Edie_Rainbow_Baby

Mumsnet: This Is My Child | Mr Eli has Talipes and Benign Paroxysmal Torticollis.

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I have been looking, with interest, at some of the posts that have been published during the This Is My Child awareness campaign via Mumsnet. We live our life day-to-day as normal. Because THIS is our ‘normal’. Eli is our first born and we know no different. But I suppose, our story is different. I’ve not really highlighted Eli’s Talipes or (recently diagnosed) Benign Paroxysmal Torticollis on my blog before. I have mentioned in a few posts about his Talipes. But nothing in depth. So here it goes!

Everything stems back to when I was pregnant. I had a very tough first few weeks, after a bleed we were told that the pregnancy might not be viable at a 5 week early-pregnancy scan and told to return in 3 weeks time; where we saw the most amazing and incredibly tiny flickering – a heartbeat! PHEW!

We so looked forward to that 12 week scan. The sonographer was lovely, but seemed concerned. Eli was jumping ALL OVER, I thought she was just having difficulty measuring up dates because he wouldn’t keep still. She then turned the machines off and said she was sorry to tell us that our bundle of joy had a “nuchal fold measurement on the cusp of high”. The exact measurement was 3.5 mm. This was indeed the cusp before they offer you further investigation. We needed to know. We were informed that a high NT measurement could mean a multitude of conditions, including Down Syndrome. This was heartbreaking. This baby was so wanted – we needed to know what we were facing. We had ‘counselling’ and I had bloods taken. The nurse then called University College Hospital London and told us they had a referral for the the very next day. We were told we could have a more in-depth scan at the Fetal Medicine Unit; where we would also be offered the option of CVS – which would indeed confirm any anomalies, through a horrendously invasive procedure. After the lengthy scan with several specialists, we were advised that we could either go ahead with CVS there and then, or wait… It had been picked up that there was a lack of nasal bone; another marker for Down Syndrome. Our world shattered. HOW WOULD WE COPE?! We went ahead with the CVS there and then. It was like a whirlwind.

The procedure was horrible. Just horrible. I had soreness and tenderness for a few days after. Not to mention the constant worry and stress of the risk of miscarriage. It was a very very hard time for both of us, waiting for the results. 3 weeks passed and we received a letter confirming that everything was spot on with Eli. He didn’t have any of the common anomalies that CVS tests for.  We were over the moon to say the very least. PHEW!

But this was not the end of our hospital visits. To cut the (very!) long story short – we had a total of 9 scans. Because of the NT measurement, Eli’s heart, organs and growth was routinely monitored. He developed fantastically. At the 25 week scan, it was found our baby had a degree of Bilateral Talipes.  But it was “extremely mild”. PHEW! It was corrective. We were happy. In the grand scheme of things.

Fast forward to almost 42 weeks pregnant, I was just a HUGE pregnant ball; unable to move, pretty much. That little boy was so so squashed up inside my petite 5 ft nothing 1″ frame. I was eventually induced. Which, shock horror was just the WORST thing ever. (Incidentally, I would never recommend an induction. Just bloody wait till the baby wants to arrive!). After 30 hours of labour, Eli was pulled out of me in an emergency situation using Ventouse. He was out, safe, at long last. PHEW.

Or so we thought.

We both immediately looked at his feets. Yes, they turned in, but probably weren’t half as badly affected as we were imagining.

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Again, fast forward to 8 weeks old. We’d not been seen by a specialist. Not even had a referral. At Eli’s 8 week check the GP who was head of the surgery, told me that his feet would ‘correct themselves when he learns to walk’. I wasn’t happy with that. We’d been massaging, manipulating and exercising Eli’s feets since birth, but at about 8-10 weeks had hit that brick wall. They weren’t getting any better. With the encouragement from @BexandMic on Twitter, who’s beautiful son Hugo was also born with Talipes, I kicked off at the Health Visitor. I got a referral to see a Physio about his feet. At the very first appointment our lovely Physio, Jenny, pointed out that Eli’s head was tilted to the left. I couldn’t understand what she was referring to, he just couldn’t hold his head up yet… She explained it looked like he had something called Torticollis. Possibly from being so squashed up during pregnancy, possibly from the trauma of being pulled out so quickly. I was given exercises to do with his neck regularly, after a week, his head was straight! I still to this day can’t believe we didn’t notice it. Looking back at photos, his neck is completely to his shoulder on every single one. There was still tightness after a few sessions with the Physio and more manipulation on our part. We eventually saw our consultant, Mr Tuite at Broomfield Hospital on 31st October. Eli was almost 14 weeks old. Worryingly, most children with Talipes begin their treatment shortly after birth.

We were devastated when Mr Tuite said that Eli would in fact require plaster casts to begin the correction process. Mr Eli was pretty mobile at 14 weeks old! He was used to his bedtime routine and his bath. We knew the casts were for the best though. We had to do it. We were told Eli had really mild Talipes, again, so would require 2 weeks worth of casts…

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6 weeks later Eli was still in casts. It was incredibly tough.

Being the age Eli was, we got a lot of stares. You could just tell people must have thought he’d been dropped and had broken legs. When people asked what had happened, they didn’t understand. They made me feel like the story I was telling was a pack of lies. It was just a horrendous feeling. We did however have luck on our side, in the fact that it was Winter when Eli was in casts. It wasn’t hot, he would have been so much more uncomfortable if it was! He spent a lot of time in long socks and snow suits! In hindsight, I wish I’d been more confident with his casts. Embraced them more. Decorated them, even. The casts did not hinder Eli in any way, he was rolling over in them and they were SO heavy and awkward. He kicked his legs up and down and bashed the casts to bits! He was so brave – he didn’t sleep at night, but hey, he doesn’t now either!

The Torticollis would occur when Eli seemed to meet new milestones. It wasn’t constant. It was irregular. His neck tilted for around a week when he started rolling, sitting up and crawling. But also seemed to coincide with teething too. We continued to repeat the exercises and manipulations.

Mid-December 2012 and Eli went into Ponseti Boots and Bars 23 hours a day. He got an hour “free” where we gave him his bath and he had a kick about afterwards. This was a huge relief. We could get back to normality somewhat. We hadn’t even thought about the visual  impact the Boots and Bar contraption would have on other people. After our journey, we had just accepted what we had to go through.

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In the coming weeks, I had an array of comments and conversations about his B & B’s.

“They’re funky boots” “Thanks! They’re to straighten his feet” “ohh… I thought they were just fashion accessories! I’m so sorry. Didn’t realise your son was ill”. “He’s not ill?”

“Does he have broken legs?”

“Does he have broken hips?”

“Is that a contraption to stop him wriggling away from you?”

“Do they make him taller?” “WHAT?!”

 Etc. Etc. Etc.

We had a lot of nasty glances. A lot of nasty sniggers. I’m REALLY not thick-skinned at all. Like I say, I’d completely accepted that this was his treatment. It did not bother me. This was normal to us now – this was part of our every day lives! Until someone pointed his feet out, or made that eye contact, that’s when I’d think. Then it would upset me. But, I needed to get through that for him. It was in his very best interests. He wouldn’t be able to walk without it! Had we just been too blasé about the entire thing?!

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Eli wore his B & B’s for 23 hours a day, for 6 months. Most children wear them for 23 hours a day for just 3 months, then hours are dropped throughout the day until they eventually just wear them at night time. To our surprise, Eli went straight down to just nights at our next review. This was just insanely cool. It was just magical seeing him so free. His feet look PERFECT! We’re so so pleased. We’re also convinced though, that Eli struggles at night time because of his boots and bar. He’s free all day long, then come bedtime he’s confined. He can’t move with ease. It’s uncomfortable and heavy. He will sleep for 2-4 hours at a time. Then I will need to settle him. There has been nights where I have taken his bar or both his boots and bar off, and he’s slept soundly. I’m sacrificing my sleep so he can walk. Easy decision. I do worry it’s not good for him, the broken sleep. But what can I do?!

At 10 months, he started pulling himself up and cruising around his play pen. I can’t tell you how proud we both were. It was just so special; still is! SUPER PROUD PARENTS!

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Not long after Eli started standing up, there was an afternoon where Eli was particularly miserable. Anyone who knows Eli knows he is a jolly boy. Barely cries. He’s only ever grumpy in the night! He was super grizzly. I put it down to teething. Then he projectile vomited. His neck was tilted. He went floppy in my arms, the colour drained from usual his rosy cheeks, his eyes rolled back and he seemed to pass out. I was beside myself. Naturally. I rang my OH who calmed me down. I’ve never been so frightened, it was seriously scary. This had happened previously, but I wasn’t there. Another bout of sickness and drowsiness and I let Eli sleep. We then recalled another time when he projectile vomited (he was never a sicky baby so could recall these occasions clearly). Within in a few hours, his neck was back to its mid-line straight position. Without any manipulation. We worked out that they all coincided with his neck tilting. Could the Torticollis be causing this?

I took Eli to the doctors – who were, USELESS. He googled Torticollis and told me what Wikipedia says… He said he’d seen just one other case of this and to go back to the Physio if I was concerned. Hell yeah I was concerned. We didn’t know if it was underlining with something else. I went to Portugal for 4 days. Eli had another bout of the sickness and drowsiness with the Torticollis. Again, his neck had straightened up itself by the next morning. It was all definitely linked.

I went to the Physio again after my trip. She was lovely, she explained that the condition was Benign Paroxysmal Torticollis. This variation of Torticollis comes in waves, or ‘attacks’. The attacks can last anywhere from minutes, to hours, to days and is accompanied by vomiting, pallorataxia, agitation, infantile migraine, unsteadiness of gait upon learning to walk, general malaise and nystagmus. All sounded about right. The periods in which the child’s head is tilted and other symptoms appear can last anywhere from a few minutes to a few days, with a frequency of anywhere from two per year to two per month. Looking back at the frequency of the attacks, we’ve found they seem to happen at the beginning of the month – every month, so far. It seems to surround teething, more than milestones now.

So now we know.

But what to do about it. Well, we’ve been told my several doctors and the physio (as well as Google) that Benign Paroxysmal Torticollis is something that Eli will grow out of, probably by school age.

His most recent attack was on 6th August, his 1st birthday. His neck didn’t straighten up quickly this time though, it’s taken a good 10 days this time.

The additional care that Eli requires surrounds his Talipes and his Benign Paroxysmal Torticollis. We don’t know when he’ll be out of his boots and bar, could be at his next appointment (28th August), could be when he’s 3 or 4 or 5. We also worry about relapse; there’s also cases where the feet have been over-corrected so they point outwards. We also do not know when he will have another attack of Benign Paroxysmal Torticollis, or the severity. I have to carry dozens of muslins with me, just incase he projectile vomits. I often worry it’s just going to come out of nowhere. I also worry about when he goes to nursery – are there people who are going to be able to look after him if he has an attack? Luckily, at the minute, I can work from home. But he will need to go into nursery sooner rather than later, for him to be able to socialise with children his age, more than anything else.

We currently do not receive any help, support or funding. I do know of people who have been granted Disability Living Allowance for their children with Talipes.

I’d absolutely LOVE to hear from others who have experiences with Talipes or Benign Paroxysmal Torticollis. The latter being quite rare, so not heard or seen anyone else who has had a child with BPT.

Would we have had it any other way? Ideally, I’d love to have Eli without all the discomfort and challenges he’s faced – of course I would. But my goodness me, he’s a brave boy. He’s SUCH a character. And frankly, it’s made me and my OH better people. We’re stronger. We understand.

Worry, worry worry – isn’t that what all parents do?

MM.

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Mr Eli turns ONE!

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This was us, a little after 9:43pm on Monday 6th August 2012. I cannot believe our beautiful baby boy is now ONE! This year has just flown by. Mr Eli has been so so brave throughout all the challenges he’s faced – he’s the happiest little boy, with the cheekiest grin!

To celebrate his birthday yesterday, the three us of took a trip to Colchester Zoo. It was just brilliant. We had the BEST day! Colchester Zoo is just 45 minutes away from where we live; and after a recent trip to a farm we knew animals BIG animals would go down a treat with the birthday boy! He loved seeing the elephants, zebra’s, rhino’s and of course, all of the different types of tortoises! Can’t lie, OH and I enjoyed it thoroughly too. We made lots of “woah” and “ahh” noises throughout the day.

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Just a perfect way to spend the day reminiscing over Eli’s first year on the planet and how this bundle of joy has grown into such a handsome chap.

Happy very FIRST birthday Mr Eli. You’re our absolute world and we love you more than anything.

xxx

 

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We’re moving out of our first family home…

Eli packing

 

We’re sad (but oh so happy!) to be moving out of the first home we three have shared as a family. This move marks our 7th house for myself and OH, our second as a family. July has been ridiculously hectic, I don’t even know where to begin! But there will be more posts to follow our house move. We’re moving in the local area, just somewhere with more space for Mr Eli.

We’ve been concentrating on packing, in this sweltering 30c heat. As you can see, Eli puts my packing to shame. He’s really helped me out with closing those boxes up! Clever boy!

So so proud of Eli, he’s such a happy boy. And look how steady he is on his beautiful feets. Thanking you Mr Ponseti 🙂

MM.

PS – click on the image to view the InstaVideo. WordPress is being whack and doesn’t embed the video within the post, so it’s easier to just view it on Instagram itself.

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THANK YOU to John Lewis + iCandy.

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Mr Eli was so happy to be back in his iCandy Strawberry!

As I have previously documented, I’m a huge fan of iCandy. No-less because they’re a British brand with eye-catching, yet hardwaring products. It’s also very well documented that as a family, we’re HUGE fans of John Lewis. Again, another British brand with an amazing ethos for quality products and a company that prides itself in looking after its customers; and it’s partners (general staff!).

So, you can imagine my horror when one day I couldn’t remove the safety bar on my iCandy Strawberry pram. Eli was wearing his Ponseti Boots so it made it awkward to get him out. Eli had only been riding in the stroller/seat unit for about 5 weeks. So it was still pretty much brand new. I can’t say that this travel system was on the cheap side either; all in all it did cost nearly £900. BUT as I walk everywhere, the iCandy Strawberry was a definite investment – and I absolutely LOVE it.

As a Social Media wizard, my first point of call was to message the iCandy Facebook page. I left a comment on their wall and got a lovely response soon after. The iCandy Facebook assistant advised I contact John Lewis. So I did just that.

Unfortunately, you can’t call a store directly. You go through to the John Lewis central customer service centre, even if you have a direct number for the store you wish to contact. This however, is not a bother. The customer service advisors are so astute and just want to help you out. So jolly (but not annoyingly jolly!) and helpful they all are. This also means that all discussions are kept under a reference number so everything is kept organised and each advisor you speak to already know everything there is to know about the nature of your call.

I was advised that someone from the Stratford store would contact me with regards to having the seat unit fixed.

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Our iCandy Peach loan, soon after it arrived!

Someone called me from the Nursery department at Stratford about an hour later. After a few discussions it was decided that someone from the Stratford store would personally come to my home, on the train, with an iCandy Peach loan. Then they would take my iCandy Strawberry seat unit back to the store, where it would be sent away to be fixed. I cannot drive and now I’m working from home it makes it difficult to take a whole day off – plus it would mean paying for the cost of trains to and from Stratford, twice. I thought this was just incredible.

After the weekend sure enough, a lovely chap called Calvin from the Nursery department turned up, bang on time, with my iCandy Peach loan.

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Our replacement iCandy Strawberry seat unit came back in just over a week!

A week later, Calvin came back with my new iCandy Strawberry seat unit and collected the iCandy Peach loan.

Absolutely above and beyond. Just simply wonderful service from start to finish. I can’t think iCandy and especially, John Lewis enough. I’ve never ever heard of a retailer doing that for anyone. Retailers just aren’t like that these days. John Lewis have completely set the standard in retail customer service and they should be extremely proud of all who work for them! That kind of service is just off the scale. Unheard of. Exceptional.

THANK YOU JOHN LEWIS AND iCANDY! Just superb.

MM.

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What Eli Wore: Happy 9 month birthday!

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What Eli Wore today >>>

Top: Dinosaur Tee, Next, £6. Click here to purchase online.

Bottoms: Navy Shorts (pack of 2), Next, £11. Click here to purchase online.

Head: Hat (pack of 2 hats), Next, £GIFT.

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Today Mr Eli is 9 months old! He has officially now been out as long as he was in! Incredible. What a 9 months it has been. Completely full of up’s and down’s – and I wouldn’t change it for the world. Mr Eli is just an amazing human being – such a character. Our beautiful darling boy xxx

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To celebrate it being sunny, a bank holiday AND Eli’s 9 month birthday, we headed to Southend for the day. Got to make the most of that sunshine! Eli (with a little encouragement from us….) is a huge dinosaur fan. I’d been looking for some ‘cool’ dinosaur items of clothing for a while. But not really seen anything aside from realistic dinosaur graphics (which just look plain scary!) or overly-cartoonish style dinosaur graphics. But when I saw this tee from Next I practically POUNCED on it! It’s a great looking tee – cool dino print on front and back with a little chest pocket. Lovely stuff. Also have to mention these shorts! Because Eli will probably be wearing them a lot over the summer! They’re a 2-pack from Next, £11. Come in Navy and a Cargo-Brown colourway. They’re extremely hardwaring, wash great, wicked quality and made using a heavy cotton so they can be dressed up (with a shirt) or dressed down, like today.

Next have some really good clothing this season for your little man. I tend to go for mini-Daddy style clothing, rather than cute kids clothing. So if you’re after the same kind of thing, give Next a whirl. So so good. Great prices too!

MM.

 

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Oh hello, it’s been a while…

Merry Christmas and Happy New Year!

I know, I know. It’s been a canny while. Life has been pretty hectic to say the very least.

SO MUCH has happened since I last properly updated.

– Mr Eli has been in and out of plaster casts for his Talipes treatment. He’s currently in full time B & B (Boots and Bars). I’ll do a proper update on this too.

– We’ve had our first Christmas together, which was AMAZING.

– New Year came and went without a hitch.

– Started feeding Eli proper, actual, proper food! Which he LOVES.

– We’ve been here, there and everywhere visiting friends and family.

– I finally overcome some very difficult decisions and feel a ton has been lifted from my shoulders… albeit, it has been replaced with a wee bit of stress. But I’ll reveal all later! It’s all a bit hush hush right now.

– I’ve FINALLY started driving lessons! It’s only taken me 10 years.

Think that’s all for now. Will catch up again VERY soon!

MM.

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Mr Eli has Talipes…What happened next?

Just hours after Eli was born, 6th August 2012.

It’s just dawned on me that I have failed to write about Eli’s Talipes! I did blog about it when I was pregnant as it was found when I was having additional scans at UCLH, you can see the original post here: Hospital Update: Baby Boy bump has (mild) Bilateral Talipes. And I mentioned it in the 4 week update I did, here: An Eli Update: 4 Weeks Young. But I haven’t updated my blog with the developments since…

So from the top, it was found during an additional scan at UCLH that ‘baby boy bump’ had mild Bilateral Talipes. As the weeks progressed and I got bigger,  it meant that ‘baby boy bump’ got more and more squashed up inside me. This was the cause for Eli’s Talipes; it’s “positional” due to him literally being too big for me!

As you can see, from the first picture above (taken just a few hours after Eli was born), the Talipes looks really mild. But it turns out Eli was quite lethargic after my traumatic labour and birth. It wasn’t until he was home that we noticed how much he pulled his feet inwards (picture below).

This photo looks distorted, must have been a strange angle! Eli is 4 days old.

We were seen by a Paediatrician just before we left Broomfield Hospital and we were told that Eli would need his hips X-rayed and of course, Physio. I was told to expect both appointments within a few weeks.

After 3 weeks, I spoke to my Health Visitor who advised to wait one more week and then chase. I chased and chased and chased. I was pushed from pillar to post between departments. I couldn’t believe how badly organised everything was. (Hence why I haven’t actually written about this until now!). It was an absolute shambles. I finally received an appointment for Eli to have his hips scanned when he was 7 weeks old. During the scan I was told his hips were absolutely fine! (PHEW!) And again, that his feet were an isolated case due to him being so crammed in (Sorry boy).

I was STILL yet to receive an appointment for his Physio at this point. But as we have common sense, from birth, we had been massaging Eli’s feet ourselves with exercises we found on the internetz.

8 weeks old, after his first set of immunisations.

-You can see Eli’s left foot is much straight, but his right is still pulling inwards.

We saw a marked improvement with this – until about 9 weeks, when it just seemed to not get any better. It felt like we’d hit a brick wall. I finally had my appointment with the Physio when Eli turned 10 weeks. I’d like to point out at this is appalling. It took 10 weeks to finally see someone and the Physiotherapist, although absolutely lovely, gave me the exact same exercises to do. She said that it’s the muscles and tendons on the insides of both feet that are tight; causing Eli to pull his feet inwards. She suggested that Eli might need plaster casts, and in her opinion, it would only be for a week. I already had another appointment organised with a leading Talipes Consultant at Broomfield for when Eli was 12 weeks old. Again, this is terrible – we should have had Eli seen by a Consultant WAY BEFORE he got to 3 months old. I’m extremely unhappy about how long it’s taken and the awful communication, or lack thereof, between departments.

10 weeks old feets 🙂 

Last week we finally saw the Consultant at Broomfield. He looked at Eli’s legs, hips, spine, neck and feet. Which we didn’t expect, but was really reassuring. He agreed that Eli has Positional Talipes and has advised a course of plaster cast treatments. The casts will go from his foot and up his thigh – to avoid him kicking the pot off! When the Consultant left I spoke with the Senior Nurse (who organised our first appointment for THIS week). The Nurse advised that Eli will wear the casts for up to a fortnight at a time and will then need to wear special boots inbetween plaster cast treatment, the Consultant did not mention this, so I’ll see on Wednesday of this week what the definite course of treatment will actually entail. This sounds like Eli would be undergoing the Ponseti Method, but like I say, we’ll find out this week.

I am SO SO pleased that our beautiful baby boy is finally getting his little feets sorted out. Better late than never I suppose.

I’d like to hear from you. Has your little one undergone treatment for Talipes? What was your experience? Can you offer any advice or tips?

MM.

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An Eli update: 4 weeks young.

Weight at 4 weeks: 9lb

Length at 4 weeks: 53cm

Yesterday marked Mr Eli’s 4 week birthday. I actually cannot believe how quickly these first 4 weeks have flown by! I also can’t believe how quickly our little boy is changing too! He’s so strong and curious about the world; he can hold and move his head so well, already!

When your newborn, is newborn, their hearing is checked in the hospital. Unfortunately, due to my quick delivery, Eli had A LOT of fluid/blood stuck in his ears for a few days after the birth, which meant that the hearing test failed to work and would be repeated. We weren’t concerned because Eli had proven he could hear very well! From as soon as we got him through the front door he looked for where sounds were coming from and would jump if there was a bang or a clap etc. So yesterday I took him for the repeat hearing test… we got to go on a big train!

Mr Eli on the big train!

Granted, we literally went one stop on the big train – but still! He was as good as gold all the way there (even when Mummy got lost on a building site!). Then as soon as we walked into the testing room, Mr Tetch arrived! Which meant that it was difficult to get a clear reading. Breast feeding commenced and a clear response was found straight away. So that’s done with 🙂

We’re still awaiting an appointment for Physio for Eli’s mild Talipes however. I’ve been chasing the hospital on a daily basis but am getting nowhere. It’s a good job we have common sense and have been massaging his feet ourselves (which is definitely working, we can see a difference already).

 

MM.

 

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Hospital Update: Meeting the Consultant and measuring 34 weeks at 28 weeks.

My favourite image of our Baby Boy so far! Taken at 20 weeks, UCLH. 20th March 2012.

Yesterday morning we drove up to Broomfield Hospital for another appointment with our Consultant; to discuss the findings from our last scan –The Bilateral Talipes. But our actual consultant was stuck on the M25 (of course), so we saw someone else and had to go through the whole rigmarole of explaining everything that’s happened in this rollercoaster of a pregnancy!

Fast forward half an hour and I’m on the couch being measured up with a tape measure again. At my Midwife appointment, less than a week ago, my bump was measuring up at 30cm, so 30 weeks – Weekly Update: 28 weeks. So had expected it to be about the same.The two Doctors measured me again… I was measuring 34cm, so one would assume, 34 weeks! UH OH.

I was referred for an emergency scan to check out baby boy’s measurements properly, along with an index of my amniotic fluid. Had to sit around the hospital for 3 hours until the scan. MASSIVE YAWN.

Had the scan and everything was FINE. He’s measuring up at 29 weeks (of which I am 29 weeks tomorrow). He weighs about 2 and a half pounds. He couldn’t be more spot on measurements wise, he’s spot on all the ‘average measurement’ lines on the scan graph. Which is great!

Also, my amniotic fluid is showing up at 6cm at the deepest point, which again, is absolutely normal! So everything is great. I just have a lot of my own water retention and bloating..possibly because I drink far too much water. What can I say? I’m a thirsty girl!

Additionally, the Sonographer also said that we no longer need to go back to have a scan at 32 weeks. She’s more than happy with the progress of everything and doesn’t see why we should have to go back to the hospital to review baby boy’s Talipes. Which is also fine by us! We’re over the moon! But at the same time, I’m also a little bit sad that we won’t be seeing our baby boy for a little while… in fact, the next time we see him will be when he’s ARRIVED! Which to be honest, is also a little bit scary! It’s all very very very REAL now. EXCITED.

So the moral of this story is, don’t believe the measurements! It was never going to be an exact science, measuring your bump – who thought it would be?!

MM.

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Our little (Converse) family.

Couldn’t resist doing a couple of snaps of these! Daddy, Mummy and Baby Converse! TOO CUTE.

My sister surprised me this week at work by posting the Baby Converse direct to me… So of, course I had to get an obligatory shot of our little (Converse) family before Baby Boy arrives! We’ll have to get another shot afterwards, with us all wearing our respective Hi-Tops!

I actually cannot wait to get our Baby Boy in these… they are 3-6 months, so hopefully, if his Talipes has progressed, we’ll have him fixed before he’s 6 months old!

Converse ‘First Star‘ Kids Trainers, £21.99. Click here to purchase from Office.co.uk

MM.