myangelisabella.blogspot.com myangelisabella.blogspot.com

myangelisabella.blogspot.com

My Angel Isabella

my journey into raising a daughter with special needs

http://myangelisabella.blogspot.com/

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My Angel Isabella | myangelisabella.blogspot.com Reviews
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my journey into raising a daughter with special needs
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1 my angel isabella
2 about me
3 world urbanista
4 blog archive
5 my daily prayer
6 october
7 followers
8 posts by category
9 the emotional journey
10 family stories
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my angel isabella,about me,world urbanista,blog archive,my daily prayer,october,followers,posts by category,the emotional journey,family stories,development,blogs with videos,all things medical,isabella being isabella,birth history,keeping the faith,amen
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My Angel Isabella | myangelisabella.blogspot.com Reviews

https://myangelisabella.blogspot.com

my journey into raising a daughter with special needs

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myangelisabella.blogspot.com myangelisabella.blogspot.com
1

My Angel Isabella: March 2014

http://myangelisabella.blogspot.com/2014_03_01_archive.html

My journey into raising a daughter with special needs. View my complete profile. This is for WHS Mommies too. Friday, March 21, 2014. This is for WHS Mommies too. Found this video, "Dear Future Mum",. Made for World Down Syndrome Awareness Day. It's message hold's true for us too, the parents of individuals with Wolf Hirschhorn Syndrome,. Most especially to the new mommies and the mommies to be of children with 4p minus. I really hope this video finds you. It will give you HOPE! Labels: blogs with videos.

2

My Angel Isabella: April 2011

http://myangelisabella.blogspot.com/2011_04_01_archive.html

My journey into raising a daughter with special needs. View my complete profile. Monday, April 25, 2011. Here is a video my son booing his sister. Pardon the "W" sitting as I did not want to interrupt their happy moment. Wednesday, April 06, 2011. 8220;Your life must have changed after having been given a child with special needs”. Someone told me once… and yes, I may have to say so that my life has indeed changed. But doesn’t every baby, special or not change you in a way? And, yeah, we don’t real...

3

My Angel Isabella: April 2012

http://myangelisabella.blogspot.com/2012_04_01_archive.html

My journey into raising a daughter with special needs. View my complete profile. Saturday, April 07, 2012. Labels: blogs with videos. At 28 months, Isay now weighs about 20 lbs. and I finally put away all of her 6 to 9 month clothes. YAY! There seems to be a slowing down on her weight gain, yes in spite of all the cream and butter we've added to her diet. It could be because she has been more physically active, and thus, burning more calories. And yes, this is why she is burning more calories! When her b...

4

My Angel Isabella: This is for WHS Mommies too

http://myangelisabella.blogspot.com/2014/03/this-is-for-us-whs-mommies.html

My journey into raising a daughter with special needs. View my complete profile. This is for WHS Mommies too. Friday, March 21, 2014. This is for WHS Mommies too. Found this video, "Dear Future Mum",. Made for World Down Syndrome Awareness Day. It's message hold's true for us too, the parents of individuals with Wolf Hirschhorn Syndrome,. Most especially to the new mommies and the mommies to be of children with 4p minus. I really hope this video finds you. It will give you HOPE! Labels: blogs with videos.

5

My Angel Isabella: July 2012

http://myangelisabella.blogspot.com/2012_07_01_archive.html

My journey into raising a daughter with special needs. View my complete profile. Isabella: Summer 2012 Update. Ah-uh Yes and Ah-uh No. Apparently, It’s All About Her. Sunday, July 29, 2012. Isabella: Summer 2012 Update. Here is a long overdue update on how my little Isabella has been doing…. In May 2012 Isabella weighed in at 21 lbs and 29 inches. No wonder our backs were already hurting, she got so heavy, she slips down from my arms from all that weight. For that blog post. Isay with her"chunky" legs.

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Go, Ty! Go!: The Great Television Turnoff

http://gotygo.blogspot.com/2012/11/the-great-television-turnoff.html

The events of our life from my perspective. Inspired by a little boy. Friday, November 30, 2012. The Great Television Turnoff. Imagine my surprise when Peyton informs me he wants an iPhone for Christmas. Me too, kid. He's 7. What the heck does he need an iPhone for? Subscribe to: Post Comments (Atom). There was an error in this gadget. The Great Television Turnoff. Simple template. Template images by MadCircles.

ourlittledillpickle.blogspot.com ourlittledillpickle.blogspot.com

Our Little Pickle: May 2012

http://ourlittledillpickle.blogspot.com/2012_05_01_archive.html

Wednesday, May 16, 2012. A dose of reality. This scared me to death and to be honest it made me think, "is this going to be the horrible seizure that takes him from us? It reminded me how fragile Dylan really is and it made me sad. I was once again asking, "why did this happen? Why did our child get diagnosed with this rare syndrome? Subscribe to: Posts (Atom). Make a donation directly to Dylan's trust. To read about Dylan's medical diagnosis click HERE. A dose of reality. View my complete profile.

4karlysworld.blogspot.com 4karlysworld.blogspot.com

Karly's World: Busy Days...And Make a Wish Update!

http://4karlysworld.blogspot.com/2010/03/busy-daysand-make-wish-update.html

This blog is to keep family and friends updated on the things going on in Karly's World. Karly is our daughter who was diagnosed with Wolf Hirschorn Syndrome (4P-). She is 5 years old and is such a loveable little girl. Busy Days.And Make a Wish Update! PA, United States. View my complete profile. Monday, March 22, 2010. Busy Days.And Make a Wish Update! Another day at the park! Happy as can be. Ethan met this favorite Hershey Bears player last night. Autograph and all. March 22, 2010 at 2:01 PM.

4karlysworld.blogspot.com 4karlysworld.blogspot.com

Karly's World: February 2011

http://4karlysworld.blogspot.com/2011_02_01_archive.html

This blog is to keep family and friends updated on the things going on in Karly's World. Karly is our daughter who was diagnosed with Wolf Hirschorn Syndrome (4P-). She is 5 years old and is such a loveable little girl. Some of my favorites. PA, United States. View my complete profile. Wednesday, February 16, 2011. Some of my favorites. Karly riding rides at Hershey Park this past summer. Hershey, PA Home of the 2014 4P- Support Group National Conference! Family Time at PENN STATE! No need to say anymore.

4karlysworld.blogspot.com 4karlysworld.blogspot.com

Karly's World: Life...

http://4karlysworld.blogspot.com/2011/03/life.html

This blog is to keep family and friends updated on the things going on in Karly's World. Karly is our daughter who was diagnosed with Wolf Hirschorn Syndrome (4P-). She is 5 years old and is such a loveable little girl. PA, United States. I am the proud mom of Ethan (9 yrs. old) and Karly (5 yrs old). My wonderful husband is Jim and we have been married for 6 years. Karly is our special little girl. She has Wolf-Hirschhorn Syndrome (WHS) an extremely rare chromosome disorder. View my complete profile.

gotygo.blogspot.com gotygo.blogspot.com

Go, Ty! Go!: Home

http://gotygo.blogspot.com/2012/11/home.html

The events of our life from my perspective. Inspired by a little boy. Thursday, November 29, 2012. Paperwork, paperwork, and more paperwork. That is the name of the game right now. The case worker is coming next week for our first home visit. We are also working on a portfolio of our family for birth moms to view. They encouraged us to add a video or dvd for them to get a better feel for our family so I put together a slideshow. Here is the finished product:. December 5, 2012 at 6:36 PM.

gotygo.blogspot.com gotygo.blogspot.com

Go, Ty! Go!: August 2012

http://gotygo.blogspot.com/2012_08_01_archive.html

The events of our life from my perspective. Inspired by a little boy. Tuesday, August 14, 2012. First trip to the Zoo. Ready to see the animals! Monday, August 6, 2012. The Coffey's are home. Sunday, August 5, 2012. The results are in (again). Feeling better and ready to play. He is Olympic training always stretch before your workout! Saturday, August 4, 2012. Tyler wakes up from his nap and is fussy and hot. I take his temperature and it's 100. I give him some Tylenol. We go over options and decide on t...

gotygo.blogspot.com gotygo.blogspot.com

Go, Ty! Go!: January 2013

http://gotygo.blogspot.com/2013_01_01_archive.html

The events of our life from my perspective. Inspired by a little boy. Wednesday, January 16, 2013. It's 2013. Shouldn't we be riding around in flying cars by now? Ty and Daddy at Riley. Brian and I attended his annual kickoff event in Louisville this past weekend. For me, it always fun to get dressed up and hang out with adults for a change! Brian and his team. Tyler is overall in good health and we are excited what this new year will bring for Team Coffey. Subscribe to: Posts (Atom).

4karlysworld.blogspot.com 4karlysworld.blogspot.com

Karly's World: March 2011

http://4karlysworld.blogspot.com/2011_03_01_archive.html

This blog is to keep family and friends updated on the things going on in Karly's World. Karly is our daughter who was diagnosed with Wolf Hirschorn Syndrome (4P-). She is 5 years old and is such a loveable little girl. PA, United States. I am the proud mom of Ethan (9 yrs. old) and Karly (5 yrs old). My wonderful husband is Jim and we have been married for 6 years. Karly is our special little girl. She has Wolf-Hirschhorn Syndrome (WHS) an extremely rare chromosome disorder. View my complete profile.

4karlysworld.blogspot.com 4karlysworld.blogspot.com

Karly's World: Finally I blog...

http://4karlysworld.blogspot.com/2010/07/finally-i-blog.html

This blog is to keep family and friends updated on the things going on in Karly's World. Karly is our daughter who was diagnosed with Wolf Hirschorn Syndrome (4P-). She is 5 years old and is such a loveable little girl. PA, United States. I am the proud mom of Ethan (9 yrs. old) and Karly (5 yrs old). My wonderful husband is Jim and we have been married for 6 years. Karly is our special little girl. She has Wolf-Hirschhorn Syndrome (WHS) an extremely rare chromosome disorder. View my complete profile.

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Saturday, February 11, 2012. What do you think? I just purchased this dress from Stella McCartney's Fall 2003 collection and I was planning to wear it to an event next weekend, but I don't know which shoes I should wear with it. It can be anything; I just need some suggestions, as I am the worst at matching shoes to outfits, or rather outfits to shoes. The dress is much more vibrant than in this photo, the lighting on the runway must have been dark. It is a teal green with accents of black and silver.

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My Angel Isabella

My journey into raising a daughter with special needs. View my complete profile. This is for WHS Mommies too. Friday, March 21, 2014. This is for WHS Mommies too. Found this video, "Dear Future Mum",. Made for World Down Syndrome Awareness Day. It's message hold's true for us too, the parents of individuals with Wolf Hirschhorn Syndrome,. Most especially to the new mommies and the mommies to be of children with 4p minus. I really hope this video finds you. It will give you HOPE! Labels: blogs with videos.

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