Heni Marie Biesinger - Miss

Heni was our second child out of four and was born with a genetic abnormality called Edwards syndrome (full T18). We expected her life to be short but were blessed to have her in our lives for 21 years with many ups and downs and health issues along the way. When she was alive we started documenting her story online and continued after her death. If you wold like to know more about her and our story you can find some of it at the links below. By doing this Turning Hearts medallion we hope that all who come across Heni's bench at Pullwood Bay may get to know a little bit about our beautiful daughter. For such a small person she had a huge impact on our lives. She was pure unconditional love and spread joy to all who met her and we sorely miss her presence.

Heni's story part 1 http://henibean.blogspot.com/2015/04/
Heni's story part 2 http://henibean.blogspot.com/2015/05/henis-story-part-2.html
Heni's story part 3 http://henibean.blogspot.com/2015/07/heni-story-part-3.html
Heni's story part 4 http://henibean.blogspot.com/2016/02/henis-story-part-4.html
Heni's 21st http://henibean.blogspot.com/2016/07/21-today.html

We hope the photos, videos and blog links bring a smile to your eyes, joy to your heart and hope for the future.... and that your come to know Heni just a little bit and understand the immense loss that it is to lose someone so precious. Hold on to those you love. Tell them you love them and make the most of this one short life.

with love
The Biesinger Family.

If you would also like to honour your deceased loved one and gain a turning hearts medallion so that you can share their lives with others, you can obtain a medallion by clicking on the link below.
https://turninghearts.com?sca_ref=5257224.I0sd6xR0w7