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Pregnancy

Talk about every stage of pregnancy, from early symptoms to preparing for birth.

amniocentesis

170 replies

Melly · 30/10/2002 12:48

Hello everyone, hoping that some of you might be able to offer some advice or share your experiences on amnio. I am due to have one tomorrow and will be 16 and a bit weeks. I had an amnio when I was expecting my dd and thankfully all was well. This time round I seem to be even more scared, even though I know what to expect etc. Apart from the obvious worrying about the result, the thing that is worrying me is coping with my dd after the procedure. I've made arrangements for her to stay with relatives tomorrow and over night and will collect her on Friday pm which should give me a good chance to rest as they advise you to do. I'm wondering how long you are at risk after the procedure? DD is toddling now but still has to be picked up, carried up the stairs, lifted into her cot etc etc. Is there anything else I can do to minimise the risks? I am also getting myself into a complete state worrying about the result, which I know I have no control over, I was 37 when I conceived and am 38 now. Would be really grateful to hear from anyone.

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susieblue · 03/01/2003 15:03

Jodiesmum, I'm really glad the info I gave you was what you wanted to hear, it was exactly what I was told at the time and am glad you feel a little more at ease. Incidentally, I had my results within 72 hours which I presume you will have too unless of course the weekend gets in the way! Yes, I hope the second time round birth stories are true in that they are suppose to be a little easier but I suppose we do get ourselves into these little scrapes! Take care.

Jodiesmum · 04/01/2003 13:01

Hi again Susieblue, I got my results last night - only 24 hours after the amnio! What an amazing service - it's so quick I can hardly take in the good news - 98% of abnormalities ruled out. Now we just have to wait for the final results though even I find it hard to get worried about the last 2% of problems. Hopefully i can just chill out and enjoy the next couple of months before I get to the big and heavy stage. Thanks again for your support and help.

susieblue · 04/01/2003 23:03

Jodiesmum, great news with regard to your results I had exactly the same result 98% of abnormalities ruled out with a wait for the final 2%. In fact the hospital, I believe, said they would only contact me if there was a problem but they never called! That last 2% is for abnormalities so rare I dont think we would have heard of them is what the lady told me when she phoned the results through. Yes, chill out and enjoy your middle months before you get to the "heavy" stage I really have forgotten how uncomfortable it is and not trying to gain sympathy am suffering from severe carpel tunnel syndrome which affecting my life night and day and has been from week 30!!! Absolutely nothing working as it so severe, maybe natures way of getting me prepared! Take care and enjoy yourself now.

jessi · 04/01/2003 23:44

Brilliant news Jodiesmum!

bundle · 06/01/2003 16:26

jodiesmum, that's brilliant news, you deserve a nice big treat

eidsvold · 10/01/2003 10:14

My husband and I are the proud parents of a beautiful baby girl. She is just over 5 months old. At 20 weeks she was diagnosed with a congenital heart defect - basically she had no central wall between the two sides of her heart. We were also told that this type of heart defect was very common in children with down syndrome.

We were then offered an amnio and I refused. For a couple of reasons - the more I read about amnios the more I am concerned about the outcome particularly the loss of 'normal' babies through miscarriagec- are we endangering babies' lives because we are worried about not having the 'perfect' baby as the media and society tells us we must have. I sometiems wonder why more women don't say enough - to the doctors and to science?!?! I had also decided when they originally told us our daughter possibly had a more severe heart defect that I would not rob my family of this life. No matter what we would have this baby and we would fight for her survival. An amnio would not have changed our minds so we were not prepared to take the risk.

A number of people questioned that decision. But a friend of mine put it into perspective. She said of her little 4 yr old - M could be hurt tomorrow and suffer dreadfully - what do you do then - hand her back - say sorry I don't want her?

Today after an emergency caesarean, three weeks in special care, two open heart surgeries and all the complications you could imagine - I only have to look into the beautiful face of my daughter, see her smile and know I would not change anything for the world. I won't deny it has not been an easy road and it has taken all the strength my husband and I possess to get through this. That little life has touched lives around the world - friends of friends who prayed and supported my husband and I through this all - in England ( where we live) In Australia ( where my family is) and the US where we have friends. She will continue to touch lives.

And yes - that gorgeous girl does have down syndrome.

Rhubarb · 10/01/2003 15:44

Thank you Eidsvoid! That was really nice of you to share your story with us. My sister has a baby boy who had the same heart defect as your daughter, and who also has Downs Syndrome. She found out when she was pregnant too, they actually offered her a termination at 7 months!!! Looking at him now I don't know how the doctors could have ever thought of terminating his life. It has been a struggle for my sister and nephew and will be for some time, but he is more than worth it! We are all very proud of them as your family must be of you!

All the best! xxx

Lindy · 10/01/2003 21:07

Yes, thank you so much eidsvold for telling us your story; I also have a nephew with downs and heart problems and understand (a little) the difficulties - but also the love and enjoyment - involved; I wish you and your family every happiness for the future - and welcome to Mumsnet!

Tortington · 10/01/2003 21:24

fabulous story

geriatricmum · 04/01/2006 13:14

Hi looking for some advice. I'm having my amnio Thursday morning, and my gyane has scared the beejesus out of me by saynig I can't move / travel for 5 days, that's the recommendation. Thing is I have a long planned family engagement over the weekend which means driving 4 hours Friday night, 4 hours Sunday, plus of course being some distance from my hospital all this time. What sort of advice do people normally get on resting after an amnio?

thanks

Normsnockers · 04/01/2006 13:40

Message withdrawn

geriatricmum · 04/01/2006 13:57

yeah, I think the amnio's probably the most important thing here so I'll do it. But why can't you drive after 2 days, sounds crazy to me, its not like it's surgery or something....

pacinoFanOfBrusselsSprouts · 04/01/2006 15:12

No, it isn't surgery but it IS a 'significant interference with your pregnancy' according to my pregnancy book by Dr Miriam Stoppard.

I have recently had an amnio too and my advice would be to rest as much as possible. I was actually pretty shaky afterwards and rested in bed for 48 hours. I wouldn't recommend all that driving, even as a passenger. I would follow your consultant's advice, even if it means you have to miss a family get together.

Best of luck for Thursday, hope it all goes well for you.

natmeistergeneral · 04/01/2006 15:59

i had my amnio in2004 and i was advised to rest for 48 hours (which i did-flat on my back mainly!)then told to take it easy for the following 5 days or so. Can i just add that considering i hate needles and hospitals the whole proceedure was a breeze!

Louba · 03/03/2006 14:57

Hello everyone, pleased to read how many of you have had good results from amnio tests. I had one last Wednesday after much trauma and deliberation due to my 20 week scan showing a marker for Downs that doubled my risk. I knew I would be worrying for the next 4 months if I didn't know for sure. The consultant who did the procedure was very abrupt and although she said she would put my results forward for FISSH testing (results in 48 hours) I found out from the midwife that the consultant had FORGOTTEN to mark my sample, so I'm STILL waiting for the results 10 days later! Wouldn't mind the wait if I had been prepared for it in the first place, and not promised a 2 day result! Am really angry about it, as it's a horrible enough experience! Anyone else had a similar experience? Am trying to think positively, but the longer it goes on, the harder it is...
PS Am 24 weeks PG with first baby and 31 years old.

wools · 03/03/2006 15:09

Hi Louba, No real experience of having to wait as long as you - luckily my consultant did request the 48 hour results. TBH I found 48 hours an eternity - goodness knows how you must be finding the wait..... My ds was also showing soft markers (brain & bowel), so I agreed to have the amnio. Thankfully everything was fine and he is now a healthy 8 month old. I am pregnant again, and I know that they will insist on performing an amnio(because of my age) and tbh I'm not sure how I really feel about it....
I'm sure everything will be okay and it will hopefully mean you can relax for the rest of your pregnancy.

syd1999 · 17/04/2006 00:56

I'm having an amnio on May 1st...and I'd like to know what it feels like??? I've read about many different experiences and some say it was a breeze and some say it hurts when the needle is coming out...some say they felt crampy and weak after it...I just want to know what to expect??? I'm not afraid of pain, I just think the idea of a needle going into the sac reminds me of a balloon being popped by a needle...it's more psychological for me...how doesn't SOME fluid leak out??? Please fill me in if you've had one...Thanks :)

givemeachance · 18/04/2006 15:22

I’ve only just come across this topic but have read it with great interest. I think that while the decision to terminate a pregnancy on the basis of a severe disability must be the most agonising one, and one which I have tremendous respect for, the more advanced science becomes, the more people will terminate pregnancies on the basis of even minor imperfections. In fact people already do, some may remember the case recently where a reverend tried to take some doctors to court because they had performed a termination at 26 weeks for a baby with a cleft lip?

My story is this, and before I tell it I would just like to point out that I am a regular on here, but have changed my name.

I have been totally blind since birth, when searching for a diagnosis, the specialists simply said that it was “corticle blindness” which basically meant that there was nothing wrong with my optacle nerves or my eyes, but that something in the brain was preventing the messages getting through to the brain. However, no one could ever actually tell me why I couldn’t see. There is apparently a name for it which basically just means that it’s one of those things that happened. It is very rare, and there is a list of people with the condition as there are so few in the world. Anyway, apart from being totally blind I have no other disabilities. However, because I was blind my mother then said that she would never have any more children because she didn’t want another baby with a disability. Then when I was 7 my mother fell pregnant, it wasn’t a planned pregnancy, she’d been talking about getting sterilised for years but never got round to it. We were all involved in the discussions about the pregnancy and what was going to happen, how my mum felt that she didn’t want another baby with a disability, even though doctors had told her the chances of having another child with something wrong were minimal as I had no genetic condition, and there are no genetic conditions in our family. She just didn’t want to risk it and so she had a termination. We all knew (bearing in mind I was 7 at the time) that mum was going into hospital to have her baby taken away. I remember going to school and telling a friend that my mummy was expecting a baby but she didn’t want it and so she was going to have an operation and then they were going to take away the baby.

As a small child this had a minimal impact on me, but as I grew up the implications of what my mum had done hit me very hard. For a very long time I felt responsible for the loss of that baby, if I’d been able to see then she would have had the other baby and would never even have considered having a termination, I had a sibling that I never got the chance to know because of my disability, thus, in my mind, it was my fault.

I totally understand why someone who has a baby diagnosed with a very severe disability might make the choice to have a termination, after all, as someone said it’s a life changing thing, but some disabilities are not that severe and do not, imo, warrant terminating a pregnancy. I am now 32 years old, I live with my DH and my 3 year old DS, and we are currently ttc for our second baby. I am totally independent, there is nothing, apart from driving a car, that I cannot do as well as/if not better than some who have sight. I do not have to rely on anyone for anything, and if my mum had had another baby with a visual disability that child would be grown up and living independently as well by now.

bundle · 18/04/2006 15:26

syd, it feels more uncomfortable than painful, a sort of tugging feeling and you're right the psychological side hits you pretty hard. i had amnios for both my pregnancies.

MeAndMyBoy · 18/04/2006 15:53

givemeachance, thank you for sharing your story. I feel sad that your parents felt that you should be involved in the decision they made, especially as it led to you feeling guilty. You certainly have no reason to feel guilty. It does bring so much into perspective - what is serious enough to consider terminating a pg? We are discussing amnio's and testing at the moment I am 11 weeks pg, am 35 and my SIL has very sever SN so feel that maybe it's something we need to consider. But we have already drawn a line at what we would consider serious enough - mainly down to the wonderful ladies on the SN board and their very moving stories of their fab children. I think a lot of people are in ignorance of what SN can actually mean and how much or little it would impact your family, certainly the case for me.

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