Our Story

Natalia’s Purpose is in honor of our sweet angels Natalia & Gisele DeSimone. We lost our first baby girl, Gisele at just over 20 weeks in pregnancy in 2020 due to a genetic disorder called Hydrops Syndrome. After genetic testing, we learned that we both carried the same gene that caused Gisele to have Hydrops Syndrome. We were told in order to have a healthy baby that we would have to proceed with IVF so the doctors can screen for any genetic disorders before implantation – that’s exactly what we did. Natalia, our sweet Princess, was considered a “perfect embryo”.

The pregnancy was normal until I had an emergency c-section at 35 weeks 6 days – the doctors were suddenly concerned that she was not growing at a normal rate. She was 3lbs 7oz and 16 inches long. She was sent to the NICU immediately. Just a few days later, the doctors were concerned because her calcium levels were dangerously high. They ordered a microarray panel to rule out a genetic disorder that may be related to her high calcium levels.

Our Story

Natalia’s Purpose is in honor of our sweet angels Natalia & Gisele DeSimone. We lost our first baby girl, Gisele at just over 20 weeks in pregnancy in 2020 due to a genetic disorder called Hydrops Syndrome. After genetic testing, we learned that we both carried the same gene that caused Gisele to have Hydrops Syndrome. We were told in order to have a healthy baby that we would have to proceed with IVF so the doctors can screen for any genetic disorders before implantation – that’s exactly what we did. Natalia, our sweet Princess, was considered a “perfect embryo”.

The pregnancy was normal until I had an emergency c-section at 35 weeks 6 days – the doctors were suddenly concerned that she was not growing at a normal rate. She was 3lbs 7oz and 16 inches long. She was sent to the NICU immediately. Just a few days later, the doctors were concerned because her calcium levels were dangerously high. They ordered a microarray panel to rule out a genetic disorder that may be related to her high calcium levels.

200+

Families Helped

$2k+

Financial Assistance

$30k+

Toys, Supplies & Food

8+

Countries Touched

After 3 long weeks, we finally received the dreadful news that our sweet Natalia did in fact have a rare genetic disorder. Her Chromosome 18 had a deletion & also extra X material that linked onto where the deletion was making it appear to be a fully intact Chromosome 18. According to the Geneticist, we were told that our baby would most likely never walk, talk, or live past age 10. Our whole world began to shatter from that day forward.

As a mother of two sweet angels, Natalia and Gisele, there’s not a moment I take for granted especially with my son, Bentley, & my husband, Paul. During the 4 short months Natalia was here, she taught me more about life & love than anything or anyone could ever teach me.

– Sashia DeSimone | President of Natalia’s Purpose

The following day Natalia was airlifted to Children’s Hospital of Philadelphia (CHOP) because they found a blood clot in her kidneys. We were relieved that she was being sent to CHOP because we knew she would be in the best hands possible. She was immediately put on dialysis because of her renal failure and intubated as well. Miraculously, after a few weeks her kidneys recovered enough to be removed from the dialysis and the ventilator. Her kidneys did not recover fully but enough where things were looking hopeful. The Geneticists at CHOP treat children who have similar genetic disorders that have seen a lifespan exceeding 10 yrs of age with the ability to walk & talk (opposite of what we were told at the previous hospital).

She had a few good weeks where the doctors were considering taking her out of the NICU. Three weeks later we received the devastating news. After reviewing an Echocardiogram they diagnosed Natalia with PVS. They suggested a catheterization to balloon two out of the four main veins. After a successful procedure, Natalia was taken off the ventilator and was a candidate for Sirolimus to prevent her veins from shrinking further.

A couple of weeks later, Natalia had two seizures in my arms. She was then put on seizure medication. We were so hopeful for a miracle, that we were just thankful that she was able to tolerate all the medication. A few weeks later, the doctors informed us that Natalia's veins were shrinking again but it was worse than before. It was now three of her main veins that were being affected. She then had another catheterization. She never recovered the way we hoped for after her second catheterization. We lost our sweet Natalia one day shy of her turning 4 months.

Our Purpose

Cure For Pulmonary
Vein Stenosis

Help alleviate the stress during the holiday season by donating so we can purchase toys, supplies or a gift card for the families residing at the Ronald McDonald House.

Helping Families When Faced With The Unimaginable

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Holiday Wish List Children & Siblings

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     I love that book and share it with so many parents and it has been extremely helpful for them. I thank you from the bottom of my heart, all my love.

Ronald McDonald House

Our Team

Sashia

President

Linda

Secretary

Paul

Treasurer

Sashia

President

Linda

Secretary

Paul

Treasurer

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