Logan's Story: On to his next journey

Saturday, May 27, 2017

On to his next journey

Our dear Logan Michael passed away peacefully this morning May 27th at 12:20am. Joel, Lauren, myself and his grandparents were here to see him off on his next journey to heaven. Logan has left his mark on this world and will now be with loved ones awaiting him in heaven. He is now free and we are comforted knowing he will no longer be in pain. Our Bubba will be sorely missed but we know he is smiling down on us!!

2 comments:

CSIAmandaMay 27, 2017 at 4:13 PM
My heart goes out to all of you . Logan truly touched my heart all the way here in Ottawa, Ontario, Canada.
His strength and yours as a family always wowed me an gave me strength to face things. My thoughts are with you.
Fly Free Logan
ReplyDelete
Replies
UnknownFebruary 10, 2018 at 12:02 AM
A fine, fitting farewell to an iconic character, LOGAN is one of the best superhero movies ever made.

Logan full movie online free

Watch Black Panther putlockers
ReplyDelete
Replies

Add comment

About Logan

This blog is a story of Logan. He is our six year old son who is developmentally delayed with a diagnosis of a neuro degenerative disorder. He has degeneration of the basal ganglia (part of the brain) and many types of seizures on a daily basis. His seizure type is Lennox-Gastuat. We have done exome sequencing and mitochondrial testing among many other paths of testing but have yet to find an official diagnosis. His other known problems/diagnoses include problems with swallowing (aspiration), hypotonia, cortical visual impairment, and degeneration in the macula of the eye.

Logan was born without complications but began to have feeding difficulties right away. He never took to breast feeding and when he drank a bottle he would vomit copious amounts of formula. He has problems with abnormal movements of his arms and legs, spasms of the legs, and inability to hold his head up for lengths of time or sit on his own.

Logan is nonverbal and is at the developmental age of 4-6 months. He is unable to take food or drink by mouth due to aspiration difficulties therefore he has a feeding tube. He has a tracheostomy to aid in clearance of secretions and had the removal of a few of his saliva glands.

We hope this blog will allow our family and friends to follow along in his journey and possibly bring ourselves into contact with other families dealing with the same day to day challenges.

~Joel, Rachel, Lauren, and of course... Logan