We got some bad news about our pregnancy… #couple #relationships

[x.Kristen.x]

I found out when I was pregnant with my 1st that I am a carrier of Cystic Fibrosis. My kids aren’t carriers thank god. Praying for you guys ❤

[terrimatienzo]

I want y'all to know that I am standing in prayer with y'all. Praying God's Richest BLESSINGS on your BEAUTIFUL family. 💞🙏💞

[positivelyrachel]

I have a genetic condition my mom passed to me without knowing. It makes me really sick. But she and I got closer when I got sick than we had ever been before. Stay positive:)

[winter]

I’m disabled and chronically ill and I wouldn’t trade life for anything. It is a difficult battle everyday. But. Even being in constant severe pain, I love life and I never want to leave it. Your child will be okay no matter what, they just may need extra supports and accommodations and understanding and patience. As long as they receive what they need, they will enjoy their time on this earth!

[gayle]

Praying for negative results. Hang in there ❤

[angelicanewton]

I'm a first-time mom, and I found out that when I was pregnant, I am a carrier for sickle cell disease and spinal muscular atrophy. Both our twin sons are trait carriers for sickle cell disease. My fiancé got tested, and he is a carrier as well for sickle cell disease.

[MissLauraSquared]

Glad you’re finding out before baby girl is born rather than after. My husband ended up being a carrier for hyperinsulinism, which was then expressed in my daughter when she was born. It caused her to have seizures and she would have died the doctors said if we hadn’t caught it. We didn’t know my husband was a carrier for any genetic disorders, so it was scary going through the process afterward, not knowing what was causing my daughter’s seizures. Praying that all goes well for you! 🩷

[mariepatt]

We had the same situation! I’m 32 weeks pregnant now but I also was identified as a carrier for one of the rare diseases when I took the genetic blood test. We have a perfectly healthy 5 year old so we weren’t really too worried. My husband got his test done and isn’t a carrier. All is good! Hoping you have the exact same thing happen 🙏😊

[nicholerich]

I completely understand your worry. My ex and I were both carriers for a genetic disease. Our first child (a son) inherited the disease and passed away. We were told any children we conceived would have a 1:4 chance of inheriting the disease. We had one more child together (a girl) and she was born healthy and perfect. Miracles do happen. Many prayers for your family. ❤

[cherylsorrell]

Sending prayers for everything to turn out well and that Mal has a safe and uneventful pregnancy 🙏🏻

[Nicole-xqvp]

Not the best feeling. I found out I am a carrier of infant deafness and they told me my child could be born deaf. Come the day she was born, the hospital told me she didn't pass her hearing test. I broke down immediately, just for them to retest her and come back and say she's not deaf. Super grateful she was okay - but I know how stressful the feeling can be! Good Luck ❤

[PatriciaWassil]

Prayers for a healthy pregnancy and baby. Prayers over your family. ❤🦋🙏🏻🙏🏻🙏🏻🙏🏻

[laceylove]

Praying for you all ! Keep the faith ! You got this ! 🙏🩷🙏🩷

[taco-Kitty-Bell]

My nephew has CF I knew it by the description you were given. My sis n law had a healthy 1st baby and went on to having her 2nd to find out bam she is a Carrier omg it was a lot turn out her hubby has it and tgere were alot of emotions until baby boy was born. Many years later he is tge poster child for cf thriving and one awesome teenager and sis in law a great mother you do what you can one day at a time..

[brittanyjerome]

I'm 25 and have three rare genetic diseases. The main one being Pompe disease which I get weekly infusions for. Both my parents are carriers which gave me and my sister 25% of of it being passed down. My sister is only a carrier but I have Pompe disease. It's a lot of gray area in the beginning but the more you understand the better it gets. Sending prayers.❤️🙏🏻

[HazyDaisy]

It’ll be okay Mal don’t stress hun try to relax. I like to crochet to relax ❤ either way baby is gonna be okay that’s why they test early.

[sydnigrauberger]

My father died from a very rare disease that does have a genetic component. All 4 of us kids were offered to be tested for the disease but we were warned, PRE Obamacare, that if any of us were positive for the disease, no insurance companies would touch us for the rest of our lives. Partly because of that reality, but more so that this illness isn't likely to affect us until later in life (as it did oir my dad suddenly at 62), we all decided to not get tested for it. Truly, so many other things could happen in life beyond that disease being a health issue for us.

As we have also gone through those feelings and fears of possibly having a super rare genetic disease, I feel for what you are going through right now. Regardless, remember that God has an ultimate plan for you and your family and maybe He is using this possibility along with your public social position to help others faced with a similar worry or possible life reality. 🌹

[Justine-Davis]

Me and my fiancé had the same thing not sure if it’s exactly the same but we definitely both had to be tested in the end. I was the only carrier thank God.

[kirsteenmckenna]

Keep so strong in your faith, my sister was told there would be numerous genetic problem, she prayed & by Gods Grace everything was perfect and still is, he’s a thriving healthy happy now 14 year. Trust your gut, Prayers for Mal, Cam & baby, trust in god along with things his perfect plans. Thinking of you 🙏🇬🇧💙

[dianatorres]

My sister had the same thing. Her partner came back negative. Hoping for the best ❤