caelengorman.blogspot.com

Caelen Gorman

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 27, 2015. I know I haven't updated since FL GA Line concert, but those of you on FB have watched Caelen's updates, so I'm only partly behind. Speaking of, if you haven't already seen, I created a FB page just for Caelen it's called Super Caelen, check it out:. Https:/ www.facebook.com/SuperCaelen. There are even more excitin...

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Caelen Gorman | caelengorman.blogspot.com Reviews

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My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 27, 2015. I know I haven't updated since FL GA Line concert, but those of you on FB have watched Caelen's updates, so I'm only partly behind. Speaking of, if you haven't already seen, I created a FB page just for Caelen it's called Super Caelen, check it out:. Https:/ www.facebook.com/SuperCaelen. There are even more excitin...

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Caelen Gorman | caelengorman.blogspot.com Reviews

https://caelengorman.blogspot.com

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 27, 2015. I know I haven't updated since FL GA Line concert, but those of you on FB have watched Caelen's updates, so I'm only partly behind. Speaking of, if you haven't already seen, I created a FB page just for Caelen it's called Super Caelen, check it out:. Https:/ www.facebook.com/SuperCaelen. There are even more excitin...

INTERNAL PAGES

caelengorman.blogspot.com

1

Caelen Gorman: October 2014

http://www.caelengorman.blogspot.com/2014_10_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Sunday, October 19, 2014. But come on, has anyone ever seen Caelen get stage fright? But overall, it was an absolutely amazing experience, and I can't thank Brian, Tyler and their team enough for giving us that gift. Plus.they totally rocked it! How lucky is Caelen that his first concert was FGL? Mine was Paul Anka, thanks mom. Captain Ma...

2

Caelen Gorman: December 2013

http://www.caelengorman.blogspot.com/2013_12_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Tuesday, December 24, 2013. Merry Christmas Eve to all of our friends. We just had a wonderful family dinner with our friends the Cohens again, and it was more reflective this time for me. Merry Christmas to all, and to all of our prayer angels, we wish you a good night. And a Happy Anniversary in Heaven to Grandma Doris and Grandpa Joe.

3

Caelen Gorman: August 2014

http://www.caelengorman.blogspot.com/2014_08_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, August 22, 2014. Celebrating 5 with a cover story. There is so much good going on right now that I have to try and contain my excitement in this blog. I will try and minimize additional exclamation points, but it's going to be hard.cause I'm so excited! First off, Caelen is doing really well! Now, on the the good stuff! Twice as m...

4

Caelen Gorman: March 2014

http://www.caelengorman.blogspot.com/2014_03_01_archive.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 28, 2014. This one's for you Weston. I returned last night from Weston's memorial and celebration of life in Philly. It's hard to sum up all of the 24 hrs of my short trip, but if there is one word I could use, it would be Love. All of our lives will go on, and we should make the most that we can with the time we're given.

5

Caelen Gorman: Timing

http://www.caelengorman.blogspot.com/2015/03/timing.html

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 27, 2015. I know I haven't updated since FL GA Line concert, but those of you on FB have watched Caelen's updates, so I'm only partly behind. Speaking of, if you haven't already seen, I created a FB page just for Caelen it's called Super Caelen, check it out:. Https:/ www.facebook.com/SuperCaelen. There are even more excitin...

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macsenthegrayt.blogspot.com

Events | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/p/events.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. March 21 at the Grace Place Church in Enterprise, Al we will be having a spaghetti dinner. All $ raised will go towards Macsen's medical care, travel and lodging expenses. Boland Lanes in Enterprise on July 28th, 2012. Asking $10 donations for each person to bowl. Includes 3 games and shoes. Please RSVP before July 21st, so we can get an accurate number of attendees so they can reserve our lanes! Subscribe to: Posts (Atom).

macsenthegrayt.blogspot.com

October 2014 | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/2014_10_01_archive.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Friday, October 24, 2014. This post is from October 7 but failed to upload*. Today was a good day. I picked up donations from 2 Moms Club mommies - stuff for the big yard sale this Saturday. Macsen even got an impromptu play date out of it - he had a ton of fun playing with a one of their little girls. He's so smart - he just kept giving her toys, keeping her happy, smart man. He played really well all day - rubbing his face in ...

macsenthegrayt.blogspot.com

March 2015 | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/2015_03_01_archive.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Feed the Fire for Weston. Monday, March 23, 2015. Spaghetti Dinner was a success! Sunday, March 22, 2015. Despite all my doubts and worry we had a great turn out for the dinner and more than enough help and supplies to pull it off. Saturday, March 14, 2015. Crazy I would be so excited about that but it felt good to clean and he wasn't crying, holding onto my leg which I cannot stand for very long. He's just too pitiful. They wer...

macsenthegrayt.blogspot.com

April 2015 | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/2015_04_01_archive.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Wednesday, April 29, 2015. Macsen Graybeard the Pirate. We finally have a tentative cath date! Racing Kis to the kindergarten. Monday, April 27, 2015. Saturday, April 25, 2015. We had a great time at the heart walk in Atlanta this weekend. We helped raise $76000 for the Childrens Heart foundation! Subscribe to: Posts (Atom). Other ♥ Families. New Care Package Items. Facebook fundraising page - Ask to join! Promote Your Page Too.

macsenthegrayt.blogspot.com

August 2015 | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/2015_08_01_archive.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Monday, August 31, 2015. Macsen's appointment went well today - chest X-ray was "beautiful," his breathing looks good, he's drinking milk again, his chest tube suture was removed and his O2 saturation was 90! We get to lower his dose of his 2 diuretics and when we asked when we need to come up next his cardiologist said the most beautiful words "not for 3 more years (if he continues to do well)! Discharged from the hospital!

macsenthegrayt.blogspot.com

Help? | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/p/want-to-help_16.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. He will never be "fixed." He will always have half a heart and will always need monitoring, echos, EKGs, tests, tests,tests. We hope after this 3rd surgery we can take this "Help" page down because we will be living more like a normal family. 100 % of donations made through Paypal from another Paypal account go to our family for Macsen's care. All other donations made to Paypal through credit cards have a fee removed by Paypal.

macsenthegrayt.blogspot.com

BabyPics | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/p/babypics.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Macsen @ 8 weeks looking like a gummy bear. 20 weeks looking right 2 the ultrasound thing - the girls never did that! 22 weeks and looking like his Daddy. 36 weeks 5 lbs 12 0z. Subscribe to: Posts (Atom). Macsen eating never gets old. Other ♥ Families. New Care Package Items. Facebook fundraising page - Ask to join! Promote Your Page Too. Aaron J. Miller. Blog contents © The Adventures of Macsen the Grayt.

macsenthegrayt.blogspot.com

Our Story | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/p/our-story.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. I wrote this soon after we found out about Macsen's heart at 20 weeks pregnant. He said the baby has Hypoplastic Left Heart Syndrome - or small left heart. That our little man will need lots of surgeries. I've created this blog to help keep family informed, to help people praying for us and the baby have a name and a face to pray for, and to help keep me sane. August 14, 2012 at 9:45 AM. Subscribe to: Posts (Atom).

macsenthegrayt.blogspot.com

November 2014 | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/2014_11_01_archive.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Tuesday, November 25, 2014. Tonight and for the next few days we hope to get lots of rest. None of us have slept well in 5 days and with the stress of everything we are just exhausted. Looking forward to the king size bed at my sister's house and seeing our girls. So great news so far. He is still getting his cath. Will update when we know something. Update at 11. Cath is going well. Another update at 12. Now we are waiting on a...

macsenthegrayt.blogspot.com

Nana has arrived | The Adventures of Macsen the Grayt

http://macsenthegrayt.blogspot.com/2015/08/nana-has-arrived.html

The Adventures of Macsen the Grayt. A Chronicle of Our Experience with HLHS. Friday, August 14, 2015. Subscribe to: Post Comments (Atom). We started it in May 2012 following our unborn son's HLHS diagnoses. He is currently 2 and waiting for his 3rd open heart surgery. This blog gives us a place to reach out to other families, to have an outlet to vent and share, and to document our journey with our baby we call Macsen the Grayt. Discharged from the hospital! Not getting out of here today. Day 5 post op.

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SuperCaelen

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caelenbird.net

C. Bird Art Portfolio

Thanks for checking out my art on the web! Show your support and keep up with news and new paintings on Facebook: Caelen Bird, Artist and Musician fan page. SOLD 50 x 32 Pointalism-like. SOLD 50 x 32" Pointalism-like. 50 x 32" Large painting by C. Bird SOLD. More info and pricing. SOLD Green apple on gray. SOLD Oil on canvas. 24" x 24". More info and pricing. Oil on canvas. 10" x 10" $95. More info and pricing. Oil on canvas. 13" x 16" $225. More info and pricing. Oil on canvas. 29" x 29" $400.

caelencolquhoun.org

Caelen - Home

WBC: Way Before Caelen. Clan Colquhoun: A Fathomable History. Clan Johnstone in Scotland. CaelenColquhoun.org was created to help Caelen, a new addition to Clan Colquhoun on January 11, 2014, grow up with an awareness of his ancestry. Caelen's Dad is Clan Colquhoun and Caelen's Mom is Clan Johnstone: Through this website we want to give Caelen an opportunity to learn the histories of both clans, and give clan and family members the opportunity to know of Caelen. Clan Colquhoun Crest and Tartan.

caelencotter.com

Monster web site – about giant monsters that fight and alins and predtors that fight

About giant monsters that fight and alins and predtors that fight. It seems we can’t find what you’re looking for. Perhaps searching can help. Proudly powered by WordPress. Theme design by Elevate.

caelene.com

Considered Opinions

This blog reveals my passions, pursuits and opinions! Thursday, January 5, 2017. Have you ever really pondered the scene between Mary and her son in John 2:1-10. This is such an interesting passage of scripture. Not only Mary’s request of Jesus, but Jesus’ response to his Mother. Even though the “timing” may not have been perfect, what was perfect was the obedience to Jesus, and the honour that was bestowed by Jesus to his mother. What encouragement for us. He can turn water into wine. This revea...Maybe...

caelengenharia.com

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caelengorman.blogspot.com

Caelen Gorman

My day to day life with an amazing little boy named Caelen who was born on August 17, 2009 with a congenital heart defect called HLHS - Hypoplastic Left Heart Syndrome. Friday, March 27, 2015. I know I haven't updated since FL GA Line concert, but those of you on FB have watched Caelen's updates, so I'm only partly behind. Speaking of, if you haven't already seen, I created a FB page just for Caelen it's called Super Caelen, check it out:. Https:/ www.facebook.com/SuperCaelen. There are even more excitin...

caeleno.it

Caeleno srl :: Misura Semplice e diretta del potenziale fenolico delle uve

ALCYONE PM-03 Polyphenolic Meter. Il nuovo apparecchio portatile brevettato dalla ditta CAELENO srl, specializzata in progetti di sviluppo e controllo di processo dal grappolo d’uva al vino, determina in pochi secondi il potenziale polifenolico della buccia. Il ALCYONE PM-03 è molto semplice da usare: basta schiacciare l’acino in modo da togliere la polpa e i vinaccioli e porre la buccia nella pinza.

caelenquest.blogspot.com

Caelen's Quest

A test of faith and courage. How You Can Help. Jan 2014 - 10 mths old. The first time C visited the Zoo was 1.5 years ago. Too young to remember anything. It was more of a must-visit-the-zoo-before-he-turns-one affair. Last Saturday, we brought C there again. It was meant to be an educational trip. We thought he would be happy to see and name the animals he came to know through books and YouTube. It was also one of his very few trips out of the house in recent months. Jun 2015 - 2 yrs old. Via milk pump&...

caelenrocks.com

Home - Caelen's Site

Welcome to Caelen Rocks!

caelenscause.org

Caelen's Cause | Dedicated to helping families in the NICU

Dedicated to helping families in the NICU. Caelen James Thom was born at Carolinas Medical Center on June 23, 2012. Due to a series of complications he spent the next 155 days of his life in the Levine Children’s Hospital Neonatal Intensive Care Nursery. The West Nursery became a second home for my family during his stay. In an odd way it actually became comforting to be there, as we knew he had access to the very best medical staff.