Monarch Global will be joining West Coast Customs and The Whale Tail Project as they share the floor with Porsche at Moneterey Car Week!


Join us on Monday, August 9th for Monterey Car Week as we share the floor at Porsche Moneterey while their team unveils the ultimate Porsche build off! Also unveiling their Porsche 911 is the world famout West Coast Customs! See the reimagined custom 911 brought to you by one of the best automotive customizers in the world. The Whale Tail Project, a designer's dream of the infamous Porsche Turbo Tail, will be on display and available for auction as well!

Your financial support can help us sponser a child with CF

With over 75% of children with CF diagnosed before the age of 2 years old, families are faced with a terrible realization that the odds of their baby living a normal life is highly unlikely. The lifespan of a child with Cystic Fibrosis is typically less than 18 years, however with support, treatment, education and research, Monarch Global is committed to helping these children overcome the challenges and difficulties they face to live longer lives.

Marten Devlieger , AKA CF Adventurer, supports Monarch Global


Public speaker and Cystic Fibrosis fighter, Marten Devlieger, shouts out to Monarch Global in his latest videos. He developed what is now the Monarch Airway Clearance System which is a mobile airway clearance system for people with Cystic Fibrosis. This device has greatly impacted his life and others’ around the world. Through this opportunity he was lucky enough to have the privilege to start public speaking around the world to encourage people to live an active healthy life with Cystic Fibrosis.

 

 

OUR MISSION

 

Monarch Global Foundation is a non profit organization dedicated to helping people all over the world who suffer from Cystic Fibrosis. We are dedicated to helping "find the cure to cystic fibrosis and helping provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized care"

 

Our Work

 

As owners of a Limousine Company and having two children with cystic fibrosis, it became our responsibility to help fight this disease every way possible. One of our goals is to convert our entire fleet to completely ECO friendly green limousines. This will help the environment from less gas pollution to other toxins that may cause people to have allergic reactions.   

 LATEST NEWS 

 Monarch Global will be attending Monterey Car Week!

We'll be hosting an exclusive special event at Monterey Car Week (August 6-13) featuring West Coast Customs and their newest 911 Carrera. Be the first to see the amazing Whale Tail project and have the opportunity to own a piece of history. 

 Monarch Global Partners with West Coast Customs! 

World Famous West Coast Customs is notorious for building some of the most unbelievable custom vehicles in the world.  West Coast Customs and Monarch Global have now partnered to build vehicles that help educate, support and help find a cure for CF.

Marten Devlieger - CF Adventurer

Marten Devlieger is a 39 year old husband and father of 2 children ages 8 and 10. He was born in Zierikzee Holland. After being diagnosed with Cystic Fibrosis, a fatal genetic disease, his parents chose to immigrate to Canada where he resides today, due to hope for a better life with Cystic Fibrosis. Early in his life he became an adventure athlete: windsurfing, kiteboarding, snowmobiling, etc. He became a helicopter pilot at 18 years old and flew commercially for several years until hisCystic Fibrosis and CF liver disease got worse and the government took his license away. At that point he had to decide what direction in life he wanted to go. This led him to develop what is now the Monarch Airway Clearance System which is a mobile airway clearance system for people with Cystic Fibrosis which has greatly impacted his life and others’ around the world. Through this opportunity he was lucky enough to have the privilege to start public speaking around the world to encourage people to live an active healthy life with Cystic Fibrosis.

With nearly 30,000 cases here in the US alone and over 1,000 children born with this disease each year, our mission is to help create the best quality of life and experiences for these children while educating others and striving to help find a cure.