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Noah's ArkOur Journey: Knowing, Loving, Losing & Remembering Noah
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Our Journey: Knowing, Loving, Losing & Remembering Noah
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Our Journey: Knowing, Loving, Losing & Remembering Noah
Noah's Ark: Reflections On The Year Gone By
http://noahsarkperth.blogspot.com/2011/11/reflections-on-year-gone-by.html
Our Journey: Knowing, Loving, Losing and Remembering Noah. Thursday, November 17, 2011. Reflections On The Year Gone By. And what a test the past year has been. I have come to realise that the things in life that can bring you the most joy can also, on the other hand, bring you the most agonising heartbreaking pain. It's just the way it is in life. There are no immediate answers to the "whys", that we ask ourselves when trying to deal with this type of tragedy. "Why did this happen"? Kat and Aaron Reed.
Noah's Ark: Heartfelt
http://noahsarkperth.blogspot.com/2012/03/heartfelt.html
Our Journey: Knowing, Loving, Losing and Remembering Noah. Wednesday, March 21, 2012. Https:/ www.facebook.com/Heartfelt.Australia. Http:/ www.heartfelt.org.au/. I had wanted to have some professional shots of Noah done but I didn't know if a regular photographer would be comfortable or be able to work within our circumstances. I contacted Heartfelt and that was when we first met the lovely and talented Deanna Whyte, from Deanna Whyte Photography. These are some of my favourites. I thought I would add a ...
Noah's Ark: Kids Just Wanna Have Fun
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Our Journey: Knowing, Loving, Losing and Remembering Noah. Monday, July 23, 2012. Kids Just Wanna Have Fun. Children seem to have such a limitless imagination and creative process. I find it so amazing just to watch a child and how they interact. I love to listen to the way they express themselves and the somewhat random, but often philosophical comments they make. So how then do you nourish creativity and help a child express what their body is sometimes unable to? I am constantly searching for new acti...
Noah's Ark: October 2012
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Our Journey: Knowing, Loving, Losing and Remembering Noah. Tuesday, October 2, 2012. Up, Up and Away Little Buddy. For those family, friends and followers of our journey whom may not yet have heard,. Noah peacefully took his last breath this past Friday, September 28th at 11:52am. He inspired so much in his short 22 months. I am forever grateful. Thank you Noah xoxo. Kat and Aaron Reed. Subscribe to: Posts (Atom). Welcome To Noahs Ark. On September 28th 2012, we said goodbye to our little buddy.
Noah's Ark: Starlight Star Bright
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Our Journey: Knowing, Loving, Losing and Remembering Noah. Friday, May 3, 2013. Being that today is Starlight Day I thought I'd share our experience and encourage people to give a little. Starlight help to brighten the lives of seriously sick kids and their families, at a time when illness, hospitals and intensely difficult situations have become the norm. It gave us something to plan and look forward to. Something about the future we could smile about. Our trip was booked for the end of October. I find ...
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Joshua's Story: October 2013
http://amazingjoshua.blogspot.com/2013_10_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Monday, October 14, 2013. Serial Casting (No Botox for Joshua.Again). So, today we once again saw the Visiting Paediatric Rehabilitation team from Adelaide. At our last appointment 3 months ago, it was recommended that Joshua have Botox injections. They offered to do it that very next day, but I elected to wait three months until the clinic this week. Over the past three months we have seen a ...
Joshua's Story: Joshua's Developmental Milestones
http://amazingjoshua.blogspot.com/p/joshuas-developmental-milestones.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Smile: 4 weeks but consistently from 7 weeks. Laugh: 8 weeks but consistently from 12 weeks. Rolled from Back: 4 months. Rolled from Stomach: 4 months but only did it twice until 8.5 months when he started doing it regularly. Rested on Elbows: 5 months. Rocked on Hands and Knees: 9-10 months. Moved into Sitting position:. Crawled: Army Crawled- 11.5 months. Pulled to Kneeling: 13 months. The C...
Joshua's Story: June 2013
http://amazingjoshua.blogspot.com/2013_06_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Thursday, June 6, 2013. The Technical Talk from Joshua's Appointment. I got a copy of the letter today that the Rehab Doctor from the visiting clinic sends to Joshua's Paediatrician. I never did get a copy of the one from his last rehab appointment, so I am going to ask his Paed for a copy next time we see him, cos I really like getting the goss. LOL. So the letter says:. Tuesday, June 4, 2013.
Joshua's Story: August 2013
http://amazingjoshua.blogspot.com/2013_08_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Friday, August 2, 2013. Thinking about the future. So, today I had to go to a meeting with Joshua's Occupational Therapist and Physiotherapist to have a goal setting/planning meeting. I wrote down a list of goals for him and took it with me. They were all short term goals. I want him doing things that are age appropriate. He does know a few things, but definitely not to the level he should.
Joshua's Story: May 2013
http://amazingjoshua.blogspot.com/2013_05_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Friday, May 10, 2013. Some of this is a bit of a repeat for those of you on my Facebook, but I need to do a proper update here :). And had a look at the bikes there. I ended up getting him a regular bike with training wheels to try. I thought that it might be better because the location of the pedals is different and may be easier than the tricycles. In other small news, Joshua finally had a m...
Joshua's Story: February 2015
http://amazingjoshua.blogspot.com/2015_02_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Saturday, February 21, 2015. At the end of January, Joshua started school for the first time. He is in 'Transition', which is the equivalent of Kindergarten in other states/countries. It was an emotional day to send my little man off to school for the first time, but he has been going for 4 weeks now, and I am really happy with how things are going. When he was getting upset at meal times, the...
Joshua's Story: May 2014
http://amazingjoshua.blogspot.com/2014_05_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Thursday, May 22, 2014. Wow 4 years old. There is something about being 4 that sounds really KID like. You can still pass a 3 year old off as a toddler, but 4. it is something else! He definitely isn't a baby anymore. It is hard to believe I have a 4 year old. Because whoa, that sure went fast, but also because in many ways, I really don't have a 4 year old. I'm well aware that my 22 month old...
Joshua's Story: February 2013
http://amazingjoshua.blogspot.com/2013_02_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Tuesday, February 26, 2013. 3rd Appointment with Visiting Paediatric Rehab. Today we once again attended the Visiting Paediatric Rehabilitation Clinic for Children with Cerebral Palsy. This team visits from the Women's and Children's Hospital in Adelaide and comprises of a Doctor, Occupational Therapist, Physiotherapist, some other lady that takes notes (hah! The Doctor noted his presentation ...
Joshua's Story: March 2015
http://amazingjoshua.blogspot.com/2015_03_01_archive.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Sunday, March 8, 2015. The Process of Letting Go. They said it was impossible to know, and that we would just have to wait and see how he developed. I told myself that Joshua was going to be fine. Of course he would be one of those children who beat the odds and go on to have no problems. Of course. At this same appointment, Joshua's head circumference was on the 5th percentile, and I was agai...
Joshua's Story: And the Roller Coaster begins...
http://amazingjoshua.blogspot.com/2010/11/and-roller-coaster-begins.html
Sharing the roller coaster ride after our son was diagnosed with Hypoxic-Ischaemic Encephalopathy (HIE) Grade 2. Sunday, November 21, 2010. And the Roller Coaster begins. So I had gone to get settled in my room on the maternity ward, and Rod had gone home. The hospital midwife came in and told me that Josie had already called to see how I was doing (she had left while I was in the nursery with Joshua.) I was busy texting friends and family letting them know the good news that our boy was here! There are ...
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Noah's Ark Potbellied Pig Sanctuary
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Noah's Ark
Our Journey: Knowing, Loving, Losing and Remembering Noah. Friday, May 3, 2013. Being that today is Starlight Day I thought I'd share our experience and encourage people to give a little. Starlight help to brighten the lives of seriously sick kids and their families, at a time when illness, hospitals and intensely difficult situations have become the norm. It gave us something to plan and look forward to. Something about the future we could smile about. Our trip was booked for the end of October. Well it...
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Dialing In On Selecting a VoIP Service Provider. The VoIP service providers. Inspection and repair plans are generally started around the 20 dollar mark and continue upwards depending upon the customer’s needs and the plans a service provider has to provide. VoIP service providers are asked to provide 911 assistance of any character.The supreme problem with the 911, the VoIP service that is most providers still have still not completely figured out this issue.The name and also the address of 911 ...New t...
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