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Hope For HunterOur cleft journey from the very beginning
http://hope4hunter.blogspot.com/
Our cleft journey from the very beginning
http://hope4hunter.blogspot.com/
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Our cleft journey from the very beginning
hope4hunter.blogspot.com
Hope For Hunter: August 2011
http://hope4hunter.blogspot.com/2011_08_01_archive.html
Our cleft journey from the very beginning. Monday, August 22, 2011. Going to have a baby! Well he finally got the damn thing in and it didn't take too long for me to start to feel better. By this point I was off the external monitors and all of the monitors for the contractions and Hunters heart rate were coming right from the source. Hurry up and wait! I was so glad that all of my family was there. My mom, Dad, Sister, Husband (Josh), and for a good portion of time, my son, Avery. Daddy and Big Brother!
Hope For Hunter: August 2012
http://hope4hunter.blogspot.com/2012_08_01_archive.html
Our cleft journey from the very beginning. Saturday, August 25, 2012. Sorry :( I'm a crappy blogger! Well, I'm officially admitting that I suck at staying up to date on this. I really wish I was more committed to making time to update here. But, I will do my best and that's the best I can do, right? He is a very happy, healthy baby. This was the day after his Palate Surgery. Still a bit groggy, but ready to get moving! Trying to find ways to get those arm restraints off! Believe it or not, That's a SMILE!
Hope For Hunter: November 2011
http://hope4hunter.blogspot.com/2011_11_01_archive.html
Our cleft journey from the very beginning. Friday, November 18, 2011. Doin' The NAM Thing. Okay, so, I admit I am WAY late on this post. Tough cookies - read on! On Aug. 31st Hunter got his NAM ( Nasoalveolar Molding Device. Was added to his NAM. This part with help shape his nose to hopefully give it a more semetrical look after surgery. There's not too much to SAY about the NAM - other than the fact that it truly is AMAZING. . . I'll just let you see for yourself in the following pictures.
Hope For Hunter: April 2011
http://hope4hunter.blogspot.com/2011_04_01_archive.html
Our cleft journey from the very beginning. Tuesday, April 26, 2011. This blog is for our friends and family. It is intended to help them follow our journey as we become acquainted with our newest addition: Hunter John. We will not only become a mother, a father, and a brother, a grandma, a grandpa, and an aunt, of a baby born with cleft lip and cleft palate, but we will become stronger, closer, and complete as a family. Our journey begins with finding out the big news: We were pregnant! The ultrasound te...
Hope For Hunter: I do declare, "A Lip Repair!"
http://hope4hunter.blogspot.com/2011/12/i-do-declare-lip-repair.html
Our cleft journey from the very beginning. Thursday, December 29, 2011. I do declare, "A Lip Repair! Well, I pushed this post off until the very last minute didn't I? On Dec. 6th., Hunter went to the hospital for his lip repair surgery! As the days were closing in on the repair my stomach just kept churning and I would just stare at him and soak him in! A smile to remember. 65279;. Back in my arms. 65279;. 65279;. 65279;. The day after surgery and smiling already! A Video for Hunter. Hey, f...
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theserthedaysofourlives.blogspot.com
These are the Days of Our Lives: Sept is Craniofacial Acceptance Month
http://theserthedaysofourlives.blogspot.com/2011/09/sept-is-craniofacial-acceptance-month.html
These are the Days of Our Lives. This is the story of our crazy, hectic days! Thursday, September 1, 2011. Sept is Craniofacial Acceptance Month. September is Craniofacial Acceptance Month! I guess I prefer Awareness to Acceptance, or Craniofacial Education Month would be even better, but whatever the title, the point is to educate others. So thought I would educate the 2 people who may read this ; ) Feb. '09 my son was born with an incomplete bilateral cleft lip. This was a. We also have feelings! So if...
theserthedaysofourlives.blogspot.com
These are the Days of Our Lives: Appointment with the Development Pediatrician
http://theserthedaysofourlives.blogspot.com/2011/08/developmental-pediatrian-appointment.html
These are the Days of Our Lives. This is the story of our crazy, hectic days! Friday, August 26, 2011. Appointment with the Development Pediatrician. Today has been a loonnggg day. We left at 8am to get to the appointment at 9, then we waited and waited and waited some more. Finally, over an hour late the Dr. came in! Subscribe to: Post Comments (Atom). I'm a work from home mom to 4 bio and 3 step kids ranging in age from 2-19! Between taking care of kids and our nursery I stay pretty busy!
theserthedaysofourlives.blogspot.com
These are the Days of Our Lives: September 2011
http://theserthedaysofourlives.blogspot.com/2011_09_01_archive.html
These are the Days of Our Lives. This is the story of our crazy, hectic days! Thursday, September 1, 2011. Sept is Craniofacial Acceptance Month. September is Craniofacial Acceptance Month! I guess I prefer Awareness to Acceptance, or Craniofacial Education Month would be even better, but whatever the title, the point is to educate others. So thought I would educate the 2 people who may read this ; ) Feb. '09 my son was born with an incomplete bilateral cleft lip. This was a. We also have feelings! So if...
theserthedaysofourlives.blogspot.com
These are the Days of Our Lives: August 2011
http://theserthedaysofourlives.blogspot.com/2011_08_01_archive.html
These are the Days of Our Lives. This is the story of our crazy, hectic days! Friday, August 26, 2011. Appointment with the Development Pediatrician. Today has been a loonnggg day. We left at 8am to get to the appointment at 9, then we waited and waited and waited some more. Finally, over an hour late the Dr. came in! Thursday, August 25, 2011. Busy, busy days. I decided to start this blog because there is just so much going on! For starters it's T1's first week of college! K seems to like her teachers t...
theserthedaysofourlives.blogspot.com
These are the Days of Our Lives: Busy, busy days
http://theserthedaysofourlives.blogspot.com/2011/08/busy-busy-days.html
These are the Days of Our Lives. This is the story of our crazy, hectic days! Thursday, August 25, 2011. Busy, busy days. I decided to start this blog because there is just so much going on! For starters it's T1's first week of college! This is T2's last year in middle school, next year she will be moving to the high school! She is cheer captain this year and as captain she has to call the cheers! Not even gummy snacks which are his favorite! IDK how to help him since I have to feed him at home. I ju...
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Hope for Humans - Caring for Children with Nodding Syndrome - Hope For Humans
I want to help. Hope for Humans exists to provide dignity, comfort, safety and hope to children afflicted with Nodding Syndrome and their families. We are creating a future where these innocent victims can receive the lifelong medical care and support they need to live a dignified life. We're dedicated to the treatment and eradication of this devastating and fatal condition. Share this website with a friend. Our goal is to create replicable models of comprehensive care and. Be in Kitgum province.
Hope4Hungary
Ldquo; I don’t know where, I don’t know how, I don’t know when, but here I amI want to be baptized”. More What's New . . . Bull; Hungarian History. Bull; Team Leaders. Bull; Volunteer Guide. Bull; Special Testimony. Western Hungary Team Website 2016.
hope4hungary.net
hope4hungary.org
Hope For Hunter
Our cleft journey from the very beginning. Saturday, August 25, 2012. Sorry :( I'm a crappy blogger! Well, I'm officially admitting that I suck at staying up to date on this. I really wish I was more committed to making time to update here. But, I will do my best and that's the best I can do, right? He is a very happy, healthy baby. This was the day after his Palate Surgery. Still a bit groggy, but ready to get moving! Trying to find ways to get those arm restraints off! Believe it or not, That's a SMILE!
Hope 4 Hunter
What is MPS II? Spotlight Child of the Month. What is MPS II? Spotlight Child of the Month. Learn more about MPS II. What is Hope 4 Hunter? What is MPS II. MPS II is a rare genetic disease that affects just 2,000 people world-wide, mostly boys. What is Hope 4 Hunter. Hope 4 Hunter is dedicated to finding a cure for MPS II and improving the lives of all those affected by this catastrophic disease. How do I get involved? There are many ways to get involved with Hope 4 Hunter…. Spotlight Child of the Month.
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Where there is no counsel, the people fall; But in the multitude of counselors there is. The Hope For Hurting Families Ministry meets every Thursday evening @ 730pm at Evangel Cathedral in Upper. Marlboro, MD. There is no obstacle too great for God. We are here to serve, let Hope Ministries help you! HOPE Phone No.: 240-232-2049 * * * * * * * * * * * * * *. Have you accepted Jesus as your Lord and savior? Would you like to reap all the benefits that being a Child of God. Hope for Hurting Families, Inc.
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Why NOT Couples Counseling? MOSAIC DV THREAT ASSESSMENT. Characteristics of an Abuser. Safety Planning with Children of Battered Women. The Unheard: Men DV Victims. Free from Verbal Abuse FORUM. DV Among the Upper Class. Dispelling Top DV/IPV Myths. Children of Domestic Violence. Nationwide Adult Survivor Recovery Groups for Every State. Adult Survivor Groups for every state. National Association of Adult Survivors of Child Abuse. Addiction and Recovery in the Church. Effects of Addiction on Children.
Hope 4 Hurting Kids - Moving from hurt and trauma to Hope and Healing.
Child Abuse & Neglect Help Center. Cutting and Self-Harm Help Center. Divorce and Modern Family Help Center. Domestic Violence Help Center. Family Issues Help Center. Foster Families Help Center. Sexual Abuse and Rape Help Center. Substance Abuse Help Center. Children of Divorced/Separated Parents. Child Abuse & Neglect Help Center. Cutting and Self-Harm Help Center. Divorce and Modern Family Help Center. Domestic Violence Help Center. Family Issues Help Center. Foster Families Help Center. March 29, 2018.
