Just before Christmas a friend of mine got a new family pet, a Bichon Frisse dog called Arthur.
As soon as they met, Omar and Arthur became great buddies. It’s the first time Omar has been this close to a dog and it was so cute to see how happy he was to meet Arthur!
The photos aren’t great, I was taking them with my phone whilst holding Zaki, but I really wanted to capture how excited Omar was by Arthur the pup.
That being said, we won’t be getting a dog. Ever. There’s enough mayhem in this house as it is! But at least I’m now prepared for the fact that Omar is probably going to be one of those kids that asks if we can get a dog 50 times a day between the age of 4 and 16. (My brother was also one of those kids.)
If you’re thinking of getting a dog, it seems Bichon Frisse’s are child-friendly. Arthur was just as happy to meet Omar as Omar was to meet him and I was never once worried that he was going to bite or nip him. If he can put up with Omar he can probably put up with anything.
I really envy those people that find cooking therapeutic/satisfying/fun or whatever. To me it’s just a chore. When I put my mind to it I’m not a bad cook, I just find it so dull and feel like my time could be better spent elsewhere, rather than in the kitchen, so I usually take the easy option and cobble together fail proof meals that take minutes rather than hours. Old faithfuls like cottage pie and spag bol.
But once in a while I will make a complicated Middle-Eastern rice dish or an Algerian favourite of my husband’s, such as the dish in the photo above. It’s my husband’s absolute fave and it actually tastes a lot better than it looks or sounds.
The main ingredients are 1 small onion, 3 or 4 cloves of garlic, 3 chicken pieces on the bone, 3 medium potatoes, 2 eggs and usually chick peas (but I didn’t have any in so I missed those out).
First of all the onion is chopped, the garlic is crushed and they are lightly fried in olive oil in a medium sized pan. Then the chicken is added to the pan for a couple of minutes, along with salt, pepper and ground mixed spice to taste. Water is then added – just enough to cover the chicken – bring to the boil and then simmer for around 20 minutes.
This is the weird part (well I think it is) – while that is going on peel the potatoes and cut into chips. Sprinkle with salt and then fry in oil (or use some other healthier method). Once cooked transfer to a frying pan and pour 2 whisked eggs over them. Then fry. (Yep, you are making a chip omelette. Told you it was weird.)
Once the chicken is cooked throw the chip omelette into the pan and sprinkle with fresh parsley. Once it’s dished up some fresh lemon juice really adds to the flavour.
I know it sounds odd to our sensible British pallets but it’s actually pretty tasty, honest. Calorie-wise we’re probably talking thousands though so be warned if you ever happen upon this dish. (Highly unlikely unless you’re planning a trip to Algeria!)
February is Congenital Heart Defect Awareness month. You might have read my post about my baby, Zaki and his broken heart and how his life was saved by some amazing cardiologists, surgeons, consultants and nurses. Our outcome was a happy one but we all would’ve found it so much easier to cope if we’d been aware and been prepared.
Before Zaki was born I knew absolutely nothing about congenital heart defects and assumed that if there was anything wrong with my baby’s heart it would have been picked up at my 20 week anomaly scan. Wrong. Only 50% of the type of defect Zaki had are spotted during the anomaly scan. When I was told about the diagnosis I wish I’d known more about it; instead I felt confused and helpless. I’m passionate about raising awareness wherever I can now, so here are some helpful facts about congenital heart defects:
Congenital heart defects are problems that have occurred with the structure of the heart as it was formed (‘the plumbing’)
There are 18 recognised main congenital heart defects, with variations of each one
1% of babies will be born with a congenital heart defect and it is the most common defect in newborns
That’s 12 babies a day in the UK that are affected
Out of those 12 babies, 4 will have been diagnosed pre-natally, 4 will be diagnosed shortly after birth and 4 will go home undiagnosed until they fall ill or die
The heart is formed within the first 6 weeks of a foetus’ life and the defect has probably occurred before the mother even knows she is pregnant
Congenital heart defects kill twice as many children as all childhood cancers combined
Scary stuff isn’t it? But it isn’t all bad news. With early intervention 90% of babies born with a congenital heart defect go on to live happy, long lives.
There really isn’t anything a mother can do to prevent her baby being born with a congenital heart defect but there are steps that can be taken to make sure it’s picked up as soon as possible.
At the 20 week anomaly scan the following questions can be asked of the sonographer:
Can you see the 4 chambers of the heart?
Are there 2 upper chambers and are they controlling the blood flowing out of them with valves?
Are there 2 lower chambers and are they controlling blood flowing out of them with valves?
Do the two great arteries (aorta and pulmonary artery) cross over each other as they exit the heart?
Are there any holes in the wall between the two lower chambers?
Can you see any abnormalitiesat all with the heart?
If you are pregnant, write those questions down, take them with you and ask. It’s worth it. The sonographer might not be able to answer all of those questions and might put it down to the position of the baby. If that happens offer to go for a walk and come back in 10 minutes. You might sound like a pushy mother-to-be but who cares? It might just save your baby’s life. I so wish I had asked those questions. Knowing about a congenital heart defect prior to the birth increases the baby’s chances of survival and also means the parents can mentally (and practically) prepare themselves for what’s to come.
There’s an amazing charity called Tiny Tickers who do great work in funding training for sonographers so that more CHD’s will be spotted at the anomaly scan. You can order a card free of charge from the Tiny Tickers website here which you and the sonographer can go through together at your scan if you’d prefer to do that rather than ask the questions above.
If a congenital heart defect isn’t picked up at the 20 week anomaly scan there are signs and symptoms that might become apparent once the baby is born:
Cyanosis (skin looks blue, especially hands and feet)
No interest in feeding
Fatigue (baby will not wake)
If you have any concerns AT ALL please insist that a pulse oximetry test is carried out on your baby. It’s a really quick, non invasive test that involves a sensor being placed on a finger or toe. The oxygen saturation levels (sats) in the blood can be measured that way and if they are lower than expected, that suggests a problem with heart function and further tests can then be carried out to establish exactly what’s going on.
Don’t be embarrassed/shy/too polite to ask for that test to be carried out if you are genuinely worried that your newborn isn’t behaving as he or she should. That simple sats test saved my baby’s life. (For the first time, his life was about to get saved several times over the following weeks but that’s another story.) Don’t sit there quietly panicking, just explain your worries and ask for the test.
If you go home with your baby and later notice something isn’t quite right go to a&e. Heart defects are time critical and every second matters. Don’t worry that you are being over-cautious, just get your baby checked out. Your instinct might save their life.
Of course 99% of babies do not have a congenital heart defect so please do not let this post worry you sick. The chances are that your baby will be absolutely fine. But it doesn’t hurt to be prepared. Something that I definitely wasn’t when I was told there was something wrong with my baby’s heart a few hours after I had given birth.
If you find yourself in the position that I was in try to take comfort in the fact that the cardiologists and surgeons will do absolutely everything possible to save your baby and above all else, stay strong.
Look at what a lucky girl I am this year! I have all of these cards and gifts to open in the morning. And to make it even more exciting I haven’t a clue what a single one of those presents is!
My husband isn’t usually great at getting organised for things like birthdays but this year he’s made a real effort and there are even cards in that pile from each of the kids. I really don’t mind what the presents are or how many there are and I’m sure there’s nothing flashy, but I’m just so appreciative that a huge effort has been made.
When I was younger my mum always used to love receiving cards with lovely verses inside and if she was ever choosing a card for someone she would take an age picking one that conveyed the message she wanted to give. I didn’t understand, I barely read the cards and was all about the presents. But now I really get it. I can’t wait to read those cards in the morning.
Shout out to Zaki who was born with a heart defect but has always been perfect to me ❤️.
February is congenital heart defect awareness month. If you would like to donate to the Children’s Heart Surgery Fund please text Wear16 and the amount to 70070. We are forever grateful to them for what they did for Zaki ❤️❤️❤️❤️❤️.