Showing posts with label Congenital Heart Defects. Show all posts
Showing posts with label Congenital Heart Defects. Show all posts

Saturday, September 27, 2014

Update

   
Finding beauty everywhere

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Loo Bear has been enjoying the puzzles in the CSIRO's Double Helix magazines.

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Shmoo has been perfecting his gluten free raspberry and lemon friands*. He has now made them several times, including a batch for our homeschool monitor. We had our review (and Loo's initial monitoring visit) in August and it went very well.

*We made the friands with Nuttelex a couple of times so that they were dairy-free and whilst they were okay, they're definitely much better with real butter.

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I'd given up on our cauliflowers and hadn't checked on them too closely for a while. While collecting herbs one morning I glanced over and noticed a huge head of cauliflower. We've had 3 more since and we're also still getting lots of yummy silverbeet, parsley, kale and beetroot.  Shmoo has taken to helping me weed the beds and keep an eye on the developing cabbage heads.

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The last few months I've been getting back into making our own yoghurt and have even branched out into making labneh. So easy and yummy.

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We had fun making some bird feeders recently. The OH poked a hole in the bottom of 5 plastic cups. We then used a length of kitchen string to tie 2 craft sticks in an 'X' shape and threaded the other end through the hole inside the cup and securing to the outside with sticky tape. Repeated for all 5 cups. We mixed 1kg wild bird seed mix with 250g softened lard. The boys packed the seed mixture into the cups; removed the tape; and pulled the string tight so that the craft sticks rested snugly against the top of the cups. We froze the cups for a few minutes until they had set and then removed the seed mix from the cups and hung them up outside.

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Baby Bear had a cardiology review a while ago. At 18 months old he was not impressed with being stripped down in front of strangers in a strange environment, attached to strange machines, and poked with strange equipment. He put up with being weighed (9.29kg with a nappy on - below the 3rd centile line still) and then cracked it. He was very vocal about his displeasure. I breastfed him through the ECG and that somewhat distracted him but by the time we got to the echo he was totally over it. He wouldn't feed anymore and refused to be distracted by the apps on my mobile. They couldn't really get a good view of his heart because of his screaming and squirming around but it looked like there probably wasn't anything 'significant'. The cardiologist was happy enough to schedule the next review for 2 years time, when Baby Bear should be old enough to be a bit more cooperative and allow us a better look at his heart.

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It's been a tough winter with us seeming to catch a cold or flu every 2-4 weeks for the past 3 months. The last cold has left Baby Bear with a mild chest infection and a horrible case of oral thrush. His mouth is causing him a lot of pain and I haven't been able to brush his teeth because he screams and his mouth and gums bleed so much. Our GP has just put Baby Bear on antibiotics 3 times a day for the chest infection and to make sure nothing nasty has gotten to his heart through his mouth. He's also on nilstat 4 times a day for the thrush. Poor baby. He's terrible at taking meds and I'm also giving him probiotics, kefir grains, xylitol and coconut oil so it feels like I'm trying to coax him into opening his mouth all day. Fingers crossed that it all clears up very quickly! 

Tuesday, May 6, 2014

ANZAC Park, Ulverstone

  

Stopped by a HeartKids get together... A gorgeous, sunny autumn afternoon, perfect for a spot of climbing and seagull chasing. Baby Bear was so excited to see the gulls, pointing and saying "Duh, duh," thinking they were ducks.

Seeing him running around so confidently did make me realise that he's been walking for about 2.5 months now. Definitely time for his first pair of shoes!

Tuesday, March 4, 2014

HeartKids Birthday Card

Baby Bear received a birthday card in the mail today... from HeartKids! What a lovely surprise!

I never made it to any of the HeartKids Thursday morning teas at the hospital but I certainly appreciated their visits to Baby Bear's room. It made the hospital stays and surgery just that little bit less lonely and scary.

And speaking of hospital stays, I've just realised that in 2 days it will be 1 year exactly since Baby Bear's CHD diagnosis and first hospital visit. Wow, a whole year. And what a year it's been!

Saturday, November 2, 2013

Heart Baby - Things I've Learned

Things I've learned from our surgery and hospital experiences with a young heart baby...

- It doesn't help to blame yourself.

- Be realistic. Neither pessimism or blind optimism helps.

- Read up, ask questions, be informed. But don't go overboard and don't diagnose with Dr. Google.

- Look up some photos of post-op heart babies in ICU. It's best to be prepared because it can be hugely overwhelming to walk into ICU and see your tiny bubba lying there so still, on a ventilator with lines and drains and wires all over them.

- Familiarise yourself with the medical jargon.

- Find out what support is available (eg. the Patient Transport Assistance Scheme). Usually the hospital will be able to give you info on what assistance is available to you.

- Get a display folder to keep paperwork in.

- Have a notebook that you can jot down questions and information. It's so easy to forget things!

- If at all possible, don't do it alone. It gets very overwhelming, especially if you have to travel away from home to an unfamiliar city. It would have been so much better if I'd had someone with me for all the appointments and hospital stays.

- It is possible to breastfeed a heart baby (maybe fully, maybe with EBM, maybe with a calorie supplement, maybe with formula supplements... depending on baby's condition). Get in contact with the Australian Breastfeeding Association or others who have been in similar circumstances.

- You may come across the odd doctor or paediatrician who's very anti-breastfeeding. Try not to let them get to you and find another doctor if possible. Listen to the doctors who are supportive. (I had lots of health professionals who were supportive. Once I knew B was okay I cancelled our appointments with the paed-who-thought-he-was-God).

- See a lactation consultant to make sure baby's feeding optimally.

- Poly-Joule mixes easier with fresh, warm expressed breastmilk. Then sit it in the fridge for at least an hour or so before use.

- Use your smartphone to set alarms for meds or buy a specific medicine alarm (some of them are really cheap).

- If you live outside the metropolitan area, check with your local pharmacy to see how long it will take to get baby's regular meds and supplements in.

- If you know something's not right or it seems like the docs have the wrong info, keep telling someone until you're listened to.

- Print out a map of the hospital if you're not already familiar with the place. Find out where the waiting areas, parenting rooms, and cafes are. Look into nearby accommodation (if you don't live nearby) as well as which shops, parks and transport are close by.

- Think about if you'll be staying in hospital with baby or elsewhere. Where will you stay while baby's post-op in ICU? (I could only room-in with B once he was transferred to the cardiac ward about 24 hours post-op. Many babes stay in ICU longer than that.)

- Find out what the hospital provides... nappies, dummies, meals, formula?

- Pack enough clothing so that you've still got clean stuff even when baby's puked all over you several times during the day and spat meds out, dripped blood from tests etc. Consider washing facilities and clothing drying times. It's not so much of an issue if you're close to home but don't under pack if you're travelling interstate!

- Keep in mind that the wards are usually quite warm (babies only wear nappies for several days post-op) so pack appropriate clothing for that as well as the outside weather.

- Pack tissues. There were some tough days when I really needed them!

- Leave a bit of luggage space so you've got room for paperwork and meds when you go home.

- If you usually put baby in sleeping or swaddle bags make sure the bags have a 2 way zip so that when baby is able to wear them post-op the monitoring wires can be hooked up through the bottom of the zipper. (Put baby into the sleeping bag before attaching the wires).

- Pack a few pens... they always seem to go missing in hospitals.

- It's a good idea to take some snacks and a bottle of water. Don't forget to take any meds or supplements of your own and consider food options if you have any particular dietary requirements. Pack your favourite toiletry items but it's not the best time to try new strongly scented products - baby will likely find comfort in your familiar scent post-op.

- Pack a couple of baby's favourite toys and anything that may be of comfort post-op. I had a particular playlist that I put on my phone, music that I'd been playing a lot for B in the weeks before. I also took his massage oil as I've given him regular massages since birth and he finds it soothing (in the first couple of days post-op, massaging was often the only thing that comforted him when he was so hungry but on fluid restrictions). It's also handy to pack baby nail clippers so they don't end up scratching themselves.

- I printed and laminated family photos to take as well as drawings by the other kids. Post-op, a photo of his brothers propped up in his hospital cot would cheer B up and amuse him for a while.

- Consider what you'll do while baby is in surgery. It's a very long wait and the hours drag by. Catch up with friends, go see a movie, or do some shopping if you feel up to it. If you'd prefer to stay at or close to the hospital, make sure you've got a book or laptop/smartphone to keep you occupied.

- Love my smartphone. Not only could I keep in contact with friends and family but I could also use it to surf the net, record info, play games, take photos, listen to music and read ebooks.

- If you are breastfeeding don't forget to express while baby is in surgery, at least as often as baby normally feeds. Talk to the post-op ward or ICU about storing EBM. It will take at least a day or two, maybe more before baby is allowed to (or interested in) breastfeed post-op so keep expressing regularly, especially overnight. B continued to have some EBM via a syringe for a while. Be prepared for baby to have some difficulty with feeding for a while, particularly while the drains and pacing wires are still in place (they can be uncomfortable for baby). Ask to see a lactation consultant if you're concerned about breastfeeding progress.

- Even if baby doesn't normally take one, a dummy may provide some much needed comfort in the early days after surgery, especially for a breastfed baby who isn't allowed unrestricted breastfeeds yet.

- Learn how the sats monitors, BP cuff etc are hooked up to baby and what the different monitors are for. (The nurses don't mind giving a run down on what they're doing each time they do obs and, in my experience, most give explanations without being asked). It's handy know the basic things so, if necessary, you can hook baby up yourself after a feed/cuddle/weigh as it can get pretty busy on the ward especially when another child has had a medical emergency and almost all the nurses are attending that.

- Try not to panic if one of baby's monitors goes off. If baby looks okay and a cavalcade of doctors and nurses doesn't suddenly fill the room, then chances are it's nothing serious.

- Every nurse has a different attitude towards obs. Some are really strict and will wake baby up to do them, some are very relaxed and will let you buzz them once baby's woken and do the obs then.

- Try and keep track of when baby's meds, obs or various procedures are due (ask the new nurse at each shift change as they'll have just been updated). You'll then be able to buzz your nurse before baby falls asleep. (Soooo many times B finally fell asleep only to have a nurse come by 10 minutes later for meds or obs!).

- Don't feel bad if you can't remember everyone's names.

- It's easier to find a vein for taking blood when baby's had a recent feed.

- If doing pre- and post-feed weighs and recording feed times and durations, do it yourself and then write the info down (even on a paper towel) and then leave it on the desk or tray table so the nurse can record the info next time they come by. Same for nappies if they're weighing them - record nappy change time and leave the bagged nappy next to the info. This way you don't have to buzz the nurse every time. It's also good for overnight - you can record the info and go straight back to sleep without having to wait to fill the nurse in on every little detail.

- Do as much for your baby as you feel comfortable doing but know when you need to step back. I couldn't bear to hold or be next to B while they catheterised him for nasal and urine samples - I was crying as much as he was!

- Ask for help when you need it. As a mum of 4, I've changed my fair share of nappies but changing a dirty nappy on a post-op baby who has tubes and lines all over him is something else altogether. It took maybe 2-3 days before I could do it solo. Also, I'm a fairly experienced breastfeeder but settling down to feed a post-op baby tangled in all the monitoring wires, lines and drains is tricky!

- It's okay to leave baby and go and grab a cuppa. It's also okay if you don't. Personally, I couldn't bring myself to be apart from B as I was on my own there with him with no one else who would be familiar to him. The nurses often seemed busy with babies whose parents weren't able to stay with them and I hated to think of B crying for extended periods if I wasn't there.

- If you don't want to leave baby, find out when baby is well enough to go off the ward and go for a short walk together.

- Make the most of the hospital volunteers. They'll keep an eye on baby while you have a cuppa, finish your meal or have a power nap.

- Nap when baby does during the day. Close the door and curtains overnight to help cut out some of the noise and light.

- It's totally normal to feel completely overwhelmed at times; maybe perfectly fine and coping one minute and falling apart the next. In hospital a day can feel like a week and circumstances can change quickly. Ask to speak to the social worker if you need to. Find someone who's happy to listen to you debrief, even a friend or family member over the phone (or even just write/type it all out)

- Sucrose (sugar water) may help to keep baby calmer during painful procedures. Ask if it's not offered.

- Immediately prior to having a heel prick done, firmly massage a very warm, wet cloth against baby's heel. This helps to get the blood flowing and hopefully not so much squeezing will be required (squeezing the heel may affect the results and leave baby sore and upset). If it seems to be difficult getting enough blood from a heel prick, ask if the ward doctor can take it via the back of baby's hand instead... sometimes it's just quicker and easier.

- For a few weeks post-op, the hiccups would make B cry. Coughing would make him cry. Sneezing would make him cry. Crying would make him cry. It all hurt his sternum. He hated Panadol so even the pain relief would make him cry.

- Baby won't be able to be picked up and held under the armpits for a good 6 weeks or so. Consider how you'll go travelling with baby if you have to fly home. It's definitely easier if you've got someone else to assist you.

- Consider post-op accommodation. We were told that the average hospital stay after an uncomplicated VSD surgery is 7-10 days. Despite a couple of little post-op bumps in the road to recovery, B was discharged on day 5. We had to stick around until a post-op check on day 8 but weren't allowed to fly until day 10. With the help of the hospital we were lucky enough to get a room at Ronald McDonald House.

- Meds are likely for at least a few weeks post-op.

- Scarring. Pre-surgery, looking at photos of little heart babies with a great big scar down their chest was enough to reduce me to tears. Post-surgery it doesn't seem so bad. Yes there's a big scar - which they say will grow with him but will also fade a lot in time - but I don't see it as something 'bad', as something 'wrong'. I see it representing his heart being healed, fixed. Plus his brothers seem to think it's pretty cool, and I'm sure B will think the same when he's older. That's his main scar. He also has half a dozen small scar 'spots' just below it from where the drains and pacing wires were stitched in place. He has another small scar on his neck where the central line was placed; and another couple of barely visible scars on his hands/feet from the peripheral lines.

Thursday, August 1, 2013

Cardiology Review

We had an appointment with Baby Bear's cardiologist (who we can't think of without being reminded of the Aqua song... Dr Jones, Dr Jones, calling Dr Jones...). Fortunately he was in Launceston rather than us having to fly all the way to Melbourne.

Baby Bear had the standard ECG and echo. He still has the small VSD and leak at the edge of the patch but, again, they're confident that they'll eventually close on their own. In fact, Dr Jones was so happy with Baby Bear's progress that he doesn't need to see him now for another year!

Friday, July 12, 2013

Tiny Bubba

It never fails to surprise me just how small Baby Bear is. I was going through the other boys' records and they weighed the same as Baby Bear (5 months in 2 days time) when they were 2-2.5 months old.

Wednesday, July 10, 2013

Back Carry

And I can now carry Baby Bear on my back. So nice to be able to get stuff done and carry him around at the same time. He's very much an 'in arms' baby... no wonder too after everything he has been through! I managed to get a batch of kefir done this morning while he slept peacefully on my back in the Storchenwiege.

Monday, July 8, 2013

Six Weeks Post-Op

He's doing so well :) He weighs 5.57kg, had his last dose of Frusemide this morning and can now be picked up under the arms and have tummy time again.

Tuesday, June 25, 2013

Cardiology Review

Yesterday Baby Bear had a review at the RCH in Melbourne. It was a loooong day.

Our flight left at 6.30 am and was scheduled to arrive at 7.45. However a Stephen King fog descended over Melbourne (it came in eerily thick and fast) and after one attempt at landing our pilot decided it was too risky. Our plane was diverted to Mangalore, a tiny regional airport, where we waited in the freezing cold for the fog to clear. I called the hospital from there and thankfully they were very understanding. At 9.50 am we were in the air again but had to circle above Melbourne for over an hour as we waited for our turn to land. We finally landed at about 11.30 am and it was nearly 12.30 pm by the time I got to the hospital... 1.5 hours late for the appointment. Luckily I'd gotten PTAS to book us on the evening flight back instead of the mid-afternoon one.

B had another echo and ECG and it's all looking good. Still a slight leak at the edge of the patch and the 2nd tiny VSD is possibly still there but they're not concerned about them. He is now off the captopril and is down to one dose of frusemide for the next 2 weeks and then no more meds at all! His next check up will be in August when the cardiologist comes over to Launceston.

B also had his 2nd dose of the RSV immunoglobulin. Ideally he'd have more, til the end of winter, but they can only give them at the RCH so they think it's better that he had 2 doses than none.

So that was it, hopefully our last medical trip to Melbourne!

Friday, June 14, 2013

Perspective

While Baby Bear was in surgery I met people whose children had heart problems that required them to repeatedly spend weeks at a time at the hospital.

In ICU I whiled away the late night hours with another woman who also didn't have accommodation that night, a mother whose pre-teen daughter was critically ill due to a brain tumour.

At Ronald McDonald House I chatted with the mother of a young toddler. They'd been there for 4 months and looked set to spend at least another 4 there.

I am so grateful that Baby Bear is doing okay, that he is recovering so well from the surgery, that his patched up heart is doing just fine and although he's still a little sore he's healing wonderfully. He is still on frusemide and captopril for now but probably not for long. He feeds easier and breathes easier. He's putting on weight and is now just under 5kg. My amazing boy. :)

Monday, June 3, 2013

We're Going Home!

Just because B can't fly doesn't mean we can't get back to Tasmania. PTAS have booked us on the Spirit of Tasmania tomorrow night. :)

Saturday, June 1, 2013

Discharged

Ironically, we spent 8 days in hospital when B was 3 weeks old while they fiddled about with his meds and yet here we are, 5 days after open heart surgery and they've discharged us.

We're at Ronald McDonald House while we wait for B to be able to travel home. We have to go back to the RCH on Tuesday morning for clinic so that B can have the sutures removed from his drain sites.

Feeling awfully miserable and homesick at the moment. I miss my family. :(

Just got the go ahead to go home from the ward doc! Except she forgot that we are from Tasmania and can't fly for 10 days after cardiac surgery. Good to know Baby Bear's looking that good though.

Friday, May 31, 2013

Clean and Clothed

We gave B a 'bed bath' this evening. After his poo explosion yesterday and being covered in residual stickiness from all the dots, tape and dressings, he definitely needed it.
Then he got to put on clothes. They've just decided to keep the last peripheral line in his foot for now as a precaution and it doesn't fit in his growsuit so we left that foot out. His swaddle bag went nicely over the top. I put him in it, pulled the bottom zip up a little and threaded all his monitoring wires through before hooking them back up again. Snuggly. :)
Oh and today he had his nasogastric tube out. He also had another echocardiogram and ECG as well as a chest xray. Echo and ECG were fine except the echo did show a tiny leak at the edge of the patch and they found that 2nd VSD again but it is smaller and they are confident that both things will close by themselves in time. The chest xray showed a few dark patches on his lungs. Shouldn't mean any major problems, just something they're keeping an eye on.