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teddyhasaspecialheart

~ My Little Boy's Fontan Journey

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Author Archives: carolyngalvin

Details for tomorrow

24 Tuesday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 3 Comments

 

 

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We need to be at the hospital ready to start at 6:45am Wednesday so we will be getting Ted up just after 5am so he can have some water ahead of our drive out to the hospital.

He is fasting from midnight but at least he can have water until 5:45am.

Ted will be in theatre for hours and we are unlikely to get any updates until it is time for them to take him off bypass when often one of the surgeons will give us some feedback on how it has gone so far.

It will be a while before we will then get to see him in ICU and I anticipate we will have our phones off so please understand if we aren’t replying to messages. I hope nobody worries, do not take silence as an indication of how things are going. Please just know we are focusing all our energy on our precious Ted, the hospital environment can be so stressful.

As soon as we know something we will update here via the blog. It may be a little while before Ted is ok for visitors but we will pass on all your love and messages. xx

 

Fontan Eve

24 Tuesday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 8 Comments

Like Christmas Eve. But not.

We tried very hard today to have a fun time with Ted ahead of his big surgery tomorrow. It is always hard to play with a heavy heart but Ted is such a fun little guy we are lucky he kept us smiling. He said he really enjoyed his day in fact he told Tabitha “today is MY day you know, not yours, because I’m extra special” she gave him a very unimpressed look the kind best given by a 7yr old big sister.

Here are some photos from our little picnic at the park and our fun stopover at the playground. We had lots of delicious treats and tonight ended the day with Ted’s favourite dinner- lasagne!

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We are so touched by all of the messages of love and support and Teddy was so chuffed to receive so many special gifts today, he will be the most loved boy in all the hospital. Thank you so much to our amazing friends and family we love you all so much! xxx

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Ted needs your blood!

24 Tuesday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 4 Comments

Tags

blood, blood bank, bypass, CHD, child surgery, donate life, Fontan, give blood, HLHS, Open Heart Surgery, operating room, red cross, transfusion

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So many wonderful people have asked how they can help Ted and our family. We are so grateful for the meals some of our kind friends are making as it is so so so helpful! Another way to help is to donate blood.

It is really easy to go to your nearest Red Cross Blood Bank. It doesn’t take long.

Every time Ted has open heart surgery it is necessary for the surgeon to stop his heart. He is then hooked up to an amazing  heart-lung machine (cardiopulmonary bypass) that then takes over the job of his heart, lungs and kidneys for the duration of the surgery.

The operating room will be packed full of people tomorrow including a team of perfusionists who operate the bypass machine aided by loads and loads of donor blood. So if you are able to spare a bit then please save a life or two.

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Two sleeps

23 Monday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 11 Comments

Tags

anticipation, CHD, Children's Hospital Westmead, chronic illness, Fontan, HLHS, Open Heart Surgery, staph, surgery

“Two more sleeps til my operation, I’m scared I might die.”

Ted’s words today came at me like a very sharp kick in the guts.

There is no terror in the bang, only in the anticipation of it.

Alfred Hitchcock

Anticipation is indeed something that can terrorise even the littlest of people.  Knowing Ted, this is why I chose only to drip feed tiny bits of information to him about his operation. I don’t know how he made the correlation between his surgery and the very real risk of death but he did. And it was a very sad thing to hear.

We are doing our best to put his mind at ease, all the while hiding our own very real fears. This is a challenge in itself. One of the hardest things on the day of surgery is making the very long drive out to Westmead pretending to be chipper for Ted’s sake but feeling the dread building with every kilometre. Such a hellish drive. Then the long walk to the anaesthetic bay, that’s another journey we try to make fun for Ted while fighting back massive sobs.

Today and tomorrow we have to wash Ted in this weird pre-op stuff that smells like flea shampoo (he is Staph A positive) but it has the added bonus of giving him cute hair: 

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Rich and I will spend the day with Ted tomorrow being an only child for a day, doing fun things ahead of Wednesday. Wednesday won’t be fun. Today after dropping Tabitha at school at 8 o’clock in the morning I let Ted have this green frog cake full of sugar and rubbish. Just because.

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A tricky morning that ended well

20 Friday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 1 Comment

Cheerful Ted was my little ray of sunshine this morning. After an unfortunate car crash after dropping Monte at daycare this morning (my fault~oh gosh) Ted told me he knew how to cheer me up.

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He suggested we play ‘angry birds’ with Lego because “that always makes me happy mama”. This little fellow was right. It did cheer me up, just seeing his funny smiling face with his little lego game in play.

A smile is a curve that sets everything straight.

Phyllis Diller

Biding our time

19 Thursday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 2 Comments

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With six days til surgery, we are trying to distract Teddy from noticing that he is essentially under house arrest! Since we have to keep him isolated so that he avoids another infection he has been feeling quite put out that he can’t have his regular babycino at the local cafe with Monte while Tabitha is at school so we have been making babycinos and special treats at home. We even resorted to bathing our dog Beatrice this morning. Fun for Ted and Monte. Not so much for Beatrice! I explained to her that we all must make sacrifices for those less fortunate but still she has this face on:

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Ted was so chuffed yesterday that one of his dearest friends from school Ari had sent him a special package from Japan. This little air-doctor virus protection badge, Ted and I have no idea how it works but Ted loves it all the same and has been proudly wearing it all day. Thank you so much gorgeous Ari! So thoughtful.

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Last week Tina a wonderful friend of mine from Melbourne sent up a most amazing parcel for Ted. She has hand-made beautiful superhero comic pjs for teddy and a beautiful doll that also has a ‘zipper’ on his chest and a special heart. Like Ted. We can’t wait to take all these special gifts with us to hospital knowing how everything has been given with so much love for Ted makes wearing it even more special for him.

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Ted may only have half a heart but it is full to the brim with love from all of his friends. Near and far, we have been buoyed by the messages of love and the offers of support from people everywhere. Particularly our Redlands family.

We are so blessed to have such an amazing group of parents from Ted’s class who have arranged an online care calendar to help us out with meals while Ted is in the hospital. I can’t express how very grateful I am for this support since there really is nothing nutritious for Ted and I at Westmead. Last time he was out there he was offered a stale white bread sandwich with a sachet of peanut butter for lunch. The cafeteria has food parents can buy like chicken nuggets and other yellow globs of who knows what. It is such a shame that the food situation out there is like that for sick kids and their families.

Rich will be taking time off work as much as he is able but he will be juggling our other two at home and let’s face it the man has many talents but cooking isn’t one of them! So as a mum it really warms my heart to know that there are people out there looking out for my family at home and helping out with meals for them. Thank you all so very much, we are truly blessed to have you all in our life. xx

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A very important date

17 Tuesday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 7 Comments

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So pleased that Ted’s surgeon has rescheduled surgery for next week!
Wednesday 25 February
We will keep ‘bubble boy ‘ isolated til then in the hope that no more germs make their way in here!

Awaiting a new date

16 Monday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 3 Comments

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My poorly little bedfellow above is now awaiting a new surgical date.
His surgeon says he will have a new date tomorrow. Praying we do not have a long wait. A week would be ideal, Ted’s cardiologist said it will more like 2-4 weeks. Hope not…

Not looking good at all…

14 Saturday Feb 2015

Posted by carolyngalvin in Uncategorized

≈ 6 Comments

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Well, it certainly looks likely that Ted’s surgery will be cancelled for this week.

He has now developed a fever, feels yucky and has a rash on his neck.

So very disappointing. We reconvene with the surgeon on Monday but I am almost 99% sure he will cancel.

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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.

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