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Down Syndrome Diagnosis

130 replies

Crazylady1 · 21/09/2017 10:53

Hi, I am looking for people that are or have been in the same situation as us. I am 14 weeks into my 2nd pregnancy and had confirmation last week that our baby will be born with Down Syndrome following a harmony blood test, we were given a 1 in 5 diagnosis that prompted us to do the further testing that lead to a confirmed result.

I have a DS aged 8 with a different partner that was conceived following 7 years and 5 attempts at IVF.

So to conceive naturally was unexpected but a wonderful surprise for us both , this is my partners first child.

Our initial reaction was that we would continue with the pregnancy, however we are now unsure and bouncing between continuing and terminating .

I am 39 and my partner is 41, while we know that we would love, adore and support this child if we continued with the pregnancy, our biggest fear is when the child gets older, how will we cope in our 70's with a adult with disabilities? (if we last that long!!!) We don't want my DS to feel it his responsibility to care for his sibling and we also don't want to be dependant on society but we are a standard family with an average income.

While we know that Down Syndrome Adults can lead independent lives with minimal support it all depends on the severity of the disability and we have no way of knowing the severity of the disability until birth. We have decided that we want to have the 20 week scan to see if there are any further problems that can be detected ie heart / bowels, but even then it will not be conclusive. I think it 's the fear of the unknown, I have spoken to 2 families. 1 has a Daughter aged 13 who is mildly effected, however they said if they had known they would never have gone through with the pregnancy which surprised me as they adore her, another was a distant relative who has a 48 year old Down Syndrome male who leads a fulfilling life but still lives at home and requires assistance like showering and personal care and they would not change a thing... My partner is very supportive and we are talking but he is struggling as am I, We would never judge anyone on the decision they make in this situation, however been in this position we feel lost and know that only we can make the decision for our family. We have spoken with the consultant who is putting us in touch with further families and I am researching as much as I can but how on earth do we make this agonising decision??? any advice / guidance that can be offered would be greatly received. Thanks a Mummy in turmoil

OP posts:
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ohlittlepea · 20/10/2017 06:06

Dolwar. There was no need to put in your post that you are a doctor. Its completely unprofessional. The way you talk about people with DS makes me very sad becayse if that opinion translates in your practice your patients deserve better.

My perspective on disability has always been a reasonably positive one. I think perhaps this depends on how many people who have learning and or physical disabilities that you spend time with growing up/in day to day life. Spending lots of time with people like this means Im not afraid of difference and I have an appreciation. So my appreciation of someone who has Ds is always hoing to be coloured by that. Everyone is an individual and there are people who find the journey harder than others. The local DS support group has been amazing for us. My family member gets free swimming lessons, makaton group, sensory play group, baby massage, physiotherapy, portage and some DLA. They are also entitled to the 2 year old free funding at nursery. There is a lot of help out there. Weve alreasy been sent things from chariyies who offer paid work placements, residential care/supported living in later life and although we cant guarantee these things will be in place for when they reach that age I know that my family and friends will be.
As another poster said even for children who present as healthy/genetically typical on scans this doesnt guarantee that they wont go on to have health conditions or learning disabilities.

UnderTheF1oorboards · 22/10/2017 18:57

MissWimpyDimple children (not babies) with DS do present very differently to NT children. It's not a bad thing. Trust me, when your child is diagnosed you do A LOT of gazing into the future. Will I still be somehow supporting DS1 into my dotage? Probably. Do I mind? Not at all.

MissWimpyDimple · 23/10/2017 22:32

Yes and my aunt would say the same. But the siblings might feel differently.

curliegirlie · 24/10/2017 01:05

Yes, some siblings might feel differently, and some may find things more burdensome than others (my heart goes out to the poor PP who had to act as a responsible adult to their brother at a police station). But not all will experience their siblings with DS as a burden, just as not all find NT siblings with problems or issues meaning they need support as a burden, and I’ve read plenty of positive testimonies from siblings. In my case, I already have a daughter with Down’s and am pregnant with my second. I refuse to believe I am being selfish by having another child, which is kind of the implication from the ‘but think of the siblings!’ posts.

Ttbb · 24/10/2017 01:20

I don't have DS child myself but I didn't want to read and run. I know a family quite well with a DS DD (one of five children). They all seem very happy now (despite initial shock) and are coping well generally (considering that they have five children!) All of their children seem just lovely and happy Fortunately their DD hasn't had many health problems and is generally a healthy, happy girl. I do think however that you raise some very valid concerns regarding your age and the smallness of your family. Do you have any other relatives that you are close to who will be able to step in if sonething happens to the two of you? How are you financially placed in terms of leaving an inheritance for your child to provide financial and care support? Unfortunately with conditions like DS, and life in general, you can never know how things will turn out. If there are no additional complications and both of you live to a ripe old age without any health problems yourselves then that would be wonderful but I think that you need to consider what would happen if things don't go so well. Whatever you decide I wish you luck.

Crazylady1 · 25/10/2017 20:29

Hi All, just wanted to give you an update. We have had our 20 week scan and all is good. We have seen a heart specialist and it does not appear that there are any issues and we have a healthy little boy. After lots of research and lots of conversation DP and U have decided that we are going to continue with the pregnancy. While we both still have fears we have come to terms with the diagnosis. So we are gonna try and enjoy the rest of our pregnancy and look forward to welcoming our DS into our family. Thank you for sharing your experiences with us this has helped.xxx

OP posts:
Four4me · 25/10/2017 20:49

Congratulations!! Super news about the scan.
Our dc1 has DS and has just turned 14. He is an absolute poppet and very much big brother to his 3 siblings. Thriving at MS school, loads of friends, brilliant swimmer and taller than me already
It was a post-natal diagnosis and I do feel sad that I spent a great deal of time when he was a gorgeous squishy baby very sad and shocked. Hopefully you will be able to spend the rest of your pregnancy looking forward to meeting your baby who (whatever his/her extra needs) will teach you and those around you lots about humanity and the important things in life.
There are some brilliant Facebook groups including pregnancy ones if that is your thing.
Good luck x

UnderTheF1oorboards · 25/10/2017 21:02

Great news about the scan OP. Here’s to your lovely family FlowersFlowersFlowersFlowersFlowers

curliegirlie · 25/10/2017 23:48

Lovely news! Welcome to the club, congratulations and good luck!

Happyflower74 · 05/11/2017 21:14

I was just flicking through and came across your story. I wondered how you’re getting on? My little girl (now almost 5) has DS and we knew this was very likely from the 12 week scan. Pregnancy takes forever and even more so when you have other things on your mind. I just wanted to encourage you and check that you are being supported enough. There are loads of brilliant support groups for when you’re ready and a new website www.positiveaboutdownsyndrome.co.uk that you may find helpful as it has different stories written by Parents for Parents. If I can be of any help to you or you need any information just shout! Congratulations and I wish you all the best for your last few weeks.

LorraineBuck · 11/11/2017 10:51

Hi. A little late to your post but can I just say a huge congratulations on your pregnancy.
I am a mum of 5 amazing children. My youngest is now 3 and has Down's syndrome.
I remember the fear throughout my pregnancy and reading posts like this.
My son has no health issues. He was born 4 weeks early as my placenta failed but was a good weight. He exclusively breast fed for 19 months. By far the easiest of all my children he is adored by everyone who meets him.
Make sure you take every therapy offered. Speech, physio, portage. Healthcare in this country is amazing. He gets a yearly medical, hearing and sight tests 4 times a year, despite no problems.
He was a little bit slower achieving milestones. Sat up at 11 months, walked at 2years 2 months. He rarely cries and lights up the lives of all who meet him.
my son's siblings all adore him. He is perfect just the way he is.
If you would like to see our journey, he does have a Facebook page. Jaxon Rio Buckmaster Life's ups and Down's.
I would be happy to point you in the direction for any help and advice.
Positive about Down's, Future of Down's are all good places to start. Congratulations again.

Crazylady1 · 01/03/2018 18:08

Hi all update is we
are proud to announce the Birth of our son on 21/02/2018 at 21:03 pm weighing 7lb 7oz Harry made his appearance into this world. We are completely besotted with our perfect little boy, he has a alight heart defect that we are waiting to see the specialist for , otherwise he is for and healthy 😍👶😊 xxxx

Down Syndrome Diagnosis
Down Syndrome Diagnosis
Down Syndrome Diagnosis
OP posts:
Clarabumps · 01/03/2018 18:14

Congratulations!! He is absolutely beautiful! Enjoy your newborn cuddles. Best feeling in the world. Xx

onemoremummy · 02/03/2018 07:56

What a precious little boy! So happy for you and your family. Xx

NorthernLurker · 02/03/2018 07:59

Harry is simply gorgeous. Congratulations.

Bl7589 · 02/03/2018 08:06

This reply has been deleted

Message withdrawn at poster's request.

Spottytop1 · 02/03/2018 08:20

Congratulations on your gorgeous little boy. Smile

TheVeryThing · 02/03/2018 08:24

What a beautiful little boy. Congratulations

fairgroundsnack · 02/03/2018 08:24

Congratulations! He is gorgeous. Did you get in touch with Sarah who writes Don’t Be Sorry? She is lovely x

Flywheel · 02/03/2018 08:26

Congratulations. He is wonderful

yumscrumfatbum · 02/03/2018 08:27

Many many congratulations xxx

catinboots3 · 02/03/2018 08:58

Congratulations OP XX

NoKnownFather · 02/03/2018 08:59

Congratulations Harry, wishing you all the best for a wonderful life. You have great parents. Flowers

Ski40 · 02/03/2018 09:29

No proper advice from me I'm afraid but didn't want to read and run. You sound like a lovely family and whatever you decide will be for the best.
I also lost a baby girl to Trisomy 18 (Edwards) so I know the misery of genetic problems but at least I didn't have to make a decision as nature did it for me 😢.
My heart goes out to you xx

Smellyjo · 03/03/2018 09:00

Welcome Harry! He is beautiful op. Congratulations to you all. Xx