Preeclampsia information and Promise Walk~one mom’s story

This is from my friend Sarah. I’ve known Sarah for a couple of years through Philly Social Media Moms, but this year we bonded when we were both chosen to be Shot@Life Champions and we got to spend time together in Washington, DC. Her story is amazing. Amazing in a good way and amazing in a really scary way. I know several women who have lost babies to preeclampsia, and several more who had to have preemies because of it, and the babies had long lasting health issues.

I am so impressed by her and all that she does–she’s just one of those moms who goes and goes and goes. She did this whole knitted hat thing after Hurricane Sandy, because she’s from the section of NY that got hit hard. She also does  a ton of work for the Preeclampsia Foundation in Philadelphia, and of course Shot@Life. All this while working and raising two small kids! I’m in awe of her and happy to share her story. Here it is.

We mothers are so used to being the nurturers and caregivers that very often we make light of what we are feeling in order to continue on with the routine.  So when I woke up 6 days after my c-section unable to catch my breath, with blurry vision and a dull headache I thought I was just tired. I had a newborn and a toddler, I didn’t have time to think something was wrong with me or what I could do to fix it, but my husband Rob insisted I call my OBGYN. 

Hayley was my second baby.  She arrived full term via scheduled c-section on October 25th.  Our little princess had arrived and even my son Derek, at just 26 months old, was thrilled for our family.  I was released from the hospital and spent two days in that post baby honeymoon phase. When I agreed to called my OBGYN I was surprised at the stern immediacy in her voice when she insisted I get to the hospital right away.

My in-laws rushed over and I kissed my babies good-bye trying to be strong but unable to hold back the tears. Derek was going to be a fireman for Halloween that day, plus my brand new Hayley Jane, I needed to be home and dress Hayley in pink and cuddle her…would she forget me? Would we never bond? I didn’t realize then that it would be 3 hellish days till I saw them again.

Preeclampsia.  I heard the word, I knew it had to do with pregnancy and headaches and blood pressure (mine was 220/110)……but I wasn’t pregnant!!!!  There I was, a mother of two, about to be hooked up to a Magnesium IV so I wouldn’t have a seizure or stroke due to preeclampsia and I had NEVER even heard of having preeclampsia postpartum!

A very sweet nurse sat down next to me and grabbed my hand firmly. She asked me to tell her what I was thinking.  I told her, “I’m scared, I just want to be home with my babies and I’m nervous what will happen to me and I’m afraid that I might die”.  That was the honest truth, I was petrified that I would seize and die.

The first night I was on the magnesium I saw 5 of everything. I had to wear an oxygen tube because my oxygen saturation levels kept dropping so low that every time I would drift into sleep I would wake up gasping for my breath. I was pumping every two hours, unable to get out of bed and hooked up to a catheter.

I felt so sick, oh so sick. The magnesium makes you so so so sickly feeling.  After I came off the Magnesium I felt “better”. My blood pressure was still high but low enough that I could go home eventually.

It took a few weeks for my BP and me to get back to normal. I feel so lucky that my preeclampsia story only involves me and that Hayley was unharmed by it all.  Most people aren’t so lucky since Preeclampsia is the leading known cause of prematurity.  

Thousands of women and babies die or get very sick each year from this dangerous condition called preeclampsia, a life-threatening disorder that occurs only during pregnancy and the postpartum period. Affecting at least 5-8% of all pregnancies, preeclampsia and related disorders such as HELLP syndrome and eclampsia are most often characterized by the presence of protein in the urine and a rapid rise in blood pressure that can lead to seizure, stroke, multiple organ failure and death of the mother and/or baby. Swelling, sudden weight gain, headaches and changes in vision are important symptoms; however, some women with rapidly advancing disease report few symptoms.

Typically, preeclampsia occurs after 20 weeks gestation (in the late 2nd or 3rd trimesters or middle to late pregnancy), though it can occur earlier. Proper prenatal care is essential to diagnose and manage preeclampsia. Pregnancy Induced Hypertension (PIH) and toxemia are outdated terms for preeclampsia. Globally, preeclampsia and other hypertensive disorders of pregnancy are a leading cause of maternal and infant illness and death. The Preeclampsia Foundation www.preeclampsia.org the only non-profit in the US devoted to hypertensive disorders of pregnancy, serving the 10 million women worldwide who develop preeclampsia each year.

In the 5-15 years after having had preeclampsia I am now twice as likely to develop heart disease. According to the Preeclampsia Foundation there are an estimated 4.5M US women alive today who are at risk to die from Cardio Vascular Disease or stroke because of their preeclampsia history. Both Hayley and Derek’s future wife are at a higher risk for developing preeclampsia because yes it is hereditary. I have hope that one day we will find a cause and a cure for preeclampsia. I will forever being trying to help in the education of preeclampsia and raise money for The Preeclampsia Foundation.  I am the volunteer walk coordinator for the Promise Walk for Preeclampsia Philadelphia/South Jersey. May is officially Preeclampsia Awareness Month. Won’t you join our walk on Saturday, May 3, 2014 at Challenge Grove Park in Cherry Hill, New Jersey. We walk on Mother’s Day Weekend to celebrate Mothers and Babies!! If you aren’t local to the Philadelphia area you can find a walk closer to you at www.promisewalk.org We can’t do it alone!

Sarah and her family

Sarah and her family

 

Print Friendly

Comments

  1. Meagan says

    Very touching story! I had these same issues. I found out I had preeclampsia at 27 weeks pregnant, put on bedrest right then and there, it then got so bad I also had HELLP Syndrome. Had to go to the drs 3 times a week up, peeing in a bottle and taking it to the Drs. everytime. At my 3x weekly appointment at 35.5 weeks my ob said I had to go over to the hospital and needed to be induced immediately otherwise I could have a stroke. They hooked me up to the magnesium and started the process. Most scariest thing I have ever experienced. I was then in the hospital for 1 week after I gave birth, and on bedrest for 1 week after I got to go home because I STILL had preeclampsia. Now, 2 years later, I am finally healthy again. Doctors said if I were to get pregnant again it could possibly be much worse.

    • says

      Hi Meagan! Isn’t magnesium the worst!! Have you been on the message boards for the Preeclampsia Foundation website? You should check them out so many women on there have found a lot of support and answers. I am happy to chat and hook you up with other survivors that have both gone on to have other children and others that have chosen not to. If you want to email me sarah@finneganandthehughes.com Thank you for sharing your story as well, preeclampsia, although very common, is not often discussed in the whole baby making/baby having experience until it’s too late

Trackbacks

Give us your $0.02

Unless specified otherwise, all posts here are written by the author who is listed. Any post or essay written here is the opinion of that author and only that person, and not any agency or organization they work for or volunteer with unless stated otherwise. Each post stands alone and should not imply support of any one person or group or be representative of the blog as a whole. Some posts may contain affiliate links. If you have any questions, please email us. Traducimos nuestros ensayos utilizando Google Translate, que es lo mejor que podemos ofrecer en este momento. No podemos hacernos responsables por los errores en el contenido o explicaciones, debido a errores de traducción. Este blog está destinado a dar consejos generales sobre la educación especial para ayudar a los padres en la toma de decisiones. Si usted tiene alguna pregunta o inquietud específicos, siempre buscar la ayuda de una agencia de promoción profesional.