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Hope For Mattie | Everyday holds the possibility of a miracleEveryday holds the possibility of a miracle
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Everyday holds the possibility of a miracle
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Hope For Mattie | Everyday holds the possibility of a miracle | hopeformattie.com Reviews
https://hopeformattie.com
Everyday holds the possibility of a miracle
hopeformattie.com
Sponsor-A-Therapy | Hope For Mattie
https://hopeformattie.com/sponsortherapy
Everyday holds the possibility of a miracle. Skip to primary content. Steady As We Go. How Can I Help? Past Events / Fundrasiers. Hope for Mattie Jewelry. Hope for Mattie 2016 Golf Tournament. 2016 Run For Hope 5K. Our Hope for Mattie is that one day she will reach her full potential. Many of the therapies Mattie undergoes are not covered by insurance. Your support will enable Mattie to continue her therapies and one day reach her ultimate goal of walking. One ABM Therapy Session $60.
Fundraising | Hope For Mattie
https://hopeformattie.com/fundraising
Everyday holds the possibility of a miracle. Skip to primary content. Steady As We Go. How Can I Help? Past Events / Fundrasiers. Hope for Mattie Jewelry. Hope for Mattie 2016 Golf Tournament. 2016 Run For Hope 5K. And Fund-Racing for Mattie. For more details see below. We have set up a bank account and a paypal account for Mattie to accept donations/gifts (not tax-deductible). To learn more about Mattie, check out Mattie’s Story. Hope for Mattie Signature Jewelry Collection. Training for any race is not...
Hope for Mattie 2016 Golf Tournament | Hope For Mattie
https://hopeformattie.com/golf-tournament
Everyday holds the possibility of a miracle. Skip to primary content. Steady As We Go. How Can I Help? Past Events / Fundrasiers. Hope for Mattie Jewelry. Hope for Mattie 2016 Golf Tournament. 2016 Run For Hope 5K. Hope for Mattie 2016 Golf Tournament. 4th Annual Hope for Mattie Charity Golf Tournament. Saturday * October 29, 2016 * 1pm Shotgun Start. Heritage Harbor Golf and Country Club. 19502 Heritage Harbor Pkwy * Lutz, Florida * 33558. There are 2 ways to register for this event! Sponsorship Opportu...
Hope for Mattie Sponsors | Hope For Mattie
https://hopeformattie.com/sponsers
Everyday holds the possibility of a miracle. Skip to primary content. Steady As We Go. How Can I Help? Past Events / Fundrasiers. Hope for Mattie Jewelry. Hope for Mattie 2016 Golf Tournament. 2016 Run For Hope 5K. Hope for Mattie Sponsors. A HUGE thank you to all of our sponsors! Please take a moment to check these companies out! DMDesigns specializes in handmade jewelry, accessories, bath and body, gifts and home decor. Http:/ www.facebook.com/DMDesigns11. It’s Professional Design, Made Personal.
Cerebral Palsy | Hope For Mattie
https://hopeformattie.com/tag/cerebral-palsy
Everyday holds the possibility of a miracle. Skip to primary content. Skip to secondary content. Steady As We Go. How Can I Help? Past Events / Fundrasiers. Hope for Mattie Jewelry. Hope for Mattie 2016 Golf Tournament. 2016 Run For Hope 5K. Tag Archives: Cerebral Palsy. How far we have come. February 9, 2016. Yesterday at the Doctors Office. 9 Year old boy:. Why is she in a wheelchair? She was born with cerebral palsy. Her brain has a hard time telling her legs what to do. 9 Year old boy:. Mattie, Is th...
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About | Lilla isa
https://lillaisa.wordpress.com/about
Isa's journey living with epilepsy and brain malformation. Hi and welcome to Isa’s life. I’m Lizette, Isa’s mom and this is her story. I’m a Mexican born now living in Sweden, I’m married to Nicklas and we have a yoga studio in Uppsala Sweden, just so you understand if you read something about classes or the studio, this is where we spend most of our day together with Isa. If you want to read about Isa’s story, the best place to start is here “Where to begin? Lilla Isa means: Little Isa in swedish. The O...
Wordless Wednesday | Lilla isa
https://lillaisa.wordpress.com/2014/11/05/wordless-wednesday
Isa's journey living with epilepsy and brain malformation. November 5, 2014. Isa’s day care picture. 4 thoughts on “ Wordless Wednesday. November 5, 2014 at 1:55 pm. Farmors söta lilla tjej. November 5, 2014 at 7:02 pm. When I see your pictures Lizette, I admire your two wonderful girls; Ella is so cute but when I see Isa my heart opens up. I love her. November 6, 2014 at 11:06 am. Lovely charming fantastic girl . She is so Beautiful. Iza is magic. November 6, 2014 at 11:06 am. Leave a Reply Cancel reply.
lillaisa | Lilla isa
https://lillaisa.wordpress.com/author/lizmadelline
Isa's journey living with epilepsy and brain malformation. It’s been a while…. July 3, 2016. Isa is 4 1/2 years old. She has improved tremendously in every sense over this year, much more that I could have ever imagined. She has surprised us over and over again. After her intensive training with Veronika she started walking barefoot, standing up and sitting down from a chair, leaning down to pick up stuff and slowly she became quick and good at it. After a few months without medication she started sa...
Dear Ella | Lilla isa
https://lillaisa.wordpress.com/2014/11/03/dear-ella
Isa's journey living with epilepsy and brain malformation. November 3, 2014. Every time she does something new (and new things happen everyday, all the time) Nicklas and I can’t help but to look at each other and smile, and by smile I mean wide side to side smile. I’m in love, big time. 6 thoughts on “ Dear Ella. November 3, 2014 at 10:24 pm. They are both adorable. November 4, 2014 at 6:33 pm. You have no idea how much more thankful, we know how nothing is for granted and we are enjoying it so much🙂.
Lilla isa | Isa's journey living with epilepsy and brain malformation. | Page 2
https://lillaisa.wordpress.com/page/2
Isa's journey living with epilepsy and brain malformation. Shorter leg or not? August 26, 2014. When she walks and when you look at her legs it feels like the difference is more than just a few millimeters, you can see how one leg is just shorter, not just a few millimeters. The answer he had, was that as the left side of her body is weaker she doesn’t have the strength to stretch the leg completely. August 18, 2014. Isa is big, and when I say that she is big, I mean that she has grown up so much! It fee...
Shorter leg or not? | Lilla isa
https://lillaisa.wordpress.com/2014/08/26/shorter-leg-or-not
Isa's journey living with epilepsy and brain malformation. Shorter leg or not? August 26, 2014. When she walks and when you look at her legs it feels like the difference is more than just a few millimeters, you can see how one leg is just shorter, not just a few millimeters. The answer he had, was that as the left side of her body is weaker she doesn’t have the strength to stretch the leg completely. One thought on “ Shorter leg or not? August 27, 2014 at 8:15 am. Leave a Reply Cancel reply. This wasn�...
Still here… | Lilla isa
https://lillaisa.wordpress.com/2015/06/15/still-here
Isa's journey living with epilepsy and brain malformation. June 15, 2015. She can walk and take quite a few steps by herself when she is wearing her AFO’s, she can take a few shaky steps by herself when she’s barefoot. Everything has been improving, slowly, but improving. She has just today started a 2 week intensive training with the conductive pedagogy method. We are hoping to see a lot of changes and see Isa develop in many ways during this summer months. 2 thoughts on “ Still here…. Just another Word...
Going private | Lilla isa
https://lillaisa.wordpress.com/2014/11/09/going-private
Isa's journey living with epilepsy and brain malformation. November 9, 2014. If you want to read about Isa and follow this blog, please leave a comment with your email or your username on wordpress so I can add you to the list of readers. It is only by invitation that this blog is gonna be visible. All the best from us to you. 15 thoughts on “ Going private. November 9, 2014 at 5:32 pm. Fondly, Nina (Lauren’s Mom) nm25@comcast.net. November 13, 2014 at 7:05 am. November 9, 2014 at 5:54 pm. I tried making...
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Index of /
Hope For Mark: Daily Updates
Hope For Mark: Daily Updates. Constant updates on the recovery process for Mark Logan. Subscribe by email below. Thursday, July 19, 2012. Monday, July 2, 2012. Friday, June 15, 2012. Celebrating his 85th year! I mean, 58th! Wednesday, June 13, 2012. Things are progressing faster than I can document! With his birthday this friday and fathers day sunday, there's plenty to celebrate. I hope you all will give him a call, send a card or something friday to celebrate with us. Monday, June 11, 2012. A time to p...
Jeff & Cheryl Scruggs – Hope Matters Marriage Ministries
Top Ten List for Wives. Top Ten List for Husbands. I Do Again by Jeff and Cheryl Scruggs. An attractive young couple, Jeff and Cheryl Scruggs seemed to have it all: professional success, adorable twin daughters, and a good marriage. But their picture-perfect image concealed a widening chasm between two people unable to connect on an intimate, soul-deep level. Ten disappointing years of marriage. Seven painful years of divorce. One remarkable, true-life story of a love rescued by God. About Jeff and Cheryl.
Domain pending ICANN verification.
This domain name is pending ICANN verification. Welcome to hopeformation.com Domain name registered by 123Reg/Webfusion. Please be advised that as of the 1st January 2014 it has now become a mandatory requirement from the Internet Corporation for Assigned Name and Numbers (ICANN) that all ICANN accredited registrars verify the WHOIS contact information for all new domain registrations, domain transfers and registrant contact modifications. Why has this domain been suspended? If you have not received the ...
Matt's Hope
This blog is set up to provide information about fund raising activities for Matt. What is Matts Hope? Wednesday, June 1, 2011. I know I have not updated this blog and there are a lot of updates. Until I can do a more in-depth update I will just post this quick one. The donation jars have brought in a few hundred dollars. Thank you to everyone who has donated through these jars around town! Matt is healing very very well! I will try to post more details when I can. It is difficult for me as I live wi...
Hope For Mattie | Everyday holds the possibility of a miracle
Everyday holds the possibility of a miracle. Skip to primary content. Skip to secondary content. Steady As We Go. How Can I Help? Past Events / Fundrasiers. 2016 Run For Hope 5K. Hope for Mattie 2017 Charity Golf Tournament. Rolling with the rest of us. October 6, 2017. Today is World Cerebral Palsy Day. I am here, walking my lap. I am here, using my special grocery cart. I am here, heading to the beach. I am here, jumping in muddy puddles. I am here, finding Easter eggs. I am here, swinging on a swing.
Hope for Max and Alex
Hope for Max and Alex. October 29, 2016. Summer 2016 Beginning to End. I gotta tell you I am not quite sure what happened to this summer. There were quite a few differences from previous and some additional High family chaos, which has resulted in the synopsis vs. the day to day update. What was good, even great, about this summer? Well, it was the first summer in two years that Aaron was home for the WHOLE summer! Maybe To me, it is one more appointment that only brings us possibly dismal information wi...
HOPE FOR MAX GARCIA | Help Fight Hirschprung’s Disease
HOPE FOR MAX GARCIA. Help Fight Hirschprung’s Disease. Skip to primary content. Skip to secondary content. Max’s Surgery at Cincinnati Children’s. May 27, 2013. Flying home was interesting with TPN but we did it and we did it well. I was blessed to have good people sitting next to us on the plane ride home. Max was so well behaved and did not even notice he had his TPN. I had to go thru more security but it was all okay. After we got home we started the next phase for recovery; DILATIONS. August 9, 2012.
HOPE FOR MAZEY
Friday, August 27, 2010. 16 years 1 year and counting. Oday is not only the anniversary of our marriage, it is also the one year anniversary of our papers being approved in Colombia. So we officially have been "waiting" for our children for one year. We are happy about that. Every day that goes by brings us one day closer to holding them in our arms. We can't wait! Saturday, June 12, 2010. Friday, April 9, 2010. Ome exciting news about Jeremy's business. Enigma Productions. Aaron (Jeremy's busine...Grate...
Hope for McKenna
Wednesday, November 2, 2011. Why am I telling you all this? I want to share with you one of the little videos that was taken of McKenna while we visited. This will allow you to see her improvements from her cleft lip and cleft palate surgeries. It will also allow you to hear a little bit of her speech and understand that this next step is a necessary one. To purchase items to support McKenna. Https:/ www.facebook.com/KennasKornerBowtique. Saturday, October 22, 2011. It Means So Much To Us! August was a s...
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