Fetal demise...that's what I saw jotted on the paperwork when we went in for a follow-up appointment with the doctor. Fetal demise...perhaps two of my least favorite words. When we had Brady, we got a certificate of fetal demise in the mail. Not a death certificate, which would have indicated that he lived...that he existed...that he was. No, we got a certificate of fetal demise, which seems to indicate that all we lost was a fetus...a bundle of cells...but not exactly a baby.
So now, we are awaiting the completion of this latest "fetal demise." (And it's so crazy to me that there is nothing that distinguishes stillbirth from a miscarriage in medical lingo. They are both losses, and both tragic in their own way, yet also so different.) I am still doing okay, although I am definitely starting to feel more symptoms...physical and emotional. We have a good plan in place with our doctor, which is also reassuring. Although we would still love for nature to take its course, it is nice to know there is a plan if that is not the case.
To be honest, I would much rather go through childbirth ten times over than a miscarriage. Sure, childbirth is A LOT of work...painful...and the recovery is certainly not instant. But at the end of childbirth, you (usually) have a sweet new baby to snuggle and love. Even at the end of childbirth with Brady, we got some time to snuggle and love him, even if we didn't get to take him home. A miscarriage, on the other hand, is a decent amount of physical pain (for me, anyway), a LARGE amount of emotional pain, and you never get to see, snuggle, or love that "fetus" that is now in demise, which of course leads to more emotional pain.
I apologize, I'm not trying to be dramatic, or trying to get anyone to feel sorry for me. I'm just being real...and right now my reality is a bit painful. I also want to give a voice, a face, to this event called fetal demise...or miscarriage. I don't need to be a poster child, but I want it to be okay to talk about...I want people who go through such a thing to have a voice and to find support as I have. I will never take for granted the love and support that has been shown to us, and I simply hope that some day I can pay that forward so someone else maybe feels just a little less alone.
Meet Henry
Henry's Story
Henry Leland Seretta was born on April 14, 2014. This little monster invaded our hearts even before he was born. He was a completely healthy and happy baby, until he started getting an ear infection and colds in mid-October. We finally got rid of the ear infection, but the cold symptoms never fully disappeared. Over the weekend of November 8 & 9, Henry got significantly sicker. He was admitted to Children's Hospital in Omaha on November 10, 2014, and was diagnosed with acute myeloid leukemia on November 11, 2014. He fought hard for nearly two weeks, before passing away on November 22, 2014. This blog depicts our journey through the grief of losing Henry. If you would like to read more about his medical journey, you can visit his CaringBridge page. More photos and community posts can be found at our Hope for Henry Facebook page. Thank you for sharing this journey with us!

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