WOW  we just celebrated kayden's 12th BIRTHDAY June 19th!!! That feels so good to say and makes me smile so big while thanking the Lord for so many amazing times together. I pray for may many more to come.
Im so excised to say that Kayden is doing amazing this last year!!! We started him on a probiotic called Bio-Kult and it is some amazing stuff  that has helped keep kayden healthy. He only got sick like twice this winter and was so mild. Many of us in the family were very sick and kayden did not catch it. I recommend this natural and wonderful probiotic to everyone. you can read about it here http://www.amazon.com/Bio-Kult-F7057-B-Probiotic/dp/B004XKUD78/ref=sr_1_1?ie=UTF8&qid=1375829336&sr=8-1&keywords=bio-kult Please keep him in prayer to continue to do so well. We also started blending most of kaydens food now and have seen less constipation since starting him on real food as well as organic extra virgin coconut oil which has some amazing benefits its self.

Kayden has however been having reoccurring smelly ear and blood drainage in his left ear. This is the ear that 7 years ago he had a cholesteatoma "tumor" removed from. Because he has had some of the same signs he is having today  he will be going in for exploratory surgery at the end of the month on this ear to see if he has another one. please keep Kayden is your prayers and that everything will be just fine.   http://en.wikipedia.org/wiki/Cholesteatoma

This last march we got to celebrate the lives of so many trisomy kids at our annul trisomy families conference which was held this year here in MN. This next March we can not wait to see everyone in AZ. Late April Kayden and my self were also fortunate to take a little flight to AZ to celebrate a little boy named Santi with trisomy 13 and spent a week with him and his family. we are so happy to be apart of so many other families life touched by trisomy.

I have been very busy with my advocating and co-founding Trisomy Families.We are in the middle of trying to pull our website together http://trisomyfamilies.org/ but for now have a amazing HUGE facebook support page for so many families faced with loved ones touched by trisomy. If you or anyone you know is touched by any trisomy please find us here. https://www.facebook.com/groups/trisomyfamilies/

Kayden now has a facebook page please find him and "like" his page!!! https://www.facebook.com/KaydenTheHopeInTrisomy18

Also Trisomy Families has started our own magazine and you can order any issues here.http://www.magcloud.com/user/juliehowerton