fightingforlizzy-nina blogspot.com

Lizzys Page - Living with Spinal Muscular Atrophy

Lizzys Page - Living with Spinal Muscular Atrophy. All about Lizzys life and my life as Lizzys caregiver. Lizzy has Spinal Muscular Atrophy Type 1 and is a miracle! She has NEVER been able to stand, walk or sitwith out assistance. She is such an amazing child with the determination to over come many of her battles with this terrible disease. She is a happy child and is always smiling. Wednesday, January 14, 2015. Dealing with so many deaths to people that were so close to me is the hardest thing I h.

OVERVIEW

This web page fightingforlizzy-nina.blogspot.com currently has a traffic ranking of zero (the lower the superior). We have explored nineteen pages inside the domain fightingforlizzy-nina.blogspot.com and found two hundred and fifty-four websites referring to fightingforlizzy-nina.blogspot.com.
Pages Crawled
19
Links to this site
254

FIGHTINGFORLIZZY-NINA.BLOGSPOT.COM RANKINGS

This web page fightingforlizzy-nina.blogspot.com has seen a fluctuation levels of traffic within the past the year.
Traffic for fightingforlizzy-nina.blogspot.com

Date Range

1 week
1 month
3 months
This Year
Last Year
All time
Traffic ranking (by month) for fightingforlizzy-nina.blogspot.com

Date Range

All time
This Year
Last Year
Traffic ranking by day of the week for fightingforlizzy-nina.blogspot.com

Date Range

All time
This Year
Last Year
Last Month

LINKS TO WEB SITE

Kaitlyn Hatchard Spinal Muscular Atrophy-Type 1

My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, swallow and clear my airway. Tuesday, August 21, 2012. So what can we do about this? Our other biggest battle h.

Skylars Journeys a boys battle with SMA

Its not by what you have that makes you happy, but by who is in your life that truly makes you happy. Saturday, April 04, 2015. 10 years old and oh so cute! Links to this post. Monday, March 30, 2015. Almost 10 just a few more days. We recently bought Sky a new van. So look out spring and summer were coming for YA! Links to this post.

Brynlees Battle with SMA

Tuesday, January 17, 2012. Where do I begin? A couple days after she died her nurse called me. They said no matter what she would have died soon anyway. Even hearing that I still blame myself. I go over that day all the time and it still hurts. Thursday, June 9, 2011. August 29, 2007 June 06, 2011.

Helping Kai Play

Monday, October 10, 2011. Birthday and walk around 5 years old. These were my goals for Kai. Kai was going to crawl and walk. I was sure of it. He was just going to be farther behind the curve than most kids. We began weekly therapy visits and I worked with Kai every day I could.

нормальная жизнь глазами инвалида

Поздравляю товарищей по сообществу с наступившим уже новым годом! Традиционно - желаю, чтобы все любимое в этом году у вас получилось собрать вместе не только на картинке. И наилучшим и наиприятнейшим для вас образом.

My Princess Danielle

A little life transforming many lives. Sunday, November 27, 2016. Eye stye go away . Danielle had this eye stye in her left eye for months. At one point of time both eye got infected. Few week later we notice the eye stye was gone. keeping finger cross that it will not come back. EYE STYE DONT COME BACK! Links to this post. Friday, September 16, 2016.

Something More to Life

Thursday, September 11, 2014. I go in waves you could say. My daughter graduated from High School. I am very proud of her and the accomplishments we achieved while in MHS. She has grown into a very beautiful, smart and caring woman! Fast forward to today. Time will tell what the future holds for us. Wednesday, March 12, 2014. Where is YOUR mind? .

Caelens Quest

A test of faith and courage. Jan 2014 - 10 mths old. The first time C visited the Zoo was 1. 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.

Clemons Family

Monday, January 9, 2017. You are always in a hurry. Monday, January 2, 2017. Christmas break was filled with lots of fun. So sad it is over. Fun to not have anywhere to go and just do whatever we want. Well, almost the fam. This is Nick at Boulton. Then we decided to go to Texas Roadhouse after sledding. Nothing like the Awesome Blossom. Nick caught that T shirt and Jack caught that Stars Ball. She did such a great job. Here we all are! Where to begin.

WHAT DOES FIGHTINGFORLIZZY-NINA.BLOGSPOT.COM LOOK LIKE?

Desktop Screenshot of fightingforlizzy-nina.blogspot.com Mobile Screenshot of fightingforlizzy-nina.blogspot.com Tablet Screenshot of fightingforlizzy-nina.blogspot.com

FIGHTINGFORLIZZY-NINA.BLOGSPOT.COM HOST

Our parsers identified that a lone page on fightingforlizzy-nina.blogspot.com took zero milliseconds to come up. We could not find a SSL certificate, so our crawlers consider fightingforlizzy-nina.blogspot.com not secure.
Load time
0 secs
SSL
NOT SECURE
Internet Protocol
216.58.219.225

WEBSITE IMAGE

SERVER OS AND ENCODING

I found that this domain is operating the GSE server.

PAGE TITLE

Lizzys Page - Living with Spinal Muscular Atrophy

DESCRIPTION

Lizzys Page - Living with Spinal Muscular Atrophy. All about Lizzys life and my life as Lizzys caregiver. Lizzy has Spinal Muscular Atrophy Type 1 and is a miracle! She has NEVER been able to stand, walk or sitwith out assistance. She is such an amazing child with the determination to over come many of her battles with this terrible disease. She is a happy child and is always smiling. Wednesday, January 14, 2015. Dealing with so many deaths to people that were so close to me is the hardest thing I h.

CONTENT

This web page fightingforlizzy-nina.blogspot.com states the following, "Lizzys Page - Living with Spinal Muscular Atrophy." We saw that the webpage said " All about Lizzys life and my life as Lizzys caregiver." It also said " Lizzy has Spinal Muscular Atrophy Type 1 and is a miracle! She has NEVER been able to stand, walk or sitwith out assistance. She is such an amazing child with the determination to over come many of her battles with this terrible disease. She is a happy child and is always smiling. Wednesday, January 14, 2015. Dealing with so many deaths to people that were so close to me is the hardest thing I h."

SEEK SIMILAR DOMAINS

Fighting for Maia

Tuesday, January 14, 2014. Wednesday, October 2, 2013. Wednesday, August 14, 2013. This Saturday I face my.

Fighting For Mike

Mike Metzler, loving husband, father and grandfather, is fighting a Stage 4 battle with cancer. Tuesday, September 2, 2008. 58, of 1837 Gabler. PA, went to be with the Lord on Sunday, August 31, 2008, at his home. Born Sunday, December 18, 1949, in Altoona. PA, he was the son of the late Paul F. And the late Irene A. And associate member of the V.

Fighting for my Children

I am a mother of two high functioning autistic children,age 15 and 16. Monday, March 30, 2015. Sunday, December 22, 2013. Everything is good in this autism house. The kids are teens, what else can I say. When I say do this they say no way. I stick to my word and they usually come through after a meltdown or two. Merry Christmas to you and a peaceful time too. Wednesday, October 10, 2012.

Fighting For My Free Spirit

Tuesday, July 26, 2011. holy moly! A lot has happened. I have had an internal attitude towards my blog. I am back in W.

Fighting for Nippon

Japanese Pop Culture Straight To Your Browser. Anime Subtitles Can Be Pretty Bad Too. Anime Subtitles Can Be Pretty Bad Too. Screw Griffith, The Good Points of this Berserk Character. Anime Subtitles Can Be Pretty Bad Too.