Prayers for Ambrose

Kyle and Bridget have been to numerous doctors and physical therapy appointments for over a year trying to figure out what is going on with their 2 year old, Ambrose - he developed a difficulty swallowing as well as an inability to walk. Eventually, this led them to a genetic panel test. He was diagnosed just before Christmas with a rare genetic disorder called Metachromatic Leukodystrophy. It is progressive and life-threatening. Ambrose's parents are both recessive carriers of this gene mutation; each of their children have a 25% chance of inheriting this condition. His family is still in search of somewhere that will treat him. Without treatment, Ambrose will lose many of his senses and abilities that are easily taken for granted... Due to him showing symptoms of this condition, they are told that he is not eligible for treatment. Without treatment, his life expectancy is 6-7 years. They all need a miracle. Please pray that none of their other children have MLD.

Please help their family in their search for a treatment and to help with palliative care. This will be costly for their family and will require many days away from work to keep him comfortable and hopefully find treatments that will work to heal him. Thank you for your consideration and donations in this trying time.

As Kyle and Bridget always say, "Everyone has a cross." Please pray for their family to lighten their cross.

There is also a benefit fund set up:

Ambrose Roth Benefit

Sterling Bank

234 East LaSalle Ave

P.O. Box 70

Barron WI 54812

715-537-3141