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teddyhasaspecialheart

~ My Little Boy's Fontan Journey

teddyhasaspecialheart

Tag Archives: pre-admission clinic

Today we won!

13 Friday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 6 Comments

Tags

CHD, Children's Hospital Westmead, HLHS, needle phobia, play therapy, pre-admission clinic, public hospital, surgery

Ted and I left home before 8 o clock this morning and we got home late in the afternoon. It was a very long day for Ted but from start to finish he was the bravest of the brave. I never expected our day to run so smoothly.

As I mentioned yesterday, my relationship with the hospital is one of love and hate. I love our team of amazing specialists, the doctors and nurses who are our heroes at The Heart Centre for Children but I absolutely hate the bureaucracy of the public system.

While we are private patients in a public hospital this means nothing other than for billing purposes. We still get lumped in a shared room with 5 other kids and their families. Excellent for disease control, not to mention privacy… Everything is geared toward the lowest common denominator. Instead of hold music when you ring the hospital you get patronising recordings about keeping hot drinks away from young children and why shaking babies is not safe. Toys are often fixed so that they can’t be stolen. It is a bit of a freak show out there to be quite honest. I could go on forever but I won’t. Just yet.

Our day began with a dash to the hospital pharmacy where they charged me $78 for a small tube of numbing cream for Ted’s blood test. See that right there is really sad. Many children would have to put up with the pain when costs are that high.

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Things looked up from that point on because our amazing play therapist met us at the Heart Centre lobby and Ted immediately perked up and enjoyed playing with the toys. She stayed with Ted the entire day, we couldn’t have done it without her.

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After appointments with his anaesthetist and the genetic researchers (we are participating in the whole-genome sequencing project as well as the Fontan Registry)  Ted had an ECG.

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Then some x-rays

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Then it was the moment we have been preparing Ted for… the blood test. He blew everyone away with his bravery. He didn’t flinch. He played Angry Birds on the iPad and Karen and I spoke to him the whole time. He was truly amazing. Normally we have to restrain him with the help of a few others. The preparation paid off.

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After doing some Angry Bird craft in the waiting room we took Ted to the Starlight Room for a break. He loved playing with Captain Starlight and playing the drums like his Papa.

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We met with some more doctors and Teddy was beautifully polite and compliant putting up with a lot of poking and prodding for one little boy on one big day. 



 I promised Ted he could choose a small toy from the gift shop for being so brave and beautifully behaved. He chose the biggest toy they had. Of course.

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We have been given the all clear for surgery on Wednesday provided the cough remains as is and he doesn’t develop fevers or other signs of a cold. We have had to up the ante on the asthma meds as he was struggling a little today. We are praying the cough settles over the weekend as it does seem to be worsening a little today…

Unfortunately Ted’s big sister has a bad case of tonsillitis and his baby brother is the sickest I’ve ever seen him with croup. We have had a few emergency doctor trips with little Monte this week. I’m praying the poor fellow starts to improve this weekend. It breaks my heart to think of being apart from my other children next week especially when they are so unwell. Ted is staying with Grandma tonight, we are trying to quarantine the sibling germs.

Friday will be a big day for Teddy

12 Thursday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 6 Comments

Tags

Australian healthcare, bureaucracy, chronic illness, communist, Fontan, get to the back of the line, pre-admission clinic, public hospitals, red tape, yes minister

Tomorrow Ted and I have to be at The Children’s Hospital Westmead by 9 am for his pre-admission clinic. It represents everything our underfunded public hospitals stand for~ queues, red tape, frustrating people and pain. Excellent. My kind of place, my kind of day. My love-hate relationship with this hospital will be a common thread in my upcoming posts I am sure.

Pre-admission clinic is a day of testing for Ted. Imaging, pathology and consults with some of the medical staff who will assist in his post operative care next week. We have done quite a lot of preparation for tomorrow. Ted has a very significant needle phobia and together with his child-life therapist we have tried to desensitise Ted to the process through play.

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How this works tomorrow will set the tone for his Fontan recovery since Fontan (& Warfarin) brings with it many months of needles. We are praying for tomorrow to go as smoothly as possible for Ted, and also for me to control my temper. I’m not good with mindless bureaucracy at the best of times, add my child suffering in to the mix and you have yourself one very tricky customer.

In case anyone is wondering, no we did not choose to go to Westmead for Ted’s care! It was selected by default.  Here in Australia we have three hospitals to choose from when planning to deliver a baby with HLHS. Here in Sydney we have only Westmead and there is another hospital in Melbourne and now another in Brisbane.  If we could go through the private hospital system we would. Believe me we would do anything to avoid being in-patients in the public system, anything to expedite red tape and actually feel like a respected person not a prisoner… Alas we do not have those options when it comes to paediatric cardiology in Australia. It is very different in the US.

Ted’s cough is stable and I am praying that his chest x-ray tomorrow does not reveal any nasties. Unfortunately Tabitha, Monte and I are all very unwell at the moment and now even Grandad has come down with this awful bug. So far we think Ted has escaped the worst of it… Perhaps his lucky escape is due to the loving care he has received from the mum of his special friend and classmate Mitchell. This week Mitchy’s mum has been bringing Teddy some beautiful Chinese broths and congees to keep his cough at bay and we are so grateful to her. She is a real blessing!

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