CVS: The Full Results.

Thursday 2nd February: The full results came back.

I had anxiously waited all week for that ‘BLOCKED’ number to call me again. It got to 4pm every day and I felt physically sick. I was shaky, dizzy and unable to concentrate at work. I was going to give it until Friday 3rd February at lunchtime, and then I was going to call UCLH to chase up the results. I couldn’t bear another weekend not knowing.

We got home from another tiring day at work, I felt withdrawn and exhausted and drained at the fact I hadn’t had that phone call, again.

There was a few pieces of post on the doormat… including one postmarked ‘London’, the address was handwritten. I just KNEW these were the results. I felt that pang of sickness and dizziness again.

We sat down together on the sofa as I struggled to open the envelope. I quickly glanced over the letter just looking for the words ‘normal’ and ‘positive’ and ‘clear’. The letter was a generic, photocopied letter.

But we saw the words we desperately wanted.

“We are writing to inform you that the results from your CVS demonstrate that your baby has a normal chromosome pattern“.

We were overjoyed! The letter was post-marked as 30th January, so the results took less than the two weeks to actually come back. Shame the hospital couldn’t call me to tell me directly – it would have saved a whole lot of agony. But still, we got the results we hoped for!

The letter also stated that we could call the FMU department to find out the sex of our baby. We we desperate to find out! So I called first thing the next day and they called back to tell me that we were having a LITTLE BABY BOY!! Absolutely ecstatic. We weren’t hoping for a boy or a girl specifically, but were beyond surprised to find out we’re having a boy! My partner is the last male on his families side, so we’ll be carrying his family name on – which is a wonderful bonus! We’re still in shock – but it’s so lovely to be able to bond with him properly now. Our little boy 🙂 Most people don’t get to find out the sex of their baby until the 20 week scan and even then, the scan isn’t 100% accurate! So we felt a little bit smug knowing that we’re having a boy, and that it 100% definitely is a boy! 😀

The next stage was an Echocardiogram (detailed Fetal heart scan) at 16 weeks – scheduled for Tuesday 14th February. Aptly, on Valentines Day.

MM.

CVS: The Rapid Result.

Wednesday 18th January: The Rapid Result came back.

I was laid on the sofa with the quilt, again, running through every single scenario possible. We were told that we’d get the rapid result back within 3 working days, and that an FMU midwife would call after 5pm. We anticipated that we’d get the phone call on Friday 20th January. My mobile started ringing at around 5pm. The number was ‘BLOCKED’. I knew it had to be them. I sat myself up and prepared myself.

The FMU midwife asked me to confirm my name and date of birth and then said the words we’d only hoped for, the results were NORMAL. That meant that there were no abnormalities with regards to Down Syndrome, Edwards Syndrome or Pateau Syndrome.

I rang my partner first and we both cried. I then rang my parents and close family – then my best friend. We all could breathe a sign of relief and relax, a little bit, until the final report came through…

This was the most agonising 2 week wait of our entire lives.

MM.

Referral to UCLH for the CVS procedure.

Tuesday 17th January 2012: Appointment at UCLH for detailed scan and CVS procedure.

With barely a wink of sleep between us, we arrived at the Fetal Medicine Unit at 9am for our 9:15am appointment. We were taken a for full scan which lasted around 45 minutes. There were two specialists and a FMU Midwife present, along with a student who was observing. The specialist doctor who was performing the scan said that there was a lack of nasal bone visibility, which also carried through as a ‘soft marker’.

We were taken into a family room where we could discuss our options… and we were then joined by an FMU Midwife who went through the basic pro’s and con’s of the procedure and the impending results that would follow.

I signed the consent forms and was taken back through to the specialist room where the procedure would take place.

The doctor and an additional Midwife scrubbed up and I was given two injections of local anaesthetic directly into my tummy, on the left hand side. The injections were the easy bit…

After around 5 minutes the anaesthetic had taken hold and the doctor proceeded to take the first of the placenta samples, while the FMU midwife constantly scanned my tummy. The procedure was uncomfortable and felt like tugging. I winced quite a fair bit and squeezed on my partners hand so tightly! I just kept looking at him and both he and all the staff present reassured me throughout. I felt in safe hands, with the best in the business!

The second biopsy was taken and I breathed a sigh of relief. The FMU midwife showed us our precious little babbit on the screen again to reassure us of his movements again.

I was then taken, slowly, into a recovery ward where one of the FMU midwife’s who had been present joined us to explain that that procedure had collected two successful samples that would be sent away asap. We were to get the ‘rapid result’ back within 3 days. The rapid result checks for Down Syndrome, Edwards Syndrome and Pateau Syndrome. The rest of the results would follow in around 3 weeks with a detailed report on rarer chromosomal abnormalities.

After recovering for a further 25 minutes or so, we were free to go home. My partner took me home and I tried to sleep on the sofa all day. I was exceptionally emotional and quite sore. I was advised that I may have period-type pains, some bleeding and soreness for a few days. I could not help but run over every single result and scenario in my head… and again, barely slept a wink that night.

MM.

 

MASSIVE catch up! The 12 week scan and what followed…

I can only apologise for not writing on this blog more frequently. But when you read my following posts (to come!) you’ll completely understand why it’s been a difficult couple of weeks.

I’m going to be magic and go back in time and catch up on EVERYTHING that has happened since the beginning of January. Circumstances have occurred since our 12 week scan that we hadn’t even read/heard about, nevermind had the time to contemplate. BUT, we’re through the other side now and, certain that everything will continue on the successful streak that we’re currently embarking on!

So let’s go back to the beginning then…

Monday 16th January 2012: 8:45am – The 12 Week Scan.

We eagerly waited to be called into the Scanning room  at Broomfield Hospital, Chelmsford, with a overly full bladder (ouch!). We were briefed by a Midwife regarding the 12 week optional screening… we had already agreed between us that we wanted to go ahead with the screening. The screening that day would include a blood test and further look at several measurements of our little babbit during the scan.

We were beyond surprised to see how big our little babbit was! He was so lively too – bouncing all over, waving and dancing!

During the scan the sonographer looks at the nuchal fold and gives a measurement based on the visible fluid.  Also known as the Nuchal Translucency measurement, this screening looks at the thickness of soft tissues at the nape of neck of the foetus. It was revealed that the Nuchal Translucency measurement for us, was on the cusp of the borderline between normal and ‘high’. The result measured at 3.5 mm. This is the actual borderline. We just couldn’t believe it. Albeit, it wasn’t as high as some peoples’ measurements that we’d heard of – some as high as 10 mm.

From then on, we were whisked off to a counselling room where another Midwife briefed us on our options.

We decided that we wanted further investigation and while I was having bloods taken, a referred to the Fetal Medicine Unit at University College London Hospital (UCLH) was set up . Because of the sensitivity of time, the referral was organised for the very next day. The appointment at UCLH would include a detailed scan, councelling and the invasive Chronic Villus Sampling (CVS) procedure based on the results of the scan and our consent. CVS would be able to tell us if there were any genetic/chromosomal abnormalities.

 

Here is our precious little babbit – aged 12+3 weeks. Due date measured as 27th July 2012 – the day the Olympics begin!

We went straight back to work following the scan and revelations. I spoke to my boss, who was beyond understanding. He agreed to giving me the rest of the week off owing the invasive nature of CVS and the risks attached (2% risk of miscarrying).

Once we got home, we looked online to try and fathom what actually happens after CVS and other peoples’ experiences. We found lots of forum posts and blog posts on CVS and the procedure, but failed to find details on what happened post-CVS, the results and what it means. Hence, why these following blog posts are going to be a little bit more detailed than my usual posts. We just wanted to share our experience with everyone!

MM.