blog here...

http://www.thesmithsbaby.blogspot.com

Caden, we are praying for you buddy!  Hang in there and fight away.  Love to you and your family,  Susie

Wednesday, September 14, 2011

Fall school pictures



Brynlyn's 2011 Fall Kindergarten pictures-age 5

She just looks so grown up to me. Wow, five years old!? When and how did that happen? =)

I am a total hook-line-sink when it comes to school pictures. The picture company can see me coming from a mile away! ha ha

I loved when I was younger and had my pictures taken and my Mom always bought the full package deal so I still have prints of every year of me in school and now I love it when it's picture day for my girls! This year I opted to order the CD instead of prints so I can reprint whatever pictures I want to reprint and not to buy their package deal. Don't get me wrong, it still cost a small fortune, but it's always so worth it in my mind! I always think that they'll only be this age once and so I need to make sure it's captured on film and school pictures are so classic and iconic. I'm sure (and hope) my girls will appreciate it as they grow up. =)

Enjoy your child's picture day!!!

Tuesday, August 02, 2011

Angel Paige

Hi friends,

Yesterday I attended the funeral memorial service for a dear friend's little 18 month old heart baby daughter Paige who unexpectedly passed away due to complications with her heart defect.

This is the link to her blog where you can learn more about sweet Paige and her courageous family...

www.jamie-bloomfieldfamily.blogspot.com

It was an amazingly beautiful and heartfelt service yet we are all so sad at the loss of sweet Paige and our hearts go out to Jamie, Keith and their entire family as they begin to heal from this loss.

Paige is such a darling girl who was so full of life and she truly was such a light in this family. Please pray for this sweet family as they struggle to put the pieces back together following the loss of sweet Paige. We will remember her forever and she will always be in our hearts and we are so thankful for her strong example of happiness and courage despite all of the health struggles she fought for the last 18 months.

To the Bloomfield family, we love you guys so much and we will continue to pray for you that Heavenly Father may continue to carry you in His loving arms as your hearts begin to heal from your loss.

Sunday, August 23, 2009

Angel Ethan

A sweet and courageous little guy Ethan has returned home to his Heavenly Father. We just met this family last night and they had just lost their sweet one the night before. They are truly an amazing family and such an inspiration to us. I'm sure they can use all of our prayers during this difficult time.

You can read about courageous Ethan and his incredible family at www.crazyskids.blogspot.com

Sunday, May 31, 2009

What a difference two years makes...

This blog post is DEDICATED to Caden, Melissa and David Smith and their families, the Smiths and the Monroes.

Caden and Brynlyn share something very special and unique in common: They share the same date (May 29th) as their second heart surgery date.

May 29th, 2009: Caden's 2nd heart surgery

May 29th, 2007: Brynlyn's 2nd heart surgery

We checked Brynlyn into St. Joseph's Hospital so she could undergo her 2nd open heart surgery. This was full reconstruction and a doozy of a surgery. She came through it with just some minor bumps along the way, but she was a trooper and fought it all the way home. We brought her home 7 days later and we haven't looked back since. Now, Brynlyn is an almost 3-yr-old darling, spunky, and full of life baby girl. She has this dark brown hair that has tight curls all over her head that look like Annie. She's as smart as a whip and spunky as all get out. She can be a girl with a 'tude whenever she wants to be, but most of all, she's cuddly, cute, and sweet as can be. We cannot possibly imagine our life without our little DiGeorge baby and I can honestly say that we are so GRATEFUL for all of the challenges that come with Brynlyn, including tough days, great days, sick days, healthy days, happy days, sad days, upbeat days, bummer days...but mostly ANY DAYS that Heavenly Father lets us have with our sweet fourth daughter! Brynlyn has taught us the sacred nature and precious nature of life and how we truly must enjoy each day, each moment that we have with one another. And for these lessons and more, we are truly grateful.

So to the Smiths and the Monroes, you will look back on this very pivotal day in Caden's life and remember all of the things (good and bad) that you have learned from this experience and you will be grateful for them all, for these experiences are shaping you into the person that God wants you to be.

In a few years from now, Caden will be jumping and hopping around as a happy toddler and you will be so grateful for everytime you have to pull him down from climbing on the table and furniture, and you'll remember a day a few years before, when he was having his heart worked on...........


Brynlyn in recovery, fresh from surgery. And to answer your question, NO, you never, ever get used to seeing your child like this.

All of her medications, tubes, monitors, keeping her in check. Thank heavens for modern technology. I'm afraid to say that Brynlyn would never have survived crossing the plains with the pioneers.

Me and Brynlyn in pre-op just moments before surgery. I was wearing my little Gap T-shirt with a heart on it that said "Sweet Heart" and this darling necklace that my dear friend (and heart mommy April Layton) gave to me that is in the shape of a heart and says CHD (congenital heart defect). The look on my face says, "And you think you're taking my daughter WHERE to do WHAT? I don't think so!!!!!" ha ha
Just a few minutes after this, after they took Brynlyn to pre-surgery prep, I spent the next 20 minutes in the bathroom crying my eyes out. Yep, just another day, just another heart surgery.......

Brynlyn with Daddy right before surgery. She was a chunky monkey, and technically in congestive heart failure. Yep, she needed this surgery. Thank heavens for a wonderful team of doctors and nurses and hospital and staff that took such great care of us. But quite honestly, I don't care to see them for a while. I think I'll keep my baby at home with me and enjoy her for a little longer before I have to take her back to them. =)

So Caden and Family, Hang in there! Fight the tough fight, and never give up. You have people all over the world praying for you and for Caden's recovery. Try to stay optimistic at all times and always know that God is holding Caden's hand through this. Faith and Hope (and lots of chocolate) will get you through many, many tough days.
We love your family and we are always thinking of you. Please let us know if there's ever anything we can do!
love,
The Jensen Family



Caden Smith

Hi there,

Our dear little friend Caden Smith just underwent his 2nd surgery to repair his Hypoplastic Left Heart Syndrome. He and his parents had a rough day (and for you heart mommies and daddies out there, you know exactly what that means.)

They could use all of our faith and prayers to help them through this difficult recovery process. I know they would appreciate it.

You can read more about sweet little Caden at:

www.thesmithsbaby.blogspot.com

We wish you all happiness and good health!

Sunday, January 25, 2009

Heart Poem


Heart Poem...

anonymous author


It's a beautiful day up in heaven. Jesus is rounding up his tiniest angels, to go live on earth, and be born. One of the sweetest angels says to Jesus "I don't want to leave, I like it here, and I will miss you". He reassures the scared little angel that everything will be okay, and that she is just going for a visit. She is still not swayed on this idea.


So Jesus kneels down, and says, "How about if you leave half of your heart here with me and take the other half with you, will that be okay?" The angel smiles and says, "I guess that will work". But the little angel is still a little scared.


She asks,"Will I be okay with only half of my heart?" Jesus replies,"Of course you will, I have other angels there that will help out, and you will be fine." Then Jesus gives the angel more details about his plan. He says "When you are born, your mommy and daddy will be scared, so you have to be strong, and when you feel weak just remember that I have the other half of your heart".


"Enjoy your time with your family, play and laugh everyday." "And when its time to come back to heaven, whenever that may be, I will make your heart whole again. Always remember that you are not broken, just torn between two loves."


Wednesday, January 07, 2009

Jersey Anderson

Little sweet baby Jersey Anderson earned her angel wings on Monday, January 5th, 2009, as she left this world and now lives in heaven with our Heavenly Father. Our thoughts and prayers go to her oh-so-sweet family, the Anderson family, as we all mourn the loss of their sweet baby.

You can read about Jersey girl on their wonderful blog at http://www.andersonsavenue.blogspot.com

We send much love to the Andersons at this difficult time. Jersey has had such an amazing impact on so many lives and her ripple effect of love will be felt throughout my life and so many other lives forever. Thank you for sharing your baby's courageous journey and tough fight with us. Your entire family's strength, courage, hope, love and faith has been a testimony to me and to my family. We will continue to pray for you all for peace and comfort and love and for Heavenly Father to hold you in the palm of His loving hands during this very difficult time.

Love,
The Jensen Family
heart
Photobucket
chd, children, heart, defect
CHD Awareness site
22q 22q11 22q11.2 vcfs digeorge syndrome