Photographer, Educator, Student, Mother & Wife Obsessed with sharing moments through pictures & words
“You never know how strong you are until being strong is the only choice you have.” ~anonymous Times have been busy and I’m anxious to share a lot of new work in the week ahead. With it being spina bifida awareness month, I prolonged sharing my favorite photos from Yadiel’s session so that you all […]
Unfortunately, it’s not just in other cultures. There were still some parts of the US that were pniushg for nontreatment when I was born. (I’m only 25.) In fact, when I was born, my mother’s doctors were all encouraging her to give me up to the institution because I probably won’t live long anyway. They told my mother, who had been hoping for a baby for 5 years and had just had an emergency C-section to save the precious life within, to just give me up because I wouldn’t amount to anything and would be dead before my 10th birthday anyway. My mom, being the wonderful stubborn woman that she is, told the doctor where to stick it and that she would just have to do the best she could raising me. I’m 25, a college graduate with a driver’s license, a wonderful job, and a loving boyfriend (who will hopefully be a loving fiance9e sometime soon).
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It’s hard to believe it’s been five years since our little guy Jaylen was born. I’ve blinked and now he’s such a big boy…so proud to be five. He’s such a loving, charming, and fun little kid these days. I visited him just before it was time to pick him up from pre-k today and […]
by Amanda Kern
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“She not only saw a light at the end of the tunnel, she became that light for others.” ~ kobi yamada If you mention “D-day” to most the thoughts of troops storming the beaches of Normandy might enter their minds. But if you ask most parents of a child with spina bifida they likely will […]
by Amanda Kern
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such a strong and handsome fella <3
You’re right, D day means something entirely different to some of us. I can not only tell you the date, but all the details of the days Justin was diagnosed with Type one diabetes and then Epilepsy. I will never forget. Both broke my heart.
Chance has to have the sweetest face ever and I am so glad his story has been able to reach others. I’m sure you know how it feels to find someone who understands and those families are blessed that you are willing share your families journey with them.
I look forward to seeing what he can do next year… He is truly an amazing young man.
I just received results for my screening and it came back positive for NTD greater than 1 in 10 chance. I came across your blog and have read every post since I can’t seem to sleep tonight:/ I just want to say thank you from the bottom of my heart for your blog and you sharing every moment. I go to the maternal fetal medicine for a level 2 ultrasound. But I’m going to walk in the office so much more educated and optimistic. Thank you again.
Last week I got to meet with Jacqueline & Jermaine’s family to take their daughter Madison’s newborn photos. A little over three years ago I first met them as I took their son Nathaniel’s photos. I’ve done photos a couple times for their family so the moment I heard the news about Madison I was […]
by Amanda Kern
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If you’ve been following along with my photography on my blog you may recall photos I took this summer of Lindsey’s family just a few weeks before her baby girl arrived. Though I didn’t get to meet with them as soon as we’d have liked to for newborn photos, we got together recently to capture […]
by Amanda Kern
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by Amanda Kern
11 comments