Website donated as a Zechus for Efrat Bas Shifra Tanya and all Cholei Yisroellilui nishmas Yisroel Dovid Ben Chaim Moshe and Yehudis Baila bas Yeshaya Dovid.
Website donated as a Zechus for Efrat Bas Shifra Tania lilui nishmas Yisroel Dovid Ben Chaim Moshe and Yehudis Baila bas Yeshaya Dovid

It all starts with words new parents never expect to hear…

“Your baby has Spina Bifida.”

Questions race through their minds:

Will my child be able to function in society?

How can I manage her complex medical needs?

How can I cope with this difficult challenge?

Will he be able to be independent?

Naftali and Simi Rabinowitz, the founders of Keep Climbing, know firsthand what living with Spina Bifida means.

Because they’ve been there.

They were all diagnosed with Spina Bifida at birth.
And they’re still on the journey…

Here’s a snapshot of what that looks like…

Surgeries
0 +
of doctors’ appointments
0 s
hours of physical therapy
0 s
“ Life as a typical teenager is hard enough, but when you add Spina Bifida into the picture, it becomes much more difficult. We had a hard time relating to our classmates. Our classmates were busy worrying about who they would sit with on the bus on the way to trips. While we worried if and how we would be able to attend. Our friends were worrying if their shoes were in style, while we were struggling to find a pair of shoes that would fit and support our feet at the same time. Our classmates were discussing camps and sleepovers, while we had to really think through if it was worth going as there were many accommodations needed to make this a reality. We wished that we could have had someone who truly understood our challenges to help us navigate and cope.”

So how is it possible to:

Survive? Thrive? Smile?

Live a happy, productive life while dealing with all of this?

YES! We can!

Because Simi and Naftali believe their challenges were given to them so they could fill a unique role

Because they are channeling their strengths to help families
and individuals with Spina Bifida thrive.

Because they know they have a goal, a mission, and a purpose.

And when you know that…

there are no obstacles, only opportunities.

So to answer the questions of worried parents:

YES! 

Your child can function beautifully in society

YES! 

He can be independent

YES! 

There is help available so you can manage her medical needs

YES! 

There is support available for other people coping with this too

Keep Climbing.
Together, we can.

Our mission:

Keep Climbing believes that a congenital birth defect should never limit your potential to live the best life possible.

With help, heart, and a touch of humor, they are sharing their vision by helping others to face the future with hope and positivity.

Be part of something great.

Support something greater.