MY JOURNEY FROM MEDICAL MISDIAGNOSIS TO THE PRESENT

GUEST BLOGGER: Lorina Troy

This September is National Hydrocephalus Awareness Month and I felt like it would be the right time for me to tell my family’s story.

Due to a medical mis-diagnosis, my family has been through un-imaginable life-changing and unexpected circumstances. In May 2015, because of that misdiagnosis my children were taken from me and my husband. My sons were placed into foster care for five months. Our family was railroaded by false accusations. Doctors quickly gave an inaccurate diagnosis which has greatly affected our lives.

It is vital for physicians to exercise due caution when their diagnosis will affect the child’s treatment and the way in which hospital staff and others will treat that child’s parents. Now, I would like to raise awareness for cases in which a diagnosis of Hydrocephalus was not made, the medical consequences for the child and the impact it has had and continues to have on families.

The worst day of my life was when our children were wrongfully taken from us and put into foster care. My heart broke as I watched my boys crying as they were taken. Each day I missed my boys. The silence of the house was deafening. Charges of abuse were filed against my husband. We had to hire one attorney after another hoping to find the one attorney who would defend his innocence, discover my son’s correct diagnosis, and give my husband a way to restore his good name.

My husband earned his Bachelor’s Degree in Criminal Justice and achieved a top-secret clearance with our government and military. When he had to leave his job with the government he felt betrayed and lost his faith in his lifelong icons of truth and justice. We had to sell our house to pay the attorney’s fees. We were blessed to have very large and generous families who readily provided their support. My husband and I, as well as my two boys continue to heal from the traumatizing events that all began with the physician’s failure to correctly diagnose my youngest son.

There were times when the loss of our children, the unbelievable accusations against my husband and the feeling that we were powerless to right the wrongs – were overwhelming. But, we went through the most challenging events of our lives and it has made us stronger. Now, we can take our terrible situation and what we have learned, and help others in similar situations. Our strength came from our faith, our prayer and the love and support of family and friends. Despite the extreme challenges of our circumstances we had to stay strong and not give up. We believed that a Miracle of Faith would happen.

Over a million people are currently diagnosed with Hydrocephalus. There are different types of this condition. My son has Benign External Hydrocephalus of Infancy, in which there is an abnormal build-up of cerebro-spinal fluid (CSF) outside of the brain. Benign External Hydrocephalus is present at birth and may be caused by either events or influences that occur during fetal development, or genetic abnormalities, or a complication at birth. Acquired hydrocephalus develops at the time of birth or at some point afterward. This type of hydrocephalus can affect individuals of all ages and may be caused by a complication at birth or disease.

I would like to raise public awareness about Medical Misdiagnosis, the delay of needed treatment, the life-altering impact on the family of the patient, and to help other families going through a similar ordeal.

------------------------------

by  Lorina Troy, (guest blogger) a loving mother of two, is the author of Miracles of Faith: Our Child Was Misdiagnosed and It Greatly Affected Our Lives, also available on her website at https://lorinamtroy.wixsite.com/lorinatroy