This is an amazing group that has given us so much more information than we have ever received from any medical professional. Our ENT is wonderful but we found him after reading the stories of other LM families and deciding that we needed to speak up at the pediatrician's
Mission: to provide support, strength and education for families coping with LM, TM and BM.
Located in Port Monmouth, New Jersey (USA)...serving families worldwide.
Results: Thanks to our amazing donors, we have sent close to 500 care packages all through out the USA, Canada, The United Kingdom, South Africa, Australia and The Netherlands!
Target demographics: families worldwide
Direct beneficiaries per year: over 1,000 families
Geographic areas served: Port Monmouth, New Jersey
Programs: 24/7 online support
Live online chats
Breathe Easy Care Package Program
Pint-Sized Powerhouse Grant Program
Malacia MeetUps
CPR training
Breast, bottle & tube feeding support
Tracheotomy tube education and support
Awareness apparel and merchandise
Education resources and more!
This is an amazing group that has given us so much more information than we have ever received from any medical professional. Our ENT is wonderful but we found him after reading the stories of other LM families and deciding that we needed to speak up at the pediatrician's office. We are grateful for the support shown to us through their wonderful facebook page as well as a very kind care package we received before a surgery. This is a nonprofit that truely supports it's cause.
Very supportive to new parents. My daughter was diagnosed at birth after her father and I insisted that something was wrong. We both were familiar with newborn cries and here just wasn't right. We also noticed she breathed weird. She has a tracheal tug and GERD as well (which we noticed in the hospital right after birth). She was finally put on reflux meds this week. She's been on breathing treatments since she was 4 months old. I've found so much support and comfort in this group!
