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Down Syndrome - help needed please

13 replies

fairydust · 28/01/2008 14:18

Need help / info we're to look etc

My little sister was called back into hospital today for an emergency scan and had been told that she has a very very high chance of her little boy havin downs...

ALready most of the family are tellin her she should have a abortion which has caused me to fall out with most of them - i have little girl with Cerebal Palsy so know how hard / rewardin it all can be -

so i promiced her i'd arm with with as much info as poss to make the right choice for her
so this is we're i need help / pointing in the right direction please

many thanks in advance

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heartinthecountry · 28/01/2008 14:23

fairydust - have you done an archive search? There are threads on this topic fairly often with some great advice.

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2shoes · 28/01/2008 14:26

keep bumping someone will come along.

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sharonkitten · 28/01/2008 15:07

Hi Fairydust

My little girl has DS - she is 3yrs old now. What is it you want to know? my dd's website is www.constanzesmith.com if you wanted to take a look/pass on the link.

Also a useful info website www.downsed.org

If you or your sister have specific questions then i will do my best to help - my email is [email protected]

Sharon x

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welovetelegraphpoles · 28/01/2008 16:52

This reply has been deleted

Message withdrawn

RTKangaMummy · 28/01/2008 17:08

My best friend has adopted 2 children with DS

Her DS is about to be 16 years and her DD is 9 years old

They are deffo brill

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theheadgirl · 28/01/2008 18:01

Hi fairydust - my DD3 has DS. I found out at 19/20 wk preg that there was a high chance of this, due to blood test results. I decided against amnio as I knew I couldn't terminate for Downs. I couldn't terminate for many things, especially at that late stage in pregnancy.
My daughter is now 7, a beautiful girl, one of 3 beautiful girls and I can't imagine my life without her. It is a different life to the one I'd be leading if she didn't have special needs, but I wouldn't change her. I'd recommend getting in touch with the down syndrom assoc. and also meeting up if poss with families who have children of all ages who have Downs. For me, this "normalised" the situation, to see families where one of the members have SN, just getting on with things, and being Happy.
All the best to you and your sister xx

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yurt1 · 28/01/2008 18:05

Gosh fairydust that must be hard for you- having the family all talk about termination when you have a disabled child yourself. Do search on eidsvold's name- she found out at a scan that her dd1 was likely to have DS (she does - and her story is interesting because she was given a bleak outlook re heart defects at the scan- after birth it was discovered the heart problems were not as bad as predicted. Medics tend to look on the bleak side I find).

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twocutedarlings · 28/01/2008 19:08

fairydust Eidsvolds actually post here today about her DD starting school today.

Take a look at the picture on her profile, and of corse headgirls profile....now you dont get kids much more cute than that .

My friend DS has down, and other that a 6/12mth delay in most area (walking, talking ect) he has done extremely well. He has no major medical problem. He has a very minor heart defect but this could infact be an inherited one and actually be nothing at to do with her DS.

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fairydust · 28/01/2008 22:12

thanks all i really apreciate all your posts - i have read many threads over the yr but when its happening in your life it kinda become more of a reality.

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eidsvold · 29/01/2008 03:56

It must be a really tough time for you and your family are being incredibly insensitive and ignorant.

It is hard for me as she was just our baby and we decided no matter what she would be born and we would take it from there.

We found talking to parents of children who have down syndrome so helpful. We wanted to know the day to day reality.

You can contact the DSA - UK. I know dh had quite a long phone call with them when dd1 was born.

down syndrome assocation

As Yurt said we knew before dd1 was born - she had a complete AVSD ( heart defect) and down syndrome. At 8 weeks old she had two open heart surgeries and is doing great. Unless you saw the scar you would never know.

There are a lot of posts I have written about down syndrome.

the link on this thread is BRILLIANT

There are some pics on my profile - of her at a couple of weeks old, a few during her life up til now and in her school uniform.

This morning she started school - she was in her element. Me I cried like a baby!!!

I'll see if I can find some of my threads or posts for you to share with your sister. If you want to CAT Me I can pass on an email address for your sister to contact me if she wants.

I also found this helpful - it was written by a parent who had a child with down syndrome.
I think it really describes for me what it is like to be dd1's parent.

here

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eidsvold · 29/01/2008 03:56

oh I found a post about dd1 - so apologise in advance for the length:

right - dd2 and 3 having a sleep - some time to post.

As someone else said - we basically knew antenatally that dd1 would have down syndrome. We also knew this was our babe and she would be born - we would deal with the rest when the time came iyswim.

We learnt at 20 weeks antenatally that she had a heart defect that was very very common to children with down syndrome. We were in fact told that it would be very very rare for her to be born with the heart defect and without ds.

Knowing beforehand and making the decision to have dd1 does not mean there were no tears, grief etc. We had her down syndrome confirmed in a very poor way - dragged into a corridor in SCBU where dd1 was in intensive care, a registrar shoved a piece of paper under my nose, tapped it, nodded at me and then shut the folder again. Dh could not see a thing.

I can tell you - I wept - like I had never wept before - even antenatally I was not upset as I was at this point in time. However it could have also been the day 3 or 4 hormonal crash that comes post birth. I wept for my babe who would face a world that would never see her as 'perfect' although to us she was perfect, I wept for the imagined slights and hurts she would suffer, I wept thinking I would never be a good enough mum for this wee thing. I thought I was too selfish, impatient, weak and would expect more than she was able to give.

Boy was I wrong - but enough about me. She has overcome things that just amaze me. At 8 weeks old and just 8lbs she had two open heart surgeries a couple of days apart. She fought back from a rocky recovery and to look at her now, unless you see the scar you would not know.

She is gradually reaching her milestones - she seems to take a little while but each new skill grasped/learnt is another cause for celebration just as it is for her two sisters.

At 5, here in Australia she attends a mainstream kindergarten and is off to mainstream school next year. She also attends a special needs unit and that will be part time next year transitioning to full time mainstream. She attends swimming lessons which she adores - she is my water baby.

She is mastering the flying fox at the local park, as well as climbing like a monkey with no fear whilst I sit with my heart in my mouth - learning to sit back and give her space. She was almost 3 when she learnt to walk now - she runs - anywhere and everywhere grin I always joked she was my olympian swimmer, I am revising that dream to her being my olympian sprinter!!!

She is the funniest thing - she has a wicked sense of humour and a laugh that comes from her boots - she wishes no ill towards others despite it being displayed to her. She relishes seeing other people - outings are to her adventures to meet other people and learn about them.

We have met so many amazing people because of dd1 and the fact that she has down syndrome. We have had amazing experiences - both trying and elating.

She is an important part of our family - her two younger sisters adore her. To dd2 - all she wants to be when she is bigger - is dd1. Dd2 does not see anything wrong with the fact that she is toilet trained and we are still working on it with dd1, she does not see that dd1 is not as verbal as she is - to her dd1 is her partner in crime, her mate, her darlin ( as she sometimes calls her). Dd1 in turn adores her two sisters. Earlier in the year we had a babe and dd1 was beside herself - she did nothing but talk about the babe at sn and mainstream kindy and to anyone that even looked sideways at dd3 in public.

As to how you cope - one foot in front of the other, one day to the next - I work on the stage I am at and then we work on our progression. For me that is how I 'cope' but to be honest yes there are some issues but as a babe - she was much easier than dd2 in terms of day to day care. Even now she is less demanding in a lot of ways than dd2. I know some parents cope by looking long term and getting that sorted BUT that is not me. I work on the here and now. I get through today and then work on tomorrow.

As I said in my earlier post - this sadness is normal - BUT that subsides and the love for and bond you have with this babe will take over - you will be besotted as we all are with our babes.

I knew when dd1 was born my life would never be the same - and you know what - I was right - I feel so blessed to have my three beautiful girls and the privilege to be dd1's mother - even when she is stomping her foot and telling she does not want to clean her teeth grin.

You will dream new dreams and very shortly you will reach a point where you cannot imagine life without your dd.

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fairydust · 29/01/2008 12:39

thanks for that eidsvoid sister phoned in floods of tears this morning she said she loves her new baby so much and i said we'll there's your decision and she said yeh your right so bump is now called joey and wether results come negative or positive i'm going to have a beautiful nephew

she is still going to come over to mine and read through some posts

so once again thanks all xxx

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yurt1 · 29/01/2008 12:43

awww best of luck to her. I've said this on here before but this time next year she'll have a baby who she loves- no matter whether her baby has DS or not. This time next year it won't make any difference to her.

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