Monday, October 1, 2007

Intro Post

Jake Sidney Reiss and Luke Rae Reiss were born on May 27th, 2007. Within minutes of their birth in the delivery room, we realized something was different about Jake, something that we would soon find out would change his path and our lives forever. Jake was diagnosed with Apert syndrome which is a rare genetic mutation in approx. 1 in 200,000 births that when it occurs causes fusion of the hands and feet as well as premature fusion of the sutures in the skull. Due to this condition, Jake will face many surgeries to alleviate the many characteristics of this disorder.

Apert syndrome is primarily characterized by specific malformations of the skull, midface, hands, and feet. The skull is prematurely fused and unable to grow normally; the midface (that area of the face from the middle of the eye socket to the upper jaw) appears retruded or sunken; and the fingers and toes are fused together in varying degrees.

Children with this disorder are affected in other ways besides the physical characteristics that are common across the syndrome. Some have normal intelligence while the majority are a little slow with an IQ around 100, and then a small minority have more extreme mental challenges.

Jake so far has impressed the many doctors that have met with him and they are encouraged by what they see. Other families with Apert children have also commented on Jake having a seemingly mild case. We are encouraged and so far he has been on par with developmental milestones. We can only hope as one Dr. mentioned, that Jake will be in the upper echelon for this disorder.

We plan on using this as an effective way for family and loved ones to keep up to date with Jake's recovery from his many surgeries and his general progress. We encourage all to visit the blog for updates especially during his surgeries so we can update everyone without having to retell his story over and over again.

Jake's first surgery will take place in Boston by the world renowned surgeon Joseph Upton. Upon meeting Jake, Dr. Upton fulfilled our first dream by informing us he could give Jake five fingers on each hand and make this happen in only two surgeries. Previously, we were told he would only have four fingers and it would require 10 surgeries.

We are committed to giving Jake the best medical care he can receive and as you can see already we are willing to travel if it means the best doctors will work on Jake.

Lastly, we welcome you to Jake's blog and we know the journey ahead will be long and challenging but we invite you to share in the experience and propel Jake to great heights through all of our collective positive thinking.

7 comments:

iweinrot said...

Dear Sam & Lance,
Thank you for updating us on your journey. Jake is certainly lucky to have such devoted & loving parents.
We wish you all the most positive outcome on Jake's pending surgery.
Love,
Irene & Allison

Samantha said...

We will be along on the journey. Those photos are so adorable. You've been blessed with two really wonderful boys. And they two wonderful parents.

Love, Lisa, Richard and Samantha

susan said...
This comment has been removed by the author.
susan said...

The blog is awesome! The pictures of the boys convey the friendship and bonding that they have formed. Thanks for including us on your journey. We will be keeping Jake in our hearts and prayers as we wish you success on his upcoming surgery.
Love, Susan and Lenny

Unknown said...

Sam and Lance,
This blog is great and the photos are adorable. Your boys are really cute. We will be thinking of you on November 7th and send you all our love. Our prayers are with Jake and we will follow his journey on the blog and through Stacey. xo
Justine Stamen Arrillaga

Anonymous said...

Thanks for directing me to the blog tonight. We always have you four in our prayers.

Good luck in Boston next week.


Eric, Joanna and Tilly

Anonymous said...

Lance, that is a fantastic outcome for the little man. Louisa is thinking about him and Lukey and hopes to see them home soon. We look forward to seeing you next week.