My BWS Baby
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  • Beckwith Wiedemann Syndrome BWS Genetics, AFP, and Scans BWS Resources Tongue Reduction Information Life in the NICU
  • Jacob's Birth Story Tongue Reduction Surgery Feeding Issues The First Year A Day in the Life of BWS BWS & Beyond (The Later Years)
  • Nutrition
  • BWS Buddies
  • BWS Bracelets BWS Awareness Shop BWS baby products
  • Donate
My BWS Baby
  • About/
    • Home
  • BWS Support/
    • Beckwith Wiedemann Syndrome
    • BWS Genetics, AFP, and Scans
    • BWS Resources
    • Tongue Reduction Information
    • Life in the NICU
  • Jacob's Journey/
    • Jacob's Birth Story
    • Tongue Reduction Surgery
    • Feeding Issues
    • The First Year
    • A Day in the Life of BWS
    • BWS & Beyond (The Later Years)
  • Nutrition/
  • BWS Buddies/
  • Products/
    • BWS Bracelets
    • BWS Awareness Shop
    • BWS baby products
  • Donate/
Butterfly poem.jpg
My BWS Baby

Discovering life beyond the diagnosis. Beckwith-Wiedemann Syndrome

BWS Buddies

Our BWS Buddies. Share your story about Beckwith-Wiedemann Syndrome and read a collection of stories from others to help you through your journey. #BWS #BeckwithWiedemannSyndrome #HowBigBWS

My BWS Baby
  • About/
    • Home
  • BWS Support/
    • Beckwith Wiedemann Syndrome
    • BWS Genetics, AFP, and Scans
    • BWS Resources
    • Tongue Reduction Information
    • Life in the NICU
  • Jacob's Journey/
    • Jacob's Birth Story
    • Tongue Reduction Surgery
    • Feeding Issues
    • The First Year
    • A Day in the Life of BWS
    • BWS & Beyond (The Later Years)
  • Nutrition/
  • BWS Buddies/
  • Products/
    • BWS Bracelets
    • BWS Awareness Shop
    • BWS baby products
  • Donate/
April 06, 2015

Nathan

April 06, 2015/ Jennifer Wesselink
Nathan

Meet Nathan our BWS buddy

Read More
April 06, 2015/ Jennifer Wesselink/ 2 Comments
April 04, 2015

Ali

April 04, 2015/ Jennifer Wesselink
Ali

Meet Ali our BWS buddy

Read More
April 04, 2015/ Jennifer Wesselink/ Comment
April 04, 2015

Jasper

April 04, 2015/ Jennifer Wesselink
Jasper

Meet Jasper our BWS buddy

Read More
April 04, 2015/ Jennifer Wesselink/ Comment
March 18, 2015

Danielle

March 18, 2015/ Jennifer Wesselink
Danielle

Meet Danielle our BWS buddy

Read More
March 18, 2015/ Jennifer Wesselink/ 5 Comments
October 19, 2014

Alyssa a.k.a Puffs

October 19, 2014/ Jennifer Wesselink
Alyssa a.k.a Puffs

Meet Alyssa our BWS buddy

Read More
October 19, 2014/ Jennifer Wesselink/ Comment
  • About/
    • Home
  • BWS Support/
    • Beckwith Wiedemann Syndrome
    • BWS Genetics, AFP, and Scans
    • BWS Resources
    • Tongue Reduction Information
    • Life in the NICU
  • Jacob's Journey/
    • Jacob's Birth Story
    • Tongue Reduction Surgery
    • Feeding Issues
    • The First Year
    • A Day in the Life of BWS
    • BWS & Beyond (The Later Years)
  • Nutrition/
  • BWS Buddies/
  • Products/
    • BWS Bracelets
    • BWS Awareness Shop
    • BWS baby products
  • Donate/

My BWS Baby

Our world forever changed when our son Jacob was born. He came 3 weeks early and everything seemed to be fine until a few hours after his birth when the doctors came into our hospital room and began discussing signs that our son had a chromosome disorder. It was the most difficult situation I have ever had to face.

We felt scared, alone, and helpless. I spent countless hours trying to find resources, support, and learn all I can about his diagnosis with Beckwith-Wiedemann Syndrome.

It is my intent to create a website where parents of children with BWS can find all the information you are looking for because the last thing you need as a sleep-deprived parent with a newborn is to be spending countless hours on google! 

I pray that you may find comfort in knowing you are not alone in your journey with BWS, and that you are able to discover that life is beautiful beyond the diagnosis.

 

 

My BWS Baby

Thank you!

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