By definition, #laryngomalacia is a common, benign disorder of the airway. Most babies will continue to grow, meet milestones and will not need any further medical intervention after the initial diagnosis.
However, 5% of babies are diagnosed with life threatening LM and require surgery, generally- emergency airway surgery.
Coping With Laryngomalacia, Inc.'s fundraiser, '#luthelamb Is My BFF' ends in just ten hours.
The support has been overwhelming and I thank everyone who has already given.
Perhaps, you haven't seen my posts on social media. You don't normally check your Email-so you missed it there, too. Or since you do not have a baby with life threatening LM- you don't believe in the cause. There is no reason to, right?
I am asking you tonight to pause. Just for one moment.
What would you do if you were told your newborn needs emergency airway surgery-for an airway disorder that is supposed to be benign?
What would you do? Who would you turn to?
What would you say as you placed your baby in the arms of a surgeon?
Where would you find strength as you sat in PICU and watched your baby breathe with a tube down her throat?
HOW WOULD YOU COPE?
With your donation of just $20, you will receive a Limited Edition CWL shirt and one care package will be sent to a baby in PICU recovering from airway surgery.
Your support is needed and appreciated.
Please do not hesitate and give now. Link in bio. 💙
CWL Founder & President
CopingWithLM.org #copingwithlm #fundraiser #lightblueforlm #nonprofit