I'm so sorry you're going through this, especially that you have to wait until Wednesday. I prescribe a new book and some ice cream in the mean time.
One of the moms from my other BMB had twins, and one of the girls had SB. She started walking not too long ago. Here's her blog, there's some information there: https://erniebufflo.com/
My thoughts and prayers are with you and your family! I'm gonna repeat PP and say that there is so much help/support/treatment options out there. One that the physical therapist I work with uses with the kids she sees with spina bifida is the Feldenkrais method. She's seen amazing results with this, so I would encourage you to give it a look! Let me know if you have any questions about it, too. I'm more than happy to help any way I can!
I read this earlier today and have been thinking about you all day long. I am sorry you are having to deal with the uncertainty and fears. I am hoping you get some answers very soon.
Last menstral cycle 9/09
Initial diagnosis PCOS (11/09)
Provera (x2), P4 injection. Final Diagnosis POF (2/10) Donor ER 8/27/10 -- ET 9/1/10
Beta 9/10/10=BFP! May 6th 2011 - Our sweet little bear was born! FET #2 July 3, 2014 - BFP! M/C @ 9 weeks
I'm so sorry about the news you got today. How scary for both you and your husband. My heart goes out to you and I will be praying for your sweet daughter. I don't know much about this but please keep us updated!
Mother of two sweet boys. One on earth and one in Heaven. Sweet Baby Wyatt 3/29/13-9/10/13
so, I have never posted I just follow along with everyone here. I'm due the 30th of oct. I feel compelled to post though. I have a 4 yr old son that has spina bifida. Your post struck me right in the heart, I know exactly how you are feeling and what you are going through. First off, our geneticist told us SB isn't genetic, the likely hood is perhaps slightly higher because of DH's occulta but we have no history of any SB in either of our families and our DS has the most severe form. It is just a freak thing that happens within the first 28 days of pregnancy. Please don't research right now, it will just cause more pain. Wait and speak to the specialists. spina bifida can sound terrifying but it is not a death sentence. Because it is all mainly issues with nerve damage (from the lesion on the spine) you won't know the severity of her SB until birth. Were they able to see her spine or identify a location of the possible lesion? My DS's is lower lumber, so down on his tailbone. He was diagnosed at our 20 week ultrasound with hydro, spina bifida, clubbed feet and a few other things were mentioned also. At birth he didn't have clubbed feet but did have hydro. He had surgery at 24 hours old to close his back and at a week had a shunt placed. They told us he would be paralyzed from the waist down but if you saw him today you wouldn't know anything was wrong with him! Idk if they mentioned it but the hydro is directly related to the SB so the baby should NOT have any mental handicap. Please feel free to pm me or comment here with any questions you have. At 4, my son walks, runs and has hit every milestone just as any other child would. We deal with some nerve issues but nothing horrible. I am so sorry, I was devastated when we got our diagnosis but everything went so much better than any of the Dr's told us.
I am so sorry you are dealing with this. I'm sure it must be terrifying to hear something like that. I hope your discussion with the geneticist goes well.
Thinking of you guys and sending thoughts your way. I'm so sorry you're going through this.
Started TTC August 2012.
BFP 10/17/12...natural MC on 10/23/12, Missing our little bean every day!
11/13-started seeking help at fertility clinic.
Me: 29 (ovulation/menstrual irregularities, HSG clear), DH: 31 (1% morphology, rest is normal) SHOCKING BFP during cycle prior to IUI #1 on 1-26-14. Beta 1: 39.1, Beta 2: 100, Beta 3: 234.5!!!
keep growing little one! EDD 10/7/14
Sending lots of love to you and your husband right now. Your attitude about loving baby girl no matter what is so inspiring and shows how strong you are.
I am so sorry to hear this! I feel a bit of your pain as our baby has fluid on the brain too. I knew a little girl who was born with spina bifida and against all odds, and multiple surgeries, she was able to walk. Miracles do happen, and people make mistakes - this is what I am hoping for in your case. Keep us posted and you will be in my thoughts and prayers!
Re: Spina Bifida
Married 8/27/2011
BFP #1 9/28/2011 DS born 5/22/2012
BFP #2 4/24/2013 m/c 4/25/2013 at 4w
BFP #3 1/31/2014 DD born 10/14/2014
BFP #4 1/20/2016 m/c 2/12/2014 at 7w2d
BFP #5 8/19/2016 DS2 born 4/29/2017
BFP #6 3/7/2018 EDD 11/18/2018
Last menstral cycle 9/09 Initial diagnosis PCOS (11/09) Provera (x2), P4 injection. Final Diagnosis POF (2/10)
Donor ER 8/27/10 -- ET 9/1/10 Beta 9/10/10=BFP! May 6th 2011 - Our sweet little bear was born!
FET #2 July 3, 2014 - BFP!
M/C @ 9 weeks
<a href="http://www.thebump.com/?utm_source=ticker&utm_medium=HTML&utm_campaign=tickers" title="Parenting Advice"><img src="http://global.thebump.com/tickers/tt1cda00" alt=" BabyFetus Ticker" border="0" /></a>
Fall 2013: Fertility treatments = first BFP!!
07/23/2013 Drew Steven born at 5lb 12oz
02/10/14: Surprise, spontaneous BFP!
EDD: 10/11/2014 Stick, baby, stick!!
Me- 36 DH- 40 ***TTC since 1/13
BFP #1 - 4/3/13 *** EDD 12/13/13 ***M/C 4/12/13 @5wks 1 day
BFP#2 - 1/29/14 ***EDD 10/11/14
It's a GIRL!!!
SHOCKING BFP during cycle prior to IUI #1 on 1-26-14. Beta 1: 39.1, Beta 2: 100, Beta 3: 234.5!!! keep growing little one! EDD 10/7/14
Sending hugs and prayers to you, your DH and your baby girl!!!
Native NYC-ers living in Switzerland - First time parents - 36 + 37
TTC: 8 Months / BFP: 2/8/2014 / EDD: 10/20/2014
Married to M and proud mothers to Olivia and Elise (8/19/2014) and to our fur-babies: Capone (pitbull), Jax and Atticus (cats)