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Post On Thursday, March 08, 2012 By TaMyra
This is my story of survival. This is also my daughter's story of survival. At 22 weeks, I noticed my feet were extremely swollen, and I could barely breathe. I thought it wasÃ‚Â just normal pregnancy symptoms, until the doctor said myÃ‚Â BP was 170/11!!Ã‚Â I was diagnosed with pre-eclampsia at 23 weeks. It was way too early to have my baby. We were given steroids immediately for her lungs, in case an emergency C-Section was needed. I was also given Magnesium sulfate, so I wouldn't seize. This medicine made me feel like I was dying.Ã‚Â I was put on bed rest and admitted to the hospital. I watched myself gain 5 pounds a day for several weeks, to the point where I reached 276 pounds at my heaviest.
This gave me an extra 110 pounds of fluid in 5 short weeks. My body began to break down, while my organs worked extremely hard to keep me and my baby girl alive. The days turned into weeks, and every hour became critical for our survival. As week 32 approached, I was expected to be induced, but still being 5 days away, I couldnÃ¢â‚¬â„¢t take it anymore. I prayed and God told me it was time. I told the doctor it was time, but he wasnÃ¢â‚¬â„¢t in alignment with me. I knew it was time, so I proceeded to head over to another hospital, which happens to be where I was born. Immediately after being admitted, I was in the OR and prepped for an emergency C-Section. We are all nervous that the fluid would fill my lungs after delivery. The doctors had never seen such an extreme case of pre-eclampsia like this in over 20 years. After delivery, my baby girl had to be resuscitated and weighed in at 2lbs 13.8 oz. SheÃ¢â‚¬â„¢s surely a fighter because she pulled through and didnÃ¢â‚¬â„¢t even need to go to the NICU, but the Special Care Unit, which is a step up from NICU. For me, this was not such the happy ending. My body immediately crashed. I was then diagnosed with Kidney Failure, HELLP syndrome, DIC, and many other conditions. The next 48 hours were extremely critical for me. We counted on the fluid to come off fast, but since my kidneys were shutting down, dialysis was my only option to fight for me life. Blood transfusions were also administered because my blood wouldnÃ¢â‚¬â„¢t clot. After days passed by, I had yet to see my angel for the first time. Jordin Marie Dawkins is what we decided to name her, while Angel Face became our nickname for her, since she was such a blessing to be alive. After weeks of therapy, I was finally able to leave the hospital and continue my recovery at home. I had to learn how to walk again and use my limbs because the severity of fluid caused most of my muscles to break down.Ã‚Â Even though it seemed to be over, 3 years later, it still is not over. I live every day with reminders of what we had to endure. I worry for my daughter that she may experience similar conditions, since there is evidence that my mother, also, had this disease. My passion in life is to bring as much awareness to this disease, and ensure women are educated on the symptoms and looking for these signs. It's also time that researchers spend time and resources to understand any historical data that may help prevent, fight, and cure this disease that kills so many mothers and babies.
Ella was born prematurely on 6/5/09. Due to her premature status she was required to stay in... Read More