Madison's Story


Images Captured by D4 Photography

Meet Tiny Light Madison, a two year old girl with an inspiring smile and a love for singing and dancing.  She loves to spend her time playing with her pet bunny, learning new words, reading with Mommy and Daddy and playing at the park. 
At only nine days of age, Madison was diagnosed with Congenital Adrenal Hyperplasia (also known as CAH or 21-Hydroxylase Deficiency).  People with CAH are missing an enzyme the adrenal glands use to make cortisol and aldosterone.  Both of these hormones are very important for survival. Cortisol is produced in times of stress; without it, people go into shock very easily.  This is referred to as an Adrenal Crisis.  This condition can be managed but becomes a problem in times of sickness and injury because our bodies would normally produce extra amounts of these hormones. 
Madison’s parents were terrified upon hearing the diagnosis.  They had never heard of CAH, and it all seemed so overwhelming.  “The thought of having to keep up with these medications and not messing them up was so scary. We were scared to tell anybody, we thought nobody would understand.  We were also scared about our daughter's future.”  However, Madison has responded very well to her daily treatments and is thriving.  But as the parents explain, “the hardest part has been the constant fear of Madison getting sick or hurt and having an Adrenal Crisis.  Although she has not had one yet, it is inevitable that one day she will and we always need to be prepared for it.”
The future looks bright for this Tiny Light, as she should be able to lead a healthy, happy life with the help of medication and careful treatment of illness and injury.  As long as she is careful, Madison will be able to accomplish whatever she puts her mind to.  Her parents dream of Madison growing into a very happy, well-rounded person, who goes for what she wants in life.


Story written by Amber Grant






















Kamryn's Story

Images Captured By D4 Photography

This sweet Tiny Light is Kamryn.  She is an inspiration to so many people around her, both those who know her and those who do not, because of her strong spirit and determination to not let anything stop her from doing the things she wants to do.



Kamryn was originally hospitalized for RSV and acute bronchiolitis.  However, during the course of her illness, she contracted Group A Strep and Bacterial Pneumonia.  She was flown to another hospital and she was placed on life support because she was in Septic Shock.  The wait to find out if she would live was agonizing for her parents.  When she finally stabilized, Kamryn showed a zest for life and a happiness that has been amazing!



After her battle with severe infections, Kamryn does not look the same as other children.  She has a total of two and a half fingers.  She has lost part of both her legs including a significant amount on her right side.  However, these things do not get Kamryn down. She can pick up things, hold her own bottle, and even crawl around.  She loves to dance, play with dolls, and keep up with her brothers.



Kamryn’s parents feel that it is important to stay positive and keep looking forward rather than spending time wallowing in what might have been.  Their goals are to encourage Kamryn in everything she desires as she grows.  They want her to do all the things that other kids do.  They want her to continue to be the strong, inspiring, and beautiful light that she already is in this world as she conquers all of the challenges that come her way!


Story by Shauna Salmon