Friday, July 6, 2018

Flashback Friday


Flashback Friday!

In honor of Flashback Friday AND Airway Disorder Awareness Day (July 10th).

Jaxson at one month old (left) having trouble breathing, eating, and gaining.

Jaxson at sixteen months old (right) eating anything and everything. Can drink 5 to 8 oz of milk in less than five minutes.. AND BREATHING EASY.

Please support Jaxson and his fellow Laryngomalacia Warriors with painting your nails light blue for Airway Disorder Awareness day on July 10th, 2018.


Show your support by tagging/sharing with us on Facebook or Instagram! Tag your photos with #AirwayDisorderDay2018 #LightBlueforLM

Thank you from Jaxson's Mom Jennie

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Sunday, July 1, 2018

Things Not to Say to a Special Needs Parent


Things NOT to Say to a Special Needs Parent....
DISCLAIMER: I am NOT writing this to offend anyone. I AM writing this to show awareness and to be mindful of what we say to Special Needs parents. I asked around a Facebook page today and asked what phrases or words people (friends, family, and strangers) have said that upset them... 
When we were at the Naval Hospital in the very beginning, Jaxson was about three months old and this older lady strikes up a conversation with me. I know she meant well but when she asked how old he was and I replied with: "Three months old," she gave me this look. She thought he was ONE month old, not THREE months old. I know she didn't KNOW that our baby wasn't thriving but it made me feel upset nonetheless. At three months old he was barely a little over his birth weight of 6 lbs 10 oz.

When I tell new people about Jaxson's Rare Chromosome disorder I get a lot of crickets or blank stares. It's not intentional, I know that, it's hard to comprehend--I'm even having a hard time learning about it myself. JUST SO MUCH INFORMATION! I love that I have been able to find a special tribe that understands this journey of ours along with the outpouring of love and support from our friends and families.

"He'll get better or he will outgrow it.."
Unfortunately with certain Rare Genetic disorders is that they aren't going to get better like someone would from an illness or outgrow it like a child outgrows training wheels. Our warriors just learn to LIVE and ADAPT to their disabilities. Jaxson surprises us every single day with his accomplishments!

"Your child doesn't look sick or he doesn't look autistic.."
I know it's meant to be nice but in all honesty, it really isn't. When someone tells you about their child and about their Special Needs or Rare Genetic Disorder, please don't tell them they do not look sick, they look normal, or happy. A Special Needs child and a child with a Rare Genetic disorder do not fit a specific "mold" or "one size fits all" so to speak. Two children can have the same genetic disorder but exhibit different symptoms and features.

"How old is he? ...Really he is?"
Like most of the children with Special Needs or Rare Genetic disorder, Jaxson is developmentally delayed and speech delayed. His physical therapist stated that he is at about 8/9 months delayed so that would put him at about a 8/9 month old child level based on that diagnosis. So yes, he acts and appears to be younger then he is but he is 16 months old. I know this is unintentional like the Naval Hospital incident but it still makes me and others upset when are children are compared to others their age.

"Have you tried changing their diet..?"
Yes. Yes we have. Jaxson has mild dysphagia which makes it difficult to swallow, he has come a long way with Feeding Therapy but it still lingers. Because of his Rare Genetic disorder, we aren't sure if it's going to be a temporary thing or if it's going to be long-term. Children with G tubes, NG tubes, etc. They're on there for many different reasons, and asking them if changing their diet or have you tried changing your child's diet isn't something they want to hear. Like most, they've exhausted every possible avenue prior to having their children undergo life saving surgery for a feeding tube.

"He/She doesn't act like so and so's child.."
I haven't dealt with this personally but a couple of moms on the Facebook page have and nothing is more disheartening or upsetting to hear that your child is anything but "normal." Please don't compare Special Needs children to other children.

I know I am super POST HAPPY the last couple days. I just really enjoy writing for this blog.. it feels very therapeutic.. like I'm finally lifting all this stress off of my shoulders. I hope I will be able to help someone else who is struggling for answers.

Want to share your experiences with me? Please leave a comment or message me, I would love to hear from you.



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Saturday, June 30, 2018

21 Facts About Mom


Wanted to give our readers some facts about mom!
  1. I am half Okinawan and a mix of Irish, Swedish, Welsh, German, and French Canadian.
  2. I can speak fluent Japanese.
  3. I love to bake.
  4. I took ten years of karate and I am a third degree black belt.
  5. I have two tuxedo cats: Oreo and Voltron.
  6. I love Romance novels.
  7. I hate my freckles.
  8. I was an Air Force brat.
  9. I love horror movies.
  10. I'm very self-conscious AND super awkward.
  11. I'm currently taking classes towards a degree in Medical Billing and Coding BUT I do have a B.S. in Health Care Administration.
  12. I love Olympic Weightlifting/Powerlifting.
  13. I LOVE FOOD.
  14. Buffy the Vampire Slayer is my jam.
  15. Knew my husband THREE months before we married--celebrated NINE years this past April.
  16. I hate cardio.
  17. I have an addiction to donuts.
  18. I hate the summer--specifically the humidity.
  19. I have ten tattoos.
  20. I have an unhealthy obsession with leggings/yoga pants.
  21. I am an active duty USMC spouse.
Thank you for taking the time to read about Jaxson and his family!


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Wednesday, June 20, 2018

Warrior Wednesday

Today is Warrior Wednesday, and where do I even begin?


For Warrior Wednesday, they ask you to recognize someone who went above and beyond for your family. The only problem is that not just ONE helped us through this journey.

When I was at the Children's Hospital for a week, unable to leave Jaxson I had amazing friends who stopped by with coffee, snacks, watched Jaxson while I slept, kept me company, and JUST being there. You all are the real M.V.P. Thank you Jean R., Ashley P., and Naomi M. You all are truly amazing, thank you! Thank you for helping us with the boys and keeping an eye on them when we had to go to appointments, date night, or just needed a little break.



My dear friend Michelle R., you are truly a great friend. You came running to help when James and I were both down with whatever the heck that was--we couldn't eat or drink without throwing up--and couldn't even care for Jaxson who was sick as well. You also stopped by when we were in at the Children's Hospital to allow me to go down to get breakfast or coffee. Listened to me vent or cry when I needed it. YOU'VE DONE ANYTHING OR EVERYTHING! Thank you so much.

Lynne B., I'm so glad we met. You have no idea how thankful I am you were there when I got that phone call from our UAB team. I really appreciated you coming over a couple weeks ago to hang out and make some Okinawan Donuts lol. It wasn't much but it was fun! Thank you for everything, thank you listening, just thank you!

Our family The Carforas, going out of their way to help me go to University of Birmingham for Jaxson's Genetics or Aero Digestive appointments, taking us away for a weekend, listening and answering all of our questions--I love you all so much, thank you. Mom and Dad, thank you for raising me to be strong, I love you both so much.



My husband, you are truly a warrior too. You are an amazing husband and father and thank you for all of the sacrifices to support our family. I know it is difficult being away from your family but you do it to ensure that we have everything we need. I love you so much!!!!

Lastly, Jaxson's Pediatrician. Dr. Southwick went out of his way to ensure that we were seeing all of the right specialists, listened, and was and still is very thorough. I'm thankful to have you as my child's doctor and we will miss you when we PCS in the fall.

Thank you all from the bottom of our hearts.






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Tuesday, June 19, 2018

Telling Tuesday

June 17th - 23rd is Rare Chromosome Awareness Week and I wanted to participate in it as well. As you know from my first post Jaxson has been diagnosed with a rare genetic condition they call DYRK1A Deletion Syndrome.

Jaxson watching Baby Signing Time
What is DYRK1A exactly?

DYRK1A is a gene that is involved in brain growth. It was identified several years ago but only recognized to be associated with a neurodevelopmental condition in 2008. The DYRK1A gene is on chromosome 21q22.13 and is one of the genes that is missing in the 21q22.13 deletion syndrome. When we compare children with the 21q22.13 microdeletion syndrome and those with changes in the DYRK1A gene, many of their features are similar. We now think that the key features of 21q22.13 microdeletion syndrome are caused by absence of DYRK1A (RareChromo, 2015).

Other names for DYRK1A:

  • Dual specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
  • DYRK
  • MNBH

Features Associated with DYRK1A:

  • Autism Spectrum Disorder (ASD)
  • Epilepsy/Seizure Disorder
  • Intellectual Disability/Developmental Delay
  • Small head/Jaw
  • Difference in Facial Feature
  • Small size during Pregnancy
  • Abnormal gait
  • Hypertonia
  • Failure to Thrive/Feeding difficulties

Other Symptoms:

  • Gastrointestinal 
  • Cardiac
  • Skeletal
  • Genitourinary

Cases of DYRK1A:

  • To date there are 188 families on our support page with loved ones who have the DYRK1A deletion syndrome.

Rare Disease Statistics 2018:

  • In America, a rare disease is when it affects less than 200,000 people. 
  • Signs and symptoms of rare diseases can differ in each individual who has the condition.
  • On average it takes FIVE years for a rare disease to be correctly diagnosed.
The day we got the diagnosis April 25, 2018


References:

DYRK1A and 21q22.13 Deletion. (2015). Retrieved from https://www.rarechromo.org/


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