Showing posts with label #baby. Show all posts
Showing posts with label #baby. Show all posts

Thursday, 1 October 2015

Surviving motherhood with a chronic illness




Being a mum is one of the most greatest gifts in life and is full of joy  but it comes with its fair share of challenges, but when you have a chronic illness, parenting has a whole new set of challenges and worries, along with new highs and lows, not just yours but there's, repeating the word no a million times, dealing with lost shoes, socks and dummy's, the never ending chores and washing pile, the temper tantrums at bedtime and when they cant get there own way, can take its toll mentally and physically, but how do you look after a baby when you can barely look after yourself some days, and just want to sleep the day away, how can you juggle  doctor, and hospital appointments and a baby all at the same time. A few times I had been called superwoman for doing it all myself especially after my ablation, being to stubborn to ask for help and support or simply because I feel guilty leaving Kian , but if there's anything I have learnt you have to be well enough yourself to look after them, like on a plane the cabin crew use the ' fit your own masks before helping others' and that's such a big thing when it comes to being a parent with a chronic illness, and its took me a long time to actually find a balance with the whole spoon theory and being a mum, you can't just take a nap and gain some spoons back your on the job 24/7, no coffee breaks except for a good nights sleep if your lucky and its such a true saying of needing eyes on the back of your head.

 When I was pregnant, everyone would go on about the labour and  birth and I spent my whole pregnancy absolutely terrified, preparing for what was about to come, from the excruciating pain to becoming a shell of my former self , but labour is the easiest part you can take all the drugs to help ease the pain of labour and having your baby like everyone says you forget the pain, crying because your actually happy is something you can't control the first time you set eyes on the bundle of joy you carried and felt wriggle inside you for the 9 months , but nobody warns you or prepares you for how difficult and challenging being a mum is, there's no drugs for that and being a sick mummy means the road is even more bumpy but its all about learning and doing things a little different.




I wanted to share some of the things I do and that's helped me with my heart problems, It is not a choice to be a parent  living with chronic problem, You did not choose to be chronically ill, so get rid of any guilt that is eating away at you, you wont always be the best parent, partner or friend but nobody is  perfect, Remind those around you, especially the children in your life, that you love them and that you are there for them. It may not be in the ways that you had originally planned or hoped, but it is no less valuable or meaningful, a cuddle or reading a story wiping the grazed knees, saying I love you and above all just being there when they need you is the most powerful thing you can do as a mum Take each day as it comes and let the expectations of what you ‘should’ be doing fall by the wayside. Try to live in the present and find the balance in your life, focusing on all the good things. This attitude will  help you go a long way towards maintaining a positive outlook to being a mum with a chronic condition.

Its ok to ask for help, it doesn't make you a failure



I was never one to ask or admit I needed help and always tried to do it all on my own, the fear that it made me a bad parent the thought of failing Kian but not asking for help just made my health worse
I was exhausted mentally and physically which all just made my heart ten times worse which just meant I ended up in hospital or to unwell to look after Kian at all, and it wasn't nice been stuck in hospital away from him for a few days, were if I had just accepted or ask for help in the first place I wouldn't have became so exhausted So I guess what am trying to say is rule number 1 it doesn't make you a bad person asking for help if you need it, everyone needs  help and by asking for help its helping you which in turn is also helping out the little one, and something I learned is nobody judges or thinks any less of you by asking for a helping hand.

Find the balance




Parenthood and chronic illness becomes a huge part of your identity and both can fight for control over your whole life, your time, energy, and some days, sanity, and its frustrating, Kian only being a baby he doesn't understand so I learned I can't blame him when I do want or need an extra 5 minutes in bed or a rest and just leaning to adapt helps, I found taking him along to a local play cafe were its all mats and baby proofed I could let him crawl about  and play and I could sit on the comfy  sofa with a cup of tea and just switch off for that 5 seconds without the worry of him hurting himself, and the added bonus there's other children there which meant a cup of tea without a baby grabbing onto my leg demanding me to play so always make sure that you take care of your own personal well being, as well as caring for others these are all important to finding the balance.



Get the extra support that's out there

I was amazed at how much support is out there for mums and dads who do need extra support wither it be down to an illness being a single parent or even just finding the whole thing difficult there's so much out there from places to go and speak to someone, wither it be lacking confidence to go out and do things, or just to talk to a friendly face, there is support were you wouldn't be judged health visitors and your own doctor can guide you in the right direction, even reaching out to other people via support groups who are going through similar struggles  can provide the emotional support needed to get through the toughest of days and be a great source of encouragement and advice, and its a great way to meet new understanding friends.


Know your limits, don't over do it

If you are having a bad day or you feel like your running low on spoons order a  take away for dinner ignore the house work  it can all wait. Your health and well-being are more important than a dirty-dish-filled sink or a messy floors,  don't focus on the negatives this is understandably more easily said than done, but understand that you are not your illness. The ability to find some good in even the smallest things can change your life on a daily basis, its amazing how changing your mind set can help mentally as well as physically Rome wasn't built in a day and if you start looking at life from that view you will realise you will get there eventually just knowing your limits and boundaries.

Limit children to one baby proof room



Limiting small kids to one room and baby proofing it can make things manageable when your having a bad day, I found getting down on the floor to there level and hunting and moving anything and everything that could become broken or go in small mouths and putting a stair gate on the door, I didn't bother with fire guards instead blocked the fire place and TV with the coffee table and large toys that stopped Kian been able to get through, yeah my living room looks so untidy with toys and things everywhere but it makes it great for a day when you need to lie back on the sofa and you can still keep little ones in your line of vision and buy using large toys and things is also saving the cost, you will feel like superwoman not only managing to lie down to feel better but also managing to look after the little one to.

Learn to put your needs first

I know this sounds such an awful thing to say and obviously being a parent your child is your number 1 priority but be assured, it is a good step in achieving optimum levels of health, both physically and mentally, You cannot be your best for others if you are not your best for yourself. Find time for a quick bath, listing to some music just doing anything that you enjoy doing yourself wither it be when the kids are asleep or letting the hubby take over for a night putting your needs first will improve your health its amazing what recharging your batteries can do.

Kids get bored at appointments




Having a chronic condition means the endless trips to appointments, its no fun getting an ecg done and having a screaming bored baby in the pram, I always try to get someone to look after Kian which is the easiest thing to do but isn't always possible and on many occasions I have been trying to listen and discuss my heath with doctors and Kians been crawling round the room, sometimes I have had to feed him a bottle just to get him to sit and sometimes I have even found myself apologising to doctors for Kian's behaviour but there kids they get bored hospitals are warm and stuffy so who can blame them, one tip I always found was giving Kian a new toy to play with it doesn't have to be anything expensive, and its normally the small silly things they like the best like Kian's favourite is spoons or anything that makes noise and that helps see him through the appointment, there's always the bonus that everyone is aways so friendly and chats away when you have children with you, and on some occasions Kian has even got some penny's for his piggy bank, so I suppose it isn't all bad if you do have to take them with you.

Don't be afraid to go to groups.





This was one I wish I had done sooner with Kian, just because you hear the word toddler groups etc you think running around 3 year old's but actually there's something out there for all ages and by getting out meeting new mums and children is such a good way to discuss parenting its also good for the kids to meet other children and learn to share etc from a young age and I found also kept me sane because it can be a long boring day when you do feel well enough to venture, I found everyone was so friendly at groups and if I was left sitting alone the teacher of the group would always come and make  chat anyway and by going to one group you learn of others and its great fun playing with messy play and getting involved it kills a few hours and keeps the kids amused,  places like the library, museum and park are also good and totally free or the good old favourite a walk, all the groups you do pay for are mostly small donations so one week if you are having a bad day it doesn't matter if you don't go.








Always remember the struggle won't be forever,  so don't ever let a chronic condition stop you having the greatest gift in life and that is having someone call you mum.



                                                                   
                                                           The last time


From the moment, you hold your baby in your arms, you will never be the same, you might long for the person you were before when you had freedom and time and nothing in particular to worry about.

You will know tiredness like you never knew it before and days will run into days that are exactly the same full of feedings and burping, crying and nappy changes, whining and fighting naps or lack of naps it might seem like a never ending cycle

but don't forget there is time for everything, there will come a time when you will feed your baby for the very last time. They will fall asleep on you after a long day and will be the last time you ever hold your sleeping child.

One day you will carry them on your hip then set them down and never pick them up that way again. You will scrub their hair in the bath one night and from that day on they will want to bath alone. They will hold your hand to cross the road then never reach out for it again, they will creep into your room at midnight for cuddles and it will be the last time you ever wake to this.

One afternoon you will sing the wheels on the bus and do all the actions then never sing them that song again, they will kiss you goodbye at the school gate the next day they will ask to walk to the gate alone. You will read a final bedtime story and wipe your last dirty face. They will run to you with arms raised for the very last time.

The thing is you won't even know its the last time until there are no more times, and even then it will take you a while to realise, so while you are living in these times, always remember there are only so many of them and when there gone, you will yearn for just one more day of them one last time.



                                                               Love and hugs

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Sunday, 14 June 2015

What living with an invisible/chronic illness is really like







Movies like my sisters keeper, the fault in the stars  all have a begging a middle and an end maybe not a happy ending but an end were you close the book or turn off the movie and if your like me in floods of tears but you feel satisfied that there's an ending , but my health hasn't had a happy ending . And that's what having a chronic illness is like there's not a happy ending the ablations on my heart have never worked .. And the average person doesn't know what having a chronic illness is like, what it's really like to be sick, to be in a constant battle with what you physically want to do but your physically unable to no matter how hard you try you can't feel better because you can't escape your own body so I thought I would share that with you because being sick isn't glamorous like the movies make out , I mean what's glamorous about being in hospital gowns covered in constant bruises because of all the needles or how even combing your hair is a mission so half the time you don't comb it unless it's to try and feel better or of course take a selfie.

Having the flu for example or the cold you feel awful but after a few days you start to feel better but having a chronic invisible illness isn't like that they few days turn to weeks which turn to months and for me even years, it doesn't go away yes you have good days which are very few and far between and you treasure they good days and appreciate them but the symptoms you feel never go away.

The fatigue and tiredness you experience everyday you can't just go to bed and sleep at night and wake up feel refreshed, I can't even remember what feeling refreshed feels like.Its a daily struggle but you just have to get on with it, your body and mind simply go into auto pilot and you just have to find a way to cope with it you can't just sleep it off.

 I can take tablets everyday just to stop me fainting, feeling dizzy and to stop my heart from racing but even taking tablets it doesn't go away or cure it, it manages the symptoms, but even taking the tablets they don't stop the fatigue and tiredness in fact the tablets make the tiredness worse because you have no choice because feeling exhausted is far better than fainting and being physically unable to get up in the morning, and there's more awful side effects with the tablets like the vision problems you experience where bright flashing lights flicker in your eyes or when they slow your heart down to much the chest pain breathlessness but again you just get used to it because you have to.

All the appointments and check ups you have to go to, the hospital and doctors becomes your second home, were every doctor at the surgery knows you, when you phone up or go to the reception desk they greet you and know your name without you even opening your mouth, and you know your there so much when they start to ask about your husband etc, even going to accident and emergency they recognise you because your there so much, part of you feels embarrassed when you can spot and point out your huge folder of notes that is bursting at the rim because of all your admissions.

Being scared of needles or been frightened of tests just doesn't exist because your so used to it its like having a cup of tea you just drink it and having a chronic illness your just used to it, the pain of the needle you barely notice it now because its like you  become immune to the pain you know you don't have a choice and its just got to be done, you feel no emotion to any of it but having a chronic illness its not as simple like others,just putting in the needle and taking some blood, because your veins just don't exist anymore yeah you have them but they are thin and frail from all the times they have took blood and if they even attempt they just collapse, so it becomes a task and you get used to millions of doctors trying and failing and it takes ten times longer and in the end give up or if its a must and you do need fluids or drugs,they have to find an ultra sound machine so they can scan you all over just to hunt and find a decent vein.

Things people say to you can be upsetting and frustrating and can even make you angry because they just don't get it its like they try to be helpful but there words can be hurtful and I wanted to share some of things people have said to me and if your reading this and don't suffer a chronic condition you might just think about what your saying and how it can affect people.


When someone says give me a phone or let's meet up when you feel better 

Chronic means chronic it's persistent its long term, it's not like a cold or the flu it doesn't just go away it's long lasting. So please just don't say it yes I will try to meet but when I do meet I am still sick I am either having a good day or I am feeling complete pants but am just trying to get on with it .

Your to young to be sick 

  I didn't ask to be sick nor did I want to be sick, what age is it acceptable to become sick ? If I reach                                                              60 does that make it ok ?

You don't look sick 

What does sick look like ? You don't say to someone going through a divorce ohh you like like a divorce because it doesn't look like what's happening to you .. If my chest thudded and vibrated and I looked tachycardia  or looked like high blood pressure would you stop saying it ?



just get on with it

Most days I am doing exactly that I am just getting on with it despite the way I feel getting on with symptoms if I didn't I wouldn't even get up in the morning I wouldn't eat shower or be a mum there's a difference between getting on with it slapping a smile on doing normal things than when your generally having a very bad day that your physically unable to do those things but you don't want to be sick so when you are in bed or  cancelling things its not because you don't want to do those things its because you can't ... and it does hurt to cancel plans or nice things and you spend your day lying in bed feeling awful but also feeling miserable because you did want to do those things.

It must be nice getting lots of time off from work 

Yeah its nice to have a holiday but its a totally different story when your physically unable to work even though you want to and is a totally different story , I mean who wants to stop getting paid because there off so much believe me its not nice been off work and spending days been stuck in bed or hospital just trying to distract yourself from the way your feeling, having to explain why your constantly off sick and why your not getting better, I would trade my illness with anyone who wants that lifestyle of feeling awful and been stuck in bed all day.

what if you exercised more ?

yeah if you exercise and are fit and healthy that helps lower your heart, but having ist nothing lowers your heart, yes doctors tell you to exercise and do what you can but having a normal resting heart rate over 100bpm sometimes your just not able to, and even when you exercise which for me is something simple like walking you have to watch your heart doesn't speed up to much or that just makes you even more sick and could result in fainting which just knocks you further away from good health and were you want to be.

 Its in your head/anxiety 

If I had a pound for everytime I heard this before I got diagnosed with ist my purse would be heavy and I would be a rich, its like when you physically look healthy its just assumed its mental yes anxiety and stress can make ist worse but who doesn't get frightened or scared of passing out alone but you do have a physical illness and ist before it became a known condition patients going to the doctors with fast heart rates and fainting were told 'its in your head' but research showed people with sinus node modifications didn't have fast heart rates anymore so before you say this to someone with a condition just stop and think its not helping and if anything causes you to feel more fed up, stressed and miserable.



I know someone with the same condition and they manage

Everyone reacts different to an illness, like how everyone reacts different with a cold, just because someone manages more than others I managed my whole life having a fast heart rate but it didn't bother me and led a normal life until 3 years ago this really doesn't help or make you feel better so just please don't say it its like people try to encourage you but it doesn't you can't help it, some people with ist can't even shower without fainting were as others can run etc and manage.

So as the saying goes stick and stones may break my bones names will never harm me... words do hurt its amazing how simple little things can make all the difference so I thought I would share these with you to a simple act of kindness does really go a long way.


Can I come over ?

sometimes leaving the house is to much so someone saying can they come over makes all the difference its nice to get company but doesn't use up your energy or spoons it shows they want to spend time with you but understand you cant go out.

Sending a message

Its always nice to know that someone is thinking about you, if you have been off work for a while and generally haven't had any company I mean out of sight out of mind?   it just makes your day when you know people are there for you and thinking about you.



I understand

Saying this to someone stops them from feeling guilty or a burden if they have cancelled plans, I mean I always feel awful about cancelling and I always leave it last minute as I always hope I feel better letting them know your not mad just helps the guilt and makes them feel better and makes you more likely to make plans again because you wont be afraid of losing them as a friend

Hug

Sometimes you don't even have to do anything just a hug goes a long way and it really helps knowing someone is supporting you and listening when I was getting induced with my little boy and it kept failing meeting up with my community midwife and her just hugging me as I walked into the room lifted a huge weight from my shoulders and it did really made all the difference, even an extra cup of tea from the midwife's at the hospital just made me feel that whole lot more positive about things.




I believe you

This is the most wonderful and powerful thing you can say to someone with a chronic condition seeing is believing when you look healthy its like people doubt you having someone believe you is the best feeling in the world and gains trust and shows a true friendship and is the best thing you can say to someone with a chronic condition.


 I hope everything I explained in this blog post helps people understand what having a chronic condition is like my next ablation is on Tuesday and as I have explained before this might not cure me but will ease my symptoms and help me with everyday life at the moment I just feel in a constant battle with things I want to do but physically am unable to do and above all I just want to be a mummy to Kian and live life to the full even with a chronic illness these simple things make all the difference, we are just back from sunny palma nova were I enjoyed the sun sea and spending time with my boys it was so nice to get away and be a family and to actually feel good.









Kian has now reached 29 weeks and is nearly 7 months and at this age things are getting easier its so rewarding now he communicates in his own little way by always smiling at my voice turning round to look for me when I speak and on Tuesday its going to leave a huge empty space in my heart been at the hospital without him, he's the whole reason I want to recover quick as I am frightened of missing things, I would hate for someone else to hear his first words or see him sit up I just want that person to be me.


29 weeks today sits up on his own but still falls over if he reaches for things is now sleeping in his own room rolling about more but prefers to stand or bum shuffle if u shout his name he turns to look at you a lazy eater and will just swallow things in one go 🙈 now naps more during the day and doesn't fight his sleep also likes to lie on his side to go to sleep always so happy and smiling






















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Thursday, 29 January 2015

My baby boy at 10 weeks old

To my little Monster Kian






Your now nearly a quarter of a year old, your one of the happiest babies I know constantly smiling and laughing at anything and everything, you love to smile at your reflection in the mirror. I put you down in your big cot with the mobile and you loved it, the rabbits spin and play music you get so excited watching it your legs start to kick you wave your hands about and your eyes follow it you start smiling and screeching at it you always get so excited.






You also have a thing for your hands dad laughs because I call you a little magician but you also clasp them together and play with them and they also always end up in the mouth your necks getting stronger and are managing to hold it up. You keep giving me a fright every morning I wake up as you some how always manage to kick all the way to the top of your little carry cot and pull your shawl over your face and just laugh and smile when I try to pull it down and tuck it in. Your such an amazing sleeper going down between half 9 -10 and sleeping right through to half 6 -7.




When I took you for your jags the other week you screamed I think you were the loudest in the doctors but when I sat feeding you in the waiting room you started smiling and laughing at the other babies. Your slowly starting to grow out of your newborn clothes and making your way into 3 month outfits you were 9lb 3oz at 7 weeks old  I can't believe how quickly you are growing up we are starting a  baby massage class next week and I think am way more excited than you are, but you hate when I take your clothes off and your lips shiver so I am unsure if you will like it.



Love Mummy xxxxxx

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Sunday, 9 November 2014

The relief of 'I' understand




Going in for the second round of induction on Friday, again me and Dougie left carrying the bags walking into the hospital saying this would be it,we would be leaving this time with a baby but again we left the hospital just the two of us.

Going in on the Friday at two we spent the whole day waiting on the doctor to insert the pessary hormone, I didn't get it put in till 11 at night due to the fact baby Urquhart clearly was not a happy baby and who was moving about to much for over 2 hours its little heart was beating faster than it should of been and doctors wouldn't start till the baby had settled and they could get a decent tracing, but our little baby clearly was not a happy bunny after hours of waiting he/she finally calmed down and got giving the hormone, still hearing I was only a cm ... I just burst into tears for the whole week I had been bouncing on the birthing ball, eating pineapples, which I don't even like, eating spicy curries, drinking raspberry tea and even bought  Clary sage oil for the bath which the woman in Holland and Barrett recommended brings on labour and all of this had no effect and was still the same as I was the week before. Poor Dougie who just cuddled me and told me to have a good cry and made me cry even more by saying good things come to those who wait, I felt anger and hurt I didn't want the first round of induction never mind a second and all because no one would listen and known myself my body and our baby isn't ready. Dougie leaving the hospital just made me cry even more just feeling alone, exhausted and hurt the feeling of just wanting to get up and leave just to be alone in my own bed with Dougie the one person who does understand, the one person who knows how to make me smile, I finally went to sleep thinking I was in a for a long weekend of induction but that all changed in the morning.




 Raspberry leaf tea and Clary Sage oil, still didn't bring on Labour.


Getting myself motivated out the bed in the morning the doctors came round on the ward round and the words of ' why are we doing this ?' would you like to go home ?'  I couldn't believe it after everything I had been told on Monday about the baby not grown properly, the doctor said she wasn't concerned about me or the baby and didn't feel there was any reason to be putting us through all this.  Dougie came to the hospital to pick me up and the anger on his face after everything he went and spoke to the midwife in charge and was saying about putting in a complaint due to the fact of been mucked about so much and told one thing after another by different doctors, the lovely consultant who is the head of the department came and sat down with me and Dougie , We spoke to her about everything that had happened and how the plan changes each time and for once finally someone was listening she looked at all my notes from the cardiologist who has explained how he isn't worried about me during my pregnancy and the fact he explained IST is  harmless, she explained to us she wasn't worried about me or the baby and is happy we aren't induced and left, she has finally took over my care and has even said there's no reason for me to attend the hospital twice a week as long as I see my own midwife once a week and her on a Friday.



The relief of someone looking everything up and understanding my heart and blood pressure was like a huge weight off my shoulders. The whole growth thing with our baby aswell she said how the other doctors have just been over cautious as our baby was a big baby to start with it needs to slow down so there's nothing to worry about. Me and Dougie left the hospital finally happy that things have changed and someones listened, we don't have the worry of going each week to be told something different and feel now I can enjoy my last few weeks of been pregnant with a well deserved rest before baby Urquhart does decide to make an appearance, hopefully soon as its 8 days till our due date and I am getting pretty impatient just wanting to push my pram around and finally meet my little girl or boy.

All of this just proves how very little doctors know about IST ... maybe one day that will all change.



 
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Monday, 13 October 2014

Strong mummies really do make strong babies

Hey Everyone

I should of updated sooner as I have so much to fill you in with and you think with being on Maternity leave I would have all the time in the world... but for me most days are spent at the hospital. I have reached 35 weeks today... and I am so happy and blessed me and baby Urquhart have made it this far with good health, It has definitely  been a rollercoaster but with each passing week I am closer to meeting my little miracle.

After my last post were I spoke about being admitted into hospital again thankfully things have been going a little more smoothly, I still attend the day assessment clinic at the hospital every Tuesday and Friday were I get bloods took my blood pressure, heart rate checked and also baby Urquhart gets a tracing done... who can be one little mr or madam who clearly doesn't like the pressing and the monitor, its only on one occasion he/she was sleepy and not moving and the midwife gave me cold water to wake him or her up to get a decent tracing. Last Friday I was on the monitor for 2 full hours as he/she wouldn't stop moving, the midwife kept saying baby's are active for about 20 mins at a time and then rest not our little baby who was moving so much the midwife finally had to give up after the 2 hours, but on this same day I got another scan to check the fluid around the baby who was seen practicing to breath this time and also he/she has a head of hair already.
Baby Urquhart at 33 weeks 4 days .. he/she was seen practicing breathing and also has a head of hair :)


My 34 week Bump baby Urquhart seems to grow every week and started getting pelvic pain this week, but my heart is still behaving.



This week along with my appointments I managed to spend a night in Glasgow with Dougie were we seen the show Still game, the first time we have had a little night out together in ages :)


                            Me and Dougie enjoyed our night in Glasgow seeing Still game :)


On Friday I had a day booked of appointments at the hospital  my first one was day assessment were they ran an hour behind so ended up having to go to my second appointment  first which was to see anesthetics  were we spoke about my heart history and she advised that in her opnion it was best to have the epidural to control my pain which would help control my heart, I then had my growth scan booked were baby Urquhart is weighing an amazing 5 pound 6 and again we were told Its definitely not a baldy baby, baby Urquhart was seen practicing to breath again and was also pouting its lips this time.
Baby Urquharts little foot :)

  Baby Urquhart at 34 weeks 4 days who definitely isn't a baldy baby and was pouting its lips

After the growth scan I had to go back to day assesment were luckly the doctor came to see me and again baby Urquhart is one monkey who was moving so much the machine was alarming the doctor ended up turning it off. The doctors are happy with the size of baby Urquhart and are hoping I can make it to 37 weeks and may look at inducing me then so I now have appoitments to be seen at the high risk clinic every Friday, me and Dougie are shocked and nervous but excited that we could be meeting our little baby in just 14 days time a whole 3 weeks early.


On Saturday I had the most amazing baby shower thanks to my husband, brother and his girlfriend who done it all for me, baby Urquhart was one spoilt baby who has so much already we are both so lucky to have amazing family and friends in our life who are all so excited to meet baby Urquhart and who all argue already who's getting to babysit first, me and Dougie definitely wouldn't be short of baby sitters.

 The cake my brother and his girlfriend got made :)

 Dougie made all the food.

 Some party games pin the dummy on the baby... mine was the worst.

 Baby Urquhart is one lucky baby.

 Family and friends are everything.
 Twinkle Twinkle little star how we wonder what you are ... after all our scans we still haven't found out boy or girl.... mum still says pink ... dad blue.


Lots of Love and Hugs