WENDYFOREVER is my personal blog dedicated to my daughter, Wendy. When I was 15 weeks pregnant, our daughter was diagnosed with Anencephaly, a rare neural tube defect and was stillborn last November.
I was told something no mother should ever hear, "Your baby is not compatible with life."
This blog reveals the nightmare I had to live through, the dreams I was forced to let go, and the hardships I have to overcome. But, also, the grace that saved me, the love that held me, and the wisdom that grew me.
I aspire this blog to bring others hope, a helping hand, or an open ear.
I am not a pastor, doctor, nor a therapist, just a bereaved mother wanting to share my story - her story. My Wendy.
While scrolling through my Instagram feed I found this beautiful illustration stating, “You are worthy, even when you don’t feel like it.” That struck me like lightening, but also provided a sense of comfort. Since the loss of our daughter Wendy, my life seemed uncle...
This is a season of new life. Spring is my favorite season of the year with freshly bloomed flowers spotting the green earth. Bees and butterflies dance and flutter in the breeze. I love the sound and smell of light showers falling from full clouds. Near my town, t...
wendyforever is place to share my story. Well, more accurately, my daughter's story. I wanted to create a place where I can express myself as some sort of a therapy, while helping other mothers who might be going through tough times as well.