r/GirlDinnerDiaries • u/Little_Emu2309 Blood Type: Gravy • 4h ago
Trigger Warning ⚠️ Devastated by son's diagnosis
My 5 year old son has always been delayed. He's hit all of his milestones significantly later than most kids his age. He's in physical therapy, speech therapy, and occupational therapy. He was diagnosed with autism when he was 3. I was willing to accept this diagnosis. My husband was not. He said it just didn't seem to fit our son. So we started seeing a neurologist who, upon first meeting our son, immediately seemed to question the autism diagnosis. So, we decided to do some genetic testing.
When we found out we were pregnant with our son, we opted not to do any genetic testing or carrier screening when my OB clinic offered. We didn't have a lot of money, and we had no reason to believe anything ran on either side of our families. About a month ago, we got our son's genetic testing results back. He has Fragile X Syndrome. We were shocked. And the more we looked into Fragile X, the more devastated we became. It's an X chromosome linked disorder, meaning it (usually) comes from the mom's side. It's the most common genetically linked form of intellectual disability. Their body doesn't create the proteins needed to be able to learn. After reading stories from other families with Fragile X children and speaking to multiple genetic counselors, it's very likely that our son will never be able to get a job, be independent, have a family of his own.
Because I am a carrier of Fragile X ( I have one normal X and one affected X), each pregnancy has about a 50% chance of receiving my affected X chromosome. Males are much more likely to be severely affected. And just based on developmental and physical similarities, we believe his 1.5 year old brother also has Fragile X. We are getting him tested next week to be sure.
Then we started reading about how females who are Fragile X carriers have a chance of going through menopause early - like in their 30s (I'm early 30s). There's also a chance of developing Parkinsons-like symptoms (tremors, ataxia, memory loss) in my 50s.
And because we weren't dealing with enough already, we found all of this out when I was 16 weeks pregnant...with another boy. We have been scrambling to get in somewhere to do an amniocentesis to test if this baby has Fragile X. We are considering termination if he does have it. I feel so broken and so guilty. I have cried every day and I change my mind every hour. This baby was planned and wanted. But my husband and I don't come from big families. When we go, there will be no one left to look out for our children who will likely not understand what's going on. To subject a third child to a future where we can't guarantee they'll be looked after when my husband and I are gone feels cruel and irresponsible.
My mental health has been absolutely horrible. I feel like I'm already in a state of grieving. I no longer want to see my baby on ultrasounds. I don't want to feel him kicking. It just reminds me that he's there and that I may have to say goodbye to him. I guess I'm just looking for some words of comfort from internet strangers as we face this impossible decision.
Dinner is cajun sausage and beans made in the crockpot.
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u/biscuitboi967 APPROVED✨ 3h ago
I have a friend who terminated a pregnancy due to Fragile X. It was a very wanted pregnancy.
But she already had one daughter - who is likely a bit on the spectrum, but very low support needs and was never diagnosed. Just what you’d call “quirky”. Very high intellect just a little late on some social and behavioral milestones.
For better or worse, she also had a coworker with a son with Fragile X and he was on the more severe scale, already 6 feet tall at 14. She knew that she couldn’t predict the “version” her son would have, and she knew she couldn’t be a proper mother to her existing daughter if she had another, much higher needs child.
Coincidently, my friend also developed MS around the time her oldest was 10. She’s been able to keep it fairly well controlled for the last 15 years, but it meant cutting back her hours at work, maintaining a strict fitness and healthy eating routine, getting sleep, and generally more self care than she would have with a high needs child.
It wasn’t a decision she wanted. It was a VERY EXPENSIVE decision, not covered by insurance. Even in our very liberal state, she had to travel to have the procedure. But it was what was best for her already born children, and what ended up being best for the whole family a few years later when her own health needs became evident.