After weeks of pestering, Ethan can now watch his own trainset on YouTube, as well as everyone else's.
Tuesday, April 28, 2009
Thursday, January 15, 2009
Merimbula
It brings me much joy to be able to sit and type about Eth turning 7 tomorrow. I thought it would never happen and that his 6th birthday would be the last. This time last year he was in heaps of pain, his mobility was extremely restricted and he couldn't eat properly. It was a very tough time but I am pleased to say this has changed and he is a lot better. In April they started the wonder drug and for the first 4 months we saw no real improvement but then it was increased to nearly double the dose and we have witnessed a new boy. He is a lot more confident and happy and can physically do things. Don't get me wrong his health issues still affect his daily activities and the rest of the family but he is 100% on last year.
During the first 2 weeks of January we went on a family holiday to Merimbula. Ethan had a ball. We took his bike which he loved riding everywhere. He rode it whenever he got the chance. He loved hooning around the caravan park on it. He cracked the sads at the Bermagui mountain bike trail because I wouldn't let him go with Luke on the big trail. He argued black and blue he could do it and sped off down the track! He even rode to Pambula and back, a total of 17km with me jogging and pushing him up the hills but he did it. (This time last year he couldn't even walk to the letterbox and back). He also loved going swimming, driving the boat and playing cricket.
Hope you enjoy the holiday photos. We will post birthday pics next week
During the first 2 weeks of January we went on a family holiday to Merimbula. Ethan had a ball. We took his bike which he loved riding everywhere. He rode it whenever he got the chance. He loved hooning around the caravan park on it. He cracked the sads at the Bermagui mountain bike trail because I wouldn't let him go with Luke on the big trail. He argued black and blue he could do it and sped off down the track! He even rode to Pambula and back, a total of 17km with me jogging and pushing him up the hills but he did it. (This time last year he couldn't even walk to the letterbox and back). He also loved going swimming, driving the boat and playing cricket.
Hope you enjoy the holiday photos. We will post birthday pics next week
Monday, December 29, 2008
Christmas and the last couple of months
In November Ethan took part in Aunty Mons wedding. The lead up was long and I wasn't sure if he would do it. One minute he was excited and the next he was over the fuss and was saying he wasn't going to take part in the stupid wedding! The day came and he was great. He was very well behaved and neat all day. My only concern was the photos, he loves to pull faces but we managed some great shots and the day was enjoyed by all.
The last few weeks of school were a nightmare. Ethan struggled and the school made quite a lot of phone calls to me. Ethan was struggling but not the usual physical exhaustion he was having trouble concentrating. The lights were on but nobody's home sort of stuff and he was very precious. He was asking to come home a lot and for the school nurse. His oxygen saturations were good but nurse Heather noticed his heart rate was jumping up and down. It wasn't long before he had a 24 hour cardiac monitor on, a follow up cardiac appointment and a walking test. The outcome being we can't do anything about the heart rate stuff, or the vagueness. This is hard to deal with. If he is struggling physically we can take over but we can't think for him. I hope this doesn't get worse. Sometimes he is on the ball and at other times he is as dopey as they come. The walking test was him walking as fast as he can for 6 minutes. He managed 235 meters. Pretty poor but before sildenafil he couldn't do that!
He also had a respiratory appointment to see what they thought. The chest x ray was the best ever! A heart the size of pharlaps and some clips from heart surgery but the lungs were clear. This was a shock I've never heard those words!! Dr David questioned whether his vagueness is from lack of sleep. He takes forever to fall asleep and is constantly up during the night and then I have to wake him bright and early for the bus. So he is on a sleep chart for 2 weeks. Not the best 2 weeks, he has had late nights non stop and hasn't been to bed at bed time once!!
Ethan's school report surprised me. I had to read it aloud to Luke to see if I was reading it right. Ethan sings the national anthem and the Glenallen school song at the primary school assembly in front of everyone. He is very confident when he's not vague! He is also very confident in the pool apparently..
Ethan is mad about cricket at the moment. He is always wanting to play in the backyard. Lucky for me the girls also like playing so once I've bowled them out and smashed them for 6 I can come back inside and leave them to it!! He is also right into football. The once devoted Kangaroo supporter seems to have jumped ship a few times and is flying the Bombers flag. He loves singing the team songs.
Suited up
More suits
The fam all scrubbed up
Skater boy
Kids happy the tree is now decorated
The Millenium Falcon
Lightsaber kit
Taking out Adam with the new lightsaber
At Nana Hanna's with new cousin Thomas on Christmas Night
The last few weeks of school were a nightmare. Ethan struggled and the school made quite a lot of phone calls to me. Ethan was struggling but not the usual physical exhaustion he was having trouble concentrating. The lights were on but nobody's home sort of stuff and he was very precious. He was asking to come home a lot and for the school nurse. His oxygen saturations were good but nurse Heather noticed his heart rate was jumping up and down. It wasn't long before he had a 24 hour cardiac monitor on, a follow up cardiac appointment and a walking test. The outcome being we can't do anything about the heart rate stuff, or the vagueness. This is hard to deal with. If he is struggling physically we can take over but we can't think for him. I hope this doesn't get worse. Sometimes he is on the ball and at other times he is as dopey as they come. The walking test was him walking as fast as he can for 6 minutes. He managed 235 meters. Pretty poor but before sildenafil he couldn't do that!
He also had a respiratory appointment to see what they thought. The chest x ray was the best ever! A heart the size of pharlaps and some clips from heart surgery but the lungs were clear. This was a shock I've never heard those words!! Dr David questioned whether his vagueness is from lack of sleep. He takes forever to fall asleep and is constantly up during the night and then I have to wake him bright and early for the bus. So he is on a sleep chart for 2 weeks. Not the best 2 weeks, he has had late nights non stop and hasn't been to bed at bed time once!!
Ethan's school report surprised me. I had to read it aloud to Luke to see if I was reading it right. Ethan sings the national anthem and the Glenallen school song at the primary school assembly in front of everyone. He is very confident when he's not vague! He is also very confident in the pool apparently..
Ethan is mad about cricket at the moment. He is always wanting to play in the backyard. Lucky for me the girls also like playing so once I've bowled them out and smashed them for 6 I can come back inside and leave them to it!! He is also right into football. The once devoted Kangaroo supporter seems to have jumped ship a few times and is flying the Bombers flag. He loves singing the team songs.
Suited up
More suits
The fam all scrubbed up
Skater boy
Kids happy the tree is now decorated
The Millenium Falcon
Lightsaber kit
Taking out Adam with the new lightsaber
At Nana Hanna's with new cousin Thomas on Christmas Night
Tuesday, October 28, 2008
The last 2 months
So much has happened over the last 2 months trying to remember it all will be hard.
EastLink: Everybody knows Ethan has a deep fascination with EastLink. He watches the making of EastLink DVD on repeat, he reinacts travelling on EastLink in his play, he has posters and pictures etc. Seeing his reaction to having a personalised tour of EastLink was amazing. He rode in the emergency response vehicle in both directions through the tunnels and over bridges before heading to the control centre. The team organised it very well, altering speed limits and blocking lanes while he was on the road and then allowing Eth to do the same when he was in the control centre. He had a great day. We would like to thank Glenallen and ConnectEast for organising the wonderful suprise.
School Camp: Ethan was also able to attend school camp. Jennifer and the staff at Glenallen took the class to Rosebud for 3 nights. They did lots of fun things but the most exciting thing for Ethan was the ferry trip to Queenscliffe. He was very excited that the boat could take cars on it. He had a great time being away but I struggled. I felt extremely gulity that I was relaxing and enjoying the break. Ethan has been away before but always at the same time as the girls. So having them home and Ethan not around was a reminder of how its going to end up. Very hard few days.
Respiratory Appointment: All went well at Ethan's follow up respiratory appointment. It's the best David has seen and we are going to try and reduce antibiotic cover and asthma medication over the summer months. With saying that Ethan was very disappointed he wasn't being admitted. Ethan has only just started coughing today. 2 months after his last admission; thats the longest dry period for years!
GP: When all is going well something has to pop up. Ethan had a major plantar wart on his foot. He couldn't walk. It was decided (after many discussions) despite poor circulation and the high risk of infection the GP would have to burn it off. It's been a while since I had to physically restrain Eth for a medical procedure and for a little weed he can be quite strong for about a minute until he's blue and looks like he's going to pass out. The bulk of it has gone but we have to go back and do it all again!
Cardiac: Ethan had his cardiac appointment last week. This is the first one since starting on the diuretics and increasing the sildenafil dose. The cardiologists were very pleased. Their "educated guess work" had paid off. They were extremely happy to hear the cyanotic episodes and chest pain had eased a lot especially during meals (meaning he can now eat without constant chest pain) He has put on a little bit of weight and is holding his own luckily. The dietician at monash will follow this more closely when we have our next tune up but it looks like he won't be needing a tube. They are planning follow up appointments with the cardiologist at monash when Ethan is admitted for his chest tune ups and with them again in a year. When questioned about whether that meant he'd be fine for a year with no deterioration they said they couldn't say. "We can't give time frames, today he is good and if he does deteriorate come back earlier". Ethan was even more disappointed he wasn't allowed to stay. He asked Geoff he could sleep in the new hospital for his 10th birthday, that was after yelling "wake up Geoff" and killing him with his light sabre!
Australian Hearing: Ethan had his hearing tested today. There has been no change since July. So at this stage there is no need for a hearing aid on the right side but we do have to make an appointment with the ENT surgeon to have a look in his ears.
Camp Quality: All of the kids got to go on junior camp last weekend. They did a lot of activities including fishing, going on puffing billy, seeing the Thomas show, Music shows, trampolining, flying fox, ball games. You name it they did it. When we arrived to pick them up Ethan pretended he didn't see us as it was nearly his turn on the trampoline! He had heaps of energy all weekend which was great to hear. All of the kids had an amazing time and have cried many tears as they miss their camp buddies!!
Photos to come.....
EastLink: Everybody knows Ethan has a deep fascination with EastLink. He watches the making of EastLink DVD on repeat, he reinacts travelling on EastLink in his play, he has posters and pictures etc. Seeing his reaction to having a personalised tour of EastLink was amazing. He rode in the emergency response vehicle in both directions through the tunnels and over bridges before heading to the control centre. The team organised it very well, altering speed limits and blocking lanes while he was on the road and then allowing Eth to do the same when he was in the control centre. He had a great day. We would like to thank Glenallen and ConnectEast for organising the wonderful suprise.
School Camp: Ethan was also able to attend school camp. Jennifer and the staff at Glenallen took the class to Rosebud for 3 nights. They did lots of fun things but the most exciting thing for Ethan was the ferry trip to Queenscliffe. He was very excited that the boat could take cars on it. He had a great time being away but I struggled. I felt extremely gulity that I was relaxing and enjoying the break. Ethan has been away before but always at the same time as the girls. So having them home and Ethan not around was a reminder of how its going to end up. Very hard few days.
Respiratory Appointment: All went well at Ethan's follow up respiratory appointment. It's the best David has seen and we are going to try and reduce antibiotic cover and asthma medication over the summer months. With saying that Ethan was very disappointed he wasn't being admitted. Ethan has only just started coughing today. 2 months after his last admission; thats the longest dry period for years!
GP: When all is going well something has to pop up. Ethan had a major plantar wart on his foot. He couldn't walk. It was decided (after many discussions) despite poor circulation and the high risk of infection the GP would have to burn it off. It's been a while since I had to physically restrain Eth for a medical procedure and for a little weed he can be quite strong for about a minute until he's blue and looks like he's going to pass out. The bulk of it has gone but we have to go back and do it all again!
Cardiac: Ethan had his cardiac appointment last week. This is the first one since starting on the diuretics and increasing the sildenafil dose. The cardiologists were very pleased. Their "educated guess work" had paid off. They were extremely happy to hear the cyanotic episodes and chest pain had eased a lot especially during meals (meaning he can now eat without constant chest pain) He has put on a little bit of weight and is holding his own luckily. The dietician at monash will follow this more closely when we have our next tune up but it looks like he won't be needing a tube. They are planning follow up appointments with the cardiologist at monash when Ethan is admitted for his chest tune ups and with them again in a year. When questioned about whether that meant he'd be fine for a year with no deterioration they said they couldn't say. "We can't give time frames, today he is good and if he does deteriorate come back earlier". Ethan was even more disappointed he wasn't allowed to stay. He asked Geoff he could sleep in the new hospital for his 10th birthday, that was after yelling "wake up Geoff" and killing him with his light sabre!
Australian Hearing: Ethan had his hearing tested today. There has been no change since July. So at this stage there is no need for a hearing aid on the right side but we do have to make an appointment with the ENT surgeon to have a look in his ears.
Camp Quality: All of the kids got to go on junior camp last weekend. They did a lot of activities including fishing, going on puffing billy, seeing the Thomas show, Music shows, trampolining, flying fox, ball games. You name it they did it. When we arrived to pick them up Ethan pretended he didn't see us as it was nearly his turn on the trampoline! He had heaps of energy all weekend which was great to hear. All of the kids had an amazing time and have cried many tears as they miss their camp buddies!!
Photos to come.....
Thursday, August 28, 2008
Day 400
Ethan will be coming home tomorrow after a very ordinary admission. I have done nothing but complain and whine for the last 2 weeks. We have had a lot of issues regarding bed time. I think he waves us of happily so he can get up and play. He has the staff wrapped around his little finger and gets away with murder even at midnight! We have also had major issues with his diet. Ethan is on a high calorie, thickened fluid diet as he has weight issues and aspiration issues so when the wrong meals come that have skinny everything and drinks that aren't thickened I get pretty pissed. I had nurses, food monitors, dieticians, PSA's, doctors and the charge nurse all involved in my anger!! Not sure if I'll ever get reemployed there!!! These issues come at a time when Ethan is at an all time low with his weight to age ratio. We have strict guidelines to follow to facilitate weight gain. If it doesn't go our way he will need to have a nasogastric tube inserted and supplements given either continuously overnight or top up feeds during the day.
Tomorrow is Ethan's 400th inpatient day. No wonder he is so confident there! Just as important it is Erin and Adele's 400th day too. They have had a horrible 2 weeks and both of them are out of sorts. I have warned them about Ethans weight. Adele is not too fussed, knows about the tube, has seen photos of Ethan with one from chemo days but is pretty laid back. Ez on the other hand is terrified. She can remember seeing it in his nose and out is mouth during episodes of vomiting after chemo, and me sitting on him to put it back in etc. Hopefully we can get him to eat lots of fatty stuff and it's not needed.
Tomorrow is Ethan's 400th inpatient day. No wonder he is so confident there! Just as important it is Erin and Adele's 400th day too. They have had a horrible 2 weeks and both of them are out of sorts. I have warned them about Ethans weight. Adele is not too fussed, knows about the tube, has seen photos of Ethan with one from chemo days but is pretty laid back. Ez on the other hand is terrified. She can remember seeing it in his nose and out is mouth during episodes of vomiting after chemo, and me sitting on him to put it back in etc. Hopefully we can get him to eat lots of fatty stuff and it's not needed.
Monday, August 25, 2008
August Ceftriaxone
Ethan was admitted to Monash last Monday for a chest tune up. This includes the usual IV antibiotics and physio. We were hoping it would be for a week and we would be home today but we are now looking at discharge on Friday. He settled in well and is running the place in true Ethan style. He is very comfortable there. He gives all the staff a high 5 goodnight and waves us off happily.
The IV came out today and had to be resited. He rode the bike into the treatment room, told the doctor how and where he would like the IV inserted and watched to make sure he was doing it properly. Not many 6 year olds would do that! He has also started doing his own medication. The nurses bring it in and he takes control putting in the IV bung and pushing it. He told me the other day he was going to be a nurse!! I'm not too sure what happened to driving the Ghan......
The physiotherapist has been using the vest during physio with good results. This takes some pressure of him when his heart doesn't allow him to participate.
The IV came out today and had to be resited. He rode the bike into the treatment room, told the doctor how and where he would like the IV inserted and watched to make sure he was doing it properly. Not many 6 year olds would do that! He has also started doing his own medication. The nurses bring it in and he takes control putting in the IV bung and pushing it. He told me the other day he was going to be a nurse!! I'm not too sure what happened to driving the Ghan......
The physiotherapist has been using the vest during physio with good results. This takes some pressure of him when his heart doesn't allow him to participate.
Sunday, August 17, 2008
Wednesday, July 30, 2008
Wednesday, July 16, 2008
the last 6 weeks
So much has happened in the last 6 weeks.
A couple of days after Ethan was discharged he was having the odd fever and was very blue and lethargic. I tried to speak to the respiratory doc, paediatrician, and cardiologist but they were all out of the office. I tossed up the idea of calling the respiratory docs mobile number (which i had stored in my mobile from a previous occassion) I didn't want to harrass him on a day off but I needed to speak to someone so I called. The receptionist should have said he was over seas not out of the office. 3am his time he still managed to organise scans and follow up at monash for us. I felt bad but atleast we got results that his chest wasn't any worse and we could continue on at home.
We were lucky enough to be given tickets to the V8 supercars at Sandown. We were even luckier to see pit lane, the garage, sit in the car, see the truck and get some merchandise. It was just like the pixar movie cars. Ethan loved it. In Dr David's words, "He is such a petrol head!" This was followed with Ethan and Adele attending junior camp. They both had a ball with the many activities organised for them. Ethan loved telling us about the bus trip there, the bridges and the new roads he went on! It was good to see them happy after spending a couple of tiring weeks at monash. We would like to thank Challenge for providing us with these great experiences.
Ethan has also been very excited as Eastlink has opened. After watching it progress every day on the bus he finally got to go on it. He doesn't stop talking about it, looking at posters of it and watching a DVD about it. Glenallen organised the posters and DVD as he wouldn't stop talking about it at school. In news group he would announce how many days to the opening etc. Glenallen are also organising for him to go in the Eastlink patrol vehicle and command centre. He knows all of the bridges and off ramps, he especially loves the monash/eastlink interchange. He plays eastlink on the posters (some are laminated) and makes the bridges with his train tracks. We have threatened to take his posters off him when he is naughty, he soon behaves!
During the school holidays we went to Mt Baw Baw for 4 days. We have wanted to go in the past but I've always opted to holiday in the sunny places as Ethan doesn't tolerate being cold and he manages to look even bluer than usual. I rugged him up like an eskimo and off we went. It is the first time Ethan has been quiet in the car, he went from blue to green! Luckily he didn't vomit just felt car sick. It is the first family holiday we've been on where Ethan has not become acutely unwell. Amazing!! The kids had a ball. Ethan didn't like the wind or the snow hitting his face but loved playing in the fresh snow while the sun was out. He loved tobogganing on the gentle slope but wasn't a fan of the faster hill or crashing! Overall he had a good few days.
Medically Ethan has had a few appointments.
Oncology appointment went well. All scans are clear. Dr Peter is happy with his progress and doesn't believe the cancer will come back.
Radiation oncology appointment also went well. There are no signs that the radiation has caused growth issues within his spine, or problems with his bowel and bladder, and it hasn't caused any other tumurs, all good.
Respiratory appointment went as good as it could. Ethan was in fine form asking Dr David to give him 5, in the city, pinch your titty! He was also showing off with the homer dance and calling everyone losers especially the medical students! Ethan is now rotating between augmentin duo and keflex. We need to go back in 2 months if we are not admitted before this. We left with the usual goodbye; see you on the ward in a few weeks. While we were at the respiratory appointment we saw physio. Narelle had managed to secure herself the new vest device so she hooked him up and away it went. The vest fills with air and shakes his chest making physio a lot easier and less strenuous. It was great. Ethan was nervous about it but soon realised it was fine. During our next admission we will get to play with it a bit more and if it doesn't interfer with cardiac blood flow we will hopefully trial one at home.
Ethan also had his Cardiac appointment. He had the usual scans and discussions and as a result the sildenafil has been increased and will get increased again in a week. We are doing this at home without monitoring so it's been a little scarey. So far so good. He has also started on 2 diuretics to help ease some puffiness and ease pressure from his heart. These seem to be helping at the moment.
Photos to follow
A couple of days after Ethan was discharged he was having the odd fever and was very blue and lethargic. I tried to speak to the respiratory doc, paediatrician, and cardiologist but they were all out of the office. I tossed up the idea of calling the respiratory docs mobile number (which i had stored in my mobile from a previous occassion) I didn't want to harrass him on a day off but I needed to speak to someone so I called. The receptionist should have said he was over seas not out of the office. 3am his time he still managed to organise scans and follow up at monash for us. I felt bad but atleast we got results that his chest wasn't any worse and we could continue on at home.
We were lucky enough to be given tickets to the V8 supercars at Sandown. We were even luckier to see pit lane, the garage, sit in the car, see the truck and get some merchandise. It was just like the pixar movie cars. Ethan loved it. In Dr David's words, "He is such a petrol head!" This was followed with Ethan and Adele attending junior camp. They both had a ball with the many activities organised for them. Ethan loved telling us about the bus trip there, the bridges and the new roads he went on! It was good to see them happy after spending a couple of tiring weeks at monash. We would like to thank Challenge for providing us with these great experiences.
Ethan has also been very excited as Eastlink has opened. After watching it progress every day on the bus he finally got to go on it. He doesn't stop talking about it, looking at posters of it and watching a DVD about it. Glenallen organised the posters and DVD as he wouldn't stop talking about it at school. In news group he would announce how many days to the opening etc. Glenallen are also organising for him to go in the Eastlink patrol vehicle and command centre. He knows all of the bridges and off ramps, he especially loves the monash/eastlink interchange. He plays eastlink on the posters (some are laminated) and makes the bridges with his train tracks. We have threatened to take his posters off him when he is naughty, he soon behaves!
During the school holidays we went to Mt Baw Baw for 4 days. We have wanted to go in the past but I've always opted to holiday in the sunny places as Ethan doesn't tolerate being cold and he manages to look even bluer than usual. I rugged him up like an eskimo and off we went. It is the first time Ethan has been quiet in the car, he went from blue to green! Luckily he didn't vomit just felt car sick. It is the first family holiday we've been on where Ethan has not become acutely unwell. Amazing!! The kids had a ball. Ethan didn't like the wind or the snow hitting his face but loved playing in the fresh snow while the sun was out. He loved tobogganing on the gentle slope but wasn't a fan of the faster hill or crashing! Overall he had a good few days.
Medically Ethan has had a few appointments.
Oncology appointment went well. All scans are clear. Dr Peter is happy with his progress and doesn't believe the cancer will come back.
Radiation oncology appointment also went well. There are no signs that the radiation has caused growth issues within his spine, or problems with his bowel and bladder, and it hasn't caused any other tumurs, all good.
Respiratory appointment went as good as it could. Ethan was in fine form asking Dr David to give him 5, in the city, pinch your titty! He was also showing off with the homer dance and calling everyone losers especially the medical students! Ethan is now rotating between augmentin duo and keflex. We need to go back in 2 months if we are not admitted before this. We left with the usual goodbye; see you on the ward in a few weeks. While we were at the respiratory appointment we saw physio. Narelle had managed to secure herself the new vest device so she hooked him up and away it went. The vest fills with air and shakes his chest making physio a lot easier and less strenuous. It was great. Ethan was nervous about it but soon realised it was fine. During our next admission we will get to play with it a bit more and if it doesn't interfer with cardiac blood flow we will hopefully trial one at home.
Ethan also had his Cardiac appointment. He had the usual scans and discussions and as a result the sildenafil has been increased and will get increased again in a week. We are doing this at home without monitoring so it's been a little scarey. So far so good. He has also started on 2 diuretics to help ease some puffiness and ease pressure from his heart. These seem to be helping at the moment.
Photos to follow
Sunday, June 08, 2008
Home again
The week of antibiotics turned in to 12 days. I should have realised a week was not enough as it is usually ten days at least. While Ethan was admitted they continued antibiotics and physiotherapy. Ethan is finding the physio sessions harder as his heart doesn't allow him to be as active. He had a major episode during physio where he went very cyanotic; extremely blue and very short of breath. It scared the hell out of the physio and the staff around. He usually stops prior to that happening. They are trying to get their hands on some new whizz bang thing which allows him to be passive but moves his chest and makes him cough but it all comes down to budget. The physiotherapists are great with him. He has a couple of favourites but he loves Narelle the best, "I love Narelle". Overall he enjoys physio but sometimes its a real battle especially if he is feeling a little off prior to starting. The plan is to stay on antibiotics for 6 weeks until our follow up appointment, the usual regime of home physio and oxygen as needed. The sildenafil has been increased but there is still room to increase it again which will most likely happen during our next admission. Overall his oxygen saturations can range from 70-80% when sitting still, 60-70% with a chest infection and when he is active they are too low for the machine to detect. They drop during the everyday activities like dressing and eating. The eating seems to be the big issue. He goes blue and grabs at his chest a fair bit. It can be pretty scarey. Overall his cyanosis is getting worse and comes on quicker. We have a cardiac appointment in a about a month which we will be discussing ways to manage this.
We are all happy to be home except Ethan who has already asked to go back!
We are all happy to be home except Ethan who has already asked to go back!
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