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About wendyforever.

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.

You see, I always wanted to be someone that people could look up to. Someone that people can go to for advice, help or wisdom. I wanted to be someone that listened. Because I care and I know there is a need out there which has morphed into a taboo.

Pregnancy and infant loss is very real and so many have experienced this nightmare.

But, I want to let you know that you are not alone.

I want to share my daughters story to give others hope, because this world is pretty messed up. And life can get very very difficult.

My daughter Wendy was born last November on the 12th at 12:17pm. I carried her for 41 weeks and she weighed 3 pounds 10 ounces.

You may thing, "That is a tiny baby for it to be carried for so long." And you're right.

My daughter was diagnosed with a rare and fatal defect that was not "compatible with life" - as doctor's would say.

You can read her story here, but I wanted to let you mother's know that...

You matter.

Your baby matters.

No matter how big or how small.

You baby is precious and has lived.

You are not alone, I am here and I see you.

With much love,


#anencephaly #pregnancyloss #newbornloss #childloss #stillborn #bereavedmother #ntd