Rayden's orthodist, Bob, placed these carbon fiber rods on the back of his AFO's to prevent him from leaning forward. If you look closely at the picture you can see where his AFO's are bent and almost broken because he is leaning forward so much. This is a temporary fix until he gets his replacement pair that will have more support and then ultimately a new kind all together.
Welcome to Rayden's page. Here you will find a story of our sons journey with Spina Bifida. There have been many challenges and struggles through the years but it's been worth it! I have tried to keep this blog updated. It might be easier to navigate by using the side bar and looking for specific dates or posts. You can even use the search engine for something specific. I welcome comments as well.
Sunday, July 19, 2020
July 12, 2020 "First boat ride"
Rayden has always been fascinated with boats. His favorite store is Cabelas because he can get in every single boat and pretend to drive it around. Gerome Heath (Uncle G) got Rayden a life jacket when he turned 4 years old in hopes to take him for a ride on his boat. That year was filled with surgeries, casts, homebound, and intense therapy. It is finally safe to take him on a boat ride and Rayden could not be happier! Watching how much he enjoyed his time on the boat was absolutely priceless. His body was overflowing with excitement. His eyes filled with joy. His laughter was contagious as his smile stretched from ear to ear. He kept screaming, "This is sooo much fun!" and "It's as fast as a jet engine!"
| Second boat ride! |
Saturday, June 6, 2020
May 31, 2020 "Corona virus quarantine=Home schooling"
Thursday, June 4, 2020
May 26, 2020 "Most HELPFUL kid ever!"
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| Holding flashlight, painting camper, installing water line and TP holder. |
Rayden is the hardest working kid I've ever seen in my life. No exaggeration!! He literally is obsessed with working. He enjoys helping Daddy more than anything else in this world. He's actually pretty gifted when it comes to tools. He can identify most by their correct names and uses them properly as well. The 'work truck' he got for Christmas has really come in handy. Rayden loves to haul things for us (boxes to the burn pile, groceries, grass clippings, packages, anything!) The first thing out of his mouth every morning is "What are we going to do today?"
| Supervising electricians, putting together the fridge, converting the stove to LP. |
| Digging gas line, pulling up stumps, hauling cleaning supplies, installing dryer. |
| Cleaning his shower, putting his bed together, delivering groceries, installing Daddy's shelves. |
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| Vacuuming closet out. |
| Putting the back on mom's cabinet, hauling grass, cooking, pulling up stumps. |
Thursday, April 16, 2020
April 12, 2020 "Easter"
This Easter sure is different than any other in our life. Corona Virus (Covid 19) has had us quarantine since March 16 with no real end in sight. The good thing though, is that we were able to move back into our house April 4 after living in a camper in the backyard for six months. The remodel is AMAZING and I'm very thankful for this time off work to move back in. Rayden wanted to have a 'sleep over' in the living room the night before Easter. So we blew up the air mattress and watched Toy Story 4. Of course, Rayden was asleep within an hour. When he woke up the next morning he was delighted to find his Easter basket full of goodies. Yes, I allowed him to eat some chocolate before breakfast! We even had a little egg hunt in the back yard. Rayden enjoyed hiding the eggs for Mommy to find. He thought it was super funny when I couldn't find them all. It is amazing to see Rayden in the videos walking all over the yard WITHOUT his walker. He is getting so independent.
Thursday, March 19, 2020
March 19, 2020 "Dressing up for school"
Rayden enjoys dressing up. When he got the chance to do it for school it was even more special. The only problem is he expected to dress up every day!
Friday, March 6, 2020
March 6, 2020 "Opthalmologist Appointment"
Rayden had not seen Dr. Grace since this past summer. I could really tell a huge difference in him from his last visit. He would not cooperate or tell them anything the last time we came. Dr. Grace couldn't even examine him really. This time he was amazing. I didn't have to hold him down or even have him sit in my lap. He covered his eyes accordingly and told each exam assistant everything they needed to know. He sat perfectly still for Dr. Grace to examine his eyes. She said his optic nerves are still swollen (permanent damage, so not surprising). His prescription is 20/60 right eye and 20/80 left eye. With this vision he would need to continue wearing his glasses to read/write. She seemed more concerned with his left eye. Although Rayden had strabismus surgery on his eyes and we have been patching four hours a day, it is STILL drifting inward. She believes his left eye should be doing as well (responding to treatment) as his right eye but it isn't. When she had his right eye covered she showed him a picture but he said he couldn't see it. She asked him numerous times and he tried hard but couldn't. When she gave up and uncovered his right eye, he said "Oh, it's a Christmas tree." He can clearly see much better with his right eye. She believes this is also the root of his fine motor problems. Due to this lack of improvement she is referring him to Dr. El-Dairi, Pediatric Neuro-opthalmologist, to get better optic nerve pictures at the main Duke office. Her theory is the prolonged high intracranial pressure on his optic nerves before birth has caused more permanent damage to his left side and there really isn't anything she can do to correct it. Here again, Rayden writes his own book. He is just so unique. I'm very thankful to have such wonderful doctors that work so well together and have genuine concern for his well being. I don't know what the future holds for Rayden with his vision, but I know God has a plan.
Friday, February 21, 2020
February 20-21, 2020 "Blippi concert and snow"
Rayden was super excited the entire concert continuously saying "Look Daddy!" Priceless! Of course, by the time we exited the concert the van was covered in snow! It was a long, slow, scary drive home but we made it a wonderful memory for Rayden and I am so happy he was able to experience it.

SNOW- Rayden was still overly excited when he woke up because there was snow all over the ground. It wasn't a lot (just enough to make a kid happy). I got him all dressed up in his snow pants, coat, furry hat, gloves, and boots. He enjoyed singing "Walking in the snow" and throwing snowballs at Mommy.
Friday, February 14, 2020
February 14, 2020 "New AFO's fitting"
Sunday, February 2, 2020
January 30, 2020 "Surgery #14-Removal of hardware in hips/femurs"
gave out quick kisses and hugs to Nanny, Papa and Granny before we entered the Pre-Op area. I suppose UNC is just so familiar to Rayden because he seemed alright with the whole thing until we got back there in a room. He started asking why we were there and refused to sit in the examining chair or take off his clothes. After the nurse, anesthesiologist, interns, and nurses all did their rounds they gave him the versed to make him sleepy but it didn't seem to work as well as last time. He was way too aware of what was going on.
| Plates and screws in Rayden |
| Lite-Brite |
A real interesting note: Rayden began telling us about his surgery experience this weekend. Apparently he remembers the wagon ride. He told us the people with the masks took him out of the wagon and laid him on the bed. He said they were talking to him and he didn't cry either. I asked him if they put the gas mask on him but he said no. I guess that's all he remembers. We explained the surgery to him. He seemed to understand asking if they used a "drill and scalpel." He's such a smart, strong, brave, sweet little boy.
Monday, January 6, 2020
January 6, 2020 "Pressure Sore"
Wednesday, December 25, 2019
Saturday, December 14, 2019
December 14, 2019 "Shriner's Christmas Party"
All the clowns escorted Rayden outside to the parade bus. The music was blarring and Rayden immediately transformed into a real clown! His adorable dancing melted every heart in the parking lot! They even allowed Rayden to climb aboard the bus (only REAL clowns can do that!) We enjoyed a nice meal, games, cake walk, crafts, and of course, Santa. I hope these wonderful clowns know how much they mean to Rayden and just how much they made him smile. He talked about becoming a clown to everyone he saw for weeks after and continuously asks to watch the video on my phone. PRICELESS!!!

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