Colorful chalk drawing on a pavement with text '1P36 Deletion San Diego 2016 #1p36strong'.

Introducing

The Noah Project

Postpone to the future

Our Mission.

The owner of this company has someone special in their life with 1p36 Deletion Syndrome, and his name is Noah!

We want to take this opportunity to help others with the same rare disease.

Thus, the Noah Project was created in 2025!

What is the Noah Project? 

It is simple!

The Noah Project is an opportunity for our company to raise funds for research on 1p36 Deletion Syndrome.

What is 1p36 Deletion Syndrome?
 
In simple terms, 1p36 Deletion Syndrome is when a person is born with one less chromosome in each cell. 

Some people are born with missing body parts, while others can have several diseases along with 1p36DS.

Unfortunately, we cannot show his face, but Noah is a smart cookie! 

The owner learns several things about the disease by going to one of their once-a-year conventions since 2009. 

The owner saw many children with different types of missing limbs. Some were born without legs, vision, heart disease, underdeveloped organs, and more. 

At the convention, the owner learned that 1p36 Deletion Syndrome is unknown to 1 in 10 individuals born with it; the syndrome was discovered in 2007. 

Several children need surgery to continue living, and others have died due to a lack of funds to receive surgery.

Thus, the owner has decided to make the Noah Project page.

We hope to give a donation price to 1p36 items to help children who need surgeries such as heart surgeries, and more.

The goal of this Project is to raise money to be sent to 1p36DS yearly on Noah's birthday month! Each year, in the first week of September, the owner wants to donate items and send money to the 1p36 Deletion Support and Awareness Program. 

We are asking people to donate the amount listed under each item.

Please be aware that the donation prices will be twice the original amount.

We hope you can donate to the Noah Project. 

We eagerly await your support.

Sincerely,
-The CeCelia Team

Here is the link to learn more about this rare disease. 
https://www.1p36dsa.org/

Donate
http://www.1p36dsa.org/donate-now/.

Products are not available at this time.