My Personal Fundraising Page

Thank you for visiting my 2020 Promise Walk for Preeclampsia fundraising page. I am grateful for your donations and for your help in spreading the word about preeclampsia. My goal is to help our community raise funds and awareness and save the lives of moms and babies! Please make a donation to support our efforts to fund education and research into this life-threatening disorder of pregnancy.

My story

I was pregnant for 35 weeks when my blood pressure spiked.  I had never had blood pressure or cardiovascular issues before.  My O/B told me to get a blood pressure monitor.  I bought an Omron and monitored my pressure at home.  The O/B had me do a 24-hour urine collection to test for protein. The analysis came out borderline.  I kept monitoring my pressure until the following Friday when I was 36 weeks pregnant.  That was January 23, 2015.

I went to my O/B for a normal check-up that morning.  They measured my pressure and it was high.  My O/B decided to reschedule my upcoming ultrasound from the following Monday to that Friday at the hospital.  The hospital obliged and I drove myself there (a very short drive thankfully).  I went to the ultrasound and the baby looked okay.  They measured my pressure and it was 170s/120s.  They decided to deliver me then and there.  I was supposed to have a planned c-section in a month.  So instead, I had an emergency c-section at 36 weeks.  One month early.

My son was born.  He was rushed to the NICU.  He had oxygen given to him and surfactant.  After this, his health stabilized for a bit.

Meanwhile, I received the preeclempsia treatment as they finally ruled that I had it.  I got the 24-hour magnesium sulfate treatment.  After this, I began to stabilize.

At five days after, both my son and I were going to be released from the hospital but a giant snowstorm caused the hospital to go into lockdown.  Nurses were working overtime.  And no one could leave the hospital.

The following morning, I visited the NICU to see my son and he was doing okay.  I changed diapers, etc. Then, I didn't feel well so I sat down.  We went back to the hospital room.  My blood pressure spiked to 188/133.  The hospitalist got involved. They ran an EKG and O2 set. I passed those.  They struggled for the next few days to find the blood pressure drug combination that would work for me.  My body failed two treatments. I was released three days later.  I spent a week in the hospital.

The same day that my blood pressure spiked, my son stopped breathing in the NICU.  That prolonged his NICU stay for five days and after another breathing episode, another five days.  He was released after 15 days in the NICU.

Since I was diagnosed with a hereditary blood clotting disorder due to the Factor V Lieden gene, I had to inject myself with a needle at least ½” into my lower abdomen, right above the caesarean incision. This caused me extreme pain. For the first week at the hospital, the nurses did this for me. After I went home, I had to do it myself. Every evening for six weeks after birth. I felt like I was cutting myself with a razor, splitting the muscle all over again. Adding insult to the injury. It was torturous.

It took a few months for my blood pressure to return to normal.  I constantly monitored it and was on a cocktail of blood pressure medications for a few months.  I had a pill box to keep track of which medications to take when. My husband regularly ensured it was full and accessible. My regular physician and I slowly titrated me off the drugs. I cleared all medications a week before I returned to work full-time from the maternity leave.

$155.00

achieved

$100.00

goal

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My Supporters

  • Samantha Feldman August 2020 $50.00
  • Heather Sullivan August 2020 $50.00
  • Anonymous August 2020 $25.00
  • Samantha Feldman August 2020 $50.00
  • Heather Sullivan August 2020 $50.00
  • Anonymous August 2020 $25.00