Tuesday, December 29, 2009

Update 29/12/09

Hi everyone,

We hope you all had a great Christmas!

Just before Christmas we got the fabulous news that Tim's biopsy result was clear of leukemia and in fact there was evidence of new, healthy cell rejuvenation. So needless to say, we were all very relieved and Tim celebrated with a beer on Christmas day!
( and me with a number of sparklings!)

We had a lovely holiday in Noosa with the kids and arrived back in Melbourne just before Christmas. However we did have a scare from the hospital just as we were at the airport and about to start our holiday. Tim had to have a PICC line redress and blood tests the morning of our flight, which are routine and weekly. However the hospital called to say Tim's neutrophils had dropped and the haem. doctors were very concerned by this. Great...what were we going to do....yep that's right, still go on the holiday! We did have a great time but of course had some worry in the back of our minds (actually it was at the front of mine). So while trying to enjoy the sun, fun and family time, we had many calls from doctors to organise an emergency bone marrow biopsy 12 hours after our return. One doctor did say that his low neutrophils could be an indication of leukemia cells reforming and inhibiting healthy cells. I actually overheard her say that to Tim on the phone, whilst lazing by the pool. Straight away i had that kick in the guts feeling and the shakes. Tim immediately called the Head of Haematology, Dr Paul Turner for some clarification. Dr Turner assured Tim by saying that if he was him he wouldn't worry and that the drop in counts could be due to a very small sniffle he had at the time and when your bone marrow is so suppressed the drops are more dramatic. However, he felt also that it would be good for everyone to have another bone marrow biopsy to make sure. So this, along with Tim's insistence that there is no way he could be feeling this good if leukemic cells were forming in his bone marrow and that fact that he looks a million bucks, we had a great time away and just immersed ourselves in the quality family time. We are blessed to have enjoyed this Christmas. We are reminded constantly of how quickly things can change with this disease, for better and worse. Unfortunately some of our friends from the Gawler retreat have not had great news since the program.

Tim is having another dose of chemo this wednesday (IV and another delightful lumber puncture) which will flaten him for New Year celebrations no doubt. The good news is that this week was supposed to be a 5 day chemo week, but the haem. doctors have decided that one dose is enough. The plan is that this dose is repeated again in 4-5 weeks and then the blessed PICC line is removed!!! HOORAY! Everything is crossed for that going to plan. This means that Tim will have daily chemo in tablet form and 8 weekly lumbar punctures for the following 2 years.

Tim is going to do the 8 week Integration Program run by the Gawler Foundation in Melbourne starting the 8th Feb. This time his dad is going as the support person, as I am returning to work next year. It is a 3 hour session held once a week in Hawthorn run by the Zen Monk, Seikan. I am sure they will both gain so much from the program.

It is certainly a way of life now...to juice, meditate and eat well. We have found a routine that suits us and it is really working well.

We wish everyone all our best for a good new year. Tim and I continue to focus solely on each moment and really live them.

Love and peace,

Andi & Tim

Extra Update 29/12/09 @ 6pm

We had a call from the hospital today and Tim will not be having chemo tomorrow, but will recommence on Monday the 4th. Unfortunately, he will have to have the 5 days of chemo as originally intended.

Tuesday, December 8, 2009

Update 8/12/09

Hi all,

We are travelling well at the moment. Tim is continually being told how well he is looking. The diet and meditation having a massive impact!

Enjoy the recipes below. Tim actually made the crumbed tofu himself! YAY! (& the coleslaw!)

Love Andi

Marinated Tofu with Rice Vermichelli noodles
(Andi's recipe)

I block of Tofu, cubed (3cm)
I clove garlic
1/3 cup tamari
1 tbs honey

1 bunch bok choy
1 carrot chopped
1 large mushroom chopped
1 bunch broccoli
3 spring onions
1/2 cup organic roasted cashews

1 pkt Rice Vermichelli Noodles

Marinate the tofu in tamari, garlic and honey for 1/2 an hour. Place tofu and marinade in a pan with the chopped white ends of the onions. Add carrots, then broccoli, mushrooms, bok choy and cashews and then add a little water (about 1/4 cup) and cook till veggies are tender.

Cover the noodles with boiling water till cooked (about 3-4 minutes). Drain and serve adding the tofu and vegetables on top. Sprinkle with some remaining spring onions.

Crumbed Tofu

500g Tofu cubed (3cm)
1 cup tomato juice
1/4 cup tamari
1/2 cup finely chopped spring onions
2 cups fresh bread crumbs

Mix tomato juice,tamari and spring onions. Marinate tofu cubes for 1 hour. Coat in bread crumbs and cook in moderate oven for about 20 mins.

Serve with a salad. (We do coleslaw or potato salad)

ps. Kids eat these like chicken nuggets!


Coleslaw

1/4 cabbage, finely shredded
1/4 red cabbage, finely shredded
1 large carrot, grated
1 cup finely sliced spring onions
2-3 tbs soy mayonnaise

Mix all ingredients in a large bowl and serve!

Sunday, November 29, 2009

Update 29/11/09

Hi all,

Not too much to report at the moment. Tim is having a break from treatment and enjoying it! He still has to front up to day oncology once a week for a PICC line redress and bloods, which are all on the way up at the moment. We are hopeful that chemo will recommence after Christmas, so that we can enjoy some family time away up north and also enjoy the festive season with our family and friends.

Many have asked us for a few recipes that we enjoy from the Gawler Foundation, so please find a few below. I will try and add a couple to each update.

Also, a BIG thank you to the mystery person, who organised for a box of delicious organic fruit, veg and tea to be delivered to our door from 'Organic Angels'. The produce was just top quality and we are very grateful to who ever it was...(hopefully you read this!)

Love Andi xxoo.

MUESLI

1 cup barley flakes
1 cup rolled rye flakes
1 cup rolled oats
1 cup sultanas or currants
1 cup chopped almonds (bio dynamic)

Pour desired amount in to bowl, then soak the muesli for 2-3 minutes in apple juice ( we use Greenwoods bio dynamic)
Top with milk (Tim has oat milk) but soy or rice can be used too.
Dollop some soy yogurt on top and dust with some cinnamon

BROCCOLI & ALMOND SOUP

4 cups broccoli roughly chopped
1 onion chopped
2 tbs almonds chopped
4 cups water
1/2 cup soy milk
1 vegetable stock cube (or 1 tsp mineral bouillon)

Place onion in pan with water and bring to boil then add broccoli. Cook till soft. Add stock cube and soy milk. Puree. Add almonds just before serving.

RICE PAPER SALAD ROLLS

12 sheets rice paper
6 cups shredded cabbage (red or green)
1 cup fresh mint
1/2 cup french dressing (fat free)
4 cups shredded lettuce
2 cups red capsicum,julienned
2 cups snow peas
alfalfa sprouts
150g tofu

Cut tofu in 12 strips and marinate in 1/2 cup of Tamari (soy sauce) and 1/2 cup of water for 30 mins. Lightly steam cabbage, rinse and cool, then add dressing and mint. Individually, soak the rice paper sheets in warm water till pliable then place on a clean tea towel. Add 1/12 of each ingredient in the centre and roll up, tucking the ends in as you roll. Work one roll at a time.

Fillings may vary and the rolls may be served with a dipping sauce.

ROAST VEGETABLE RISOTTO (Andi's recipe!)

1 cup bio dynamic brown rice
3 cups water
1 zucchini
1 carrot
2 roma tomatoes
1 large mushroom
1 red onion
splash of balsamic vinegar
pinch sea salt
black pepper
grated parmesan

Place rice and water in pan and cook by absorption method. (approx 30 - 45 minutes)
Meanwhile chop all veggies into small cubes, place in an oven dish, splash with vinegar, salt & pepper and bake in oven 150 degrees (fan forced). When carrots are cooked, add vegetables and juice to the rice, mix in some grated parmesan and serve!


BONN APPETITE EVERYONE! ( and also, in all recipes above we use organic produce where possible)

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From the Admin:

Howdy all! Just a quick bit of boring blog management - currently the 'donate now' button on the right works by sending the amount you donate through to paypal and then on to an account that was set up for Tim and Andi to use. I've been letting these payments go through to them anonymously, but Andi has now asked for details when someone donates so she and Tim and thank whoever was feeling generous. She can't help herself!
So, if you do donate and want it to be anonymous, just send an email to the administrator - thehamiltonfamilyblog@gmail.com - letting me know and I'll send the payment through anonymously as I've been doing, otherwise I'll let Tim and Andi know who you are!

Thursday, November 12, 2009

Update 12/11/09

Hi everyone,

We are now home from our ten day retreat at Ian Gawler's Yarra Valley Living Centre. We are refreshed, energised, well informed and......almost vegan! Each day was jam packed full of interesting and dynamic concepts, discussions and tutorials. Our days began at 7:45 am with meditation and ended in the same way at almost 9pm! In between was filled with tutorials covering all of the following topics; meditation, diet & nutrition, brain training, pain management, food preparation, causes of cancer, dynamic contemplation, cracking the medical code, living & dying, forgiveness, healing the past, healing & imagery, spirituality & healing, mind- body medicine, connections through voice and awareness through movement. It was extremely 'full on' and confronting, but at the same time so engaging and completely fascinating. As you can imagine, from all the information given to us, not only did we learn so much about cancer (causes, treatments, management & prevention) but also so much about ourselves. Luckily Tim and I have no problem being open and willing to share so much of ourselves. This enabled us to gain maximum benefit from all the group discussions and come to some massive realisations.

Other features of the residential program included yoga, deep relaxation, massage, yoga breathing, qigong ( tai chi), garden tours ( featuring a demonstration of constructing a 'no dig' vegetable garden) and of course the main focus meditation (which we were guided through several times a day).

The property is spectacular and we were so fortunate to have beautiful weather to stroll around the gardens and see the wildlife up close and personal, namely a mob of kangaroos, a couple of deer and the resident wombat and koala. The bird life was magical and everyday I spotted a bunny hopping across the lane. We really did feel like we had escaped the 'real world'. It is hard to believe that we survived 10 days without meat or any animal products, no tv, no newspapers, no alcohol, no caffeine and no children!!!!! Funnily enough we did it well.....however we did sneak in a phone call to the kids everyday!

We met wonderful people, from all the facilitators to the other sufferers and support people. There were 40 of us in total. Tim and I were the youngest after a lovely man from N.Z (aged 26) had to leave on day 4 as he was in severe pain. Like us, he too had two little boys, 3 and 15 months. Unfortunately his health was not good and we found out later that his terrible pain was in fact a spread to his jaw and shoulder. The group felt so sad to see him go, however it was obvious in the end that he needed urgent medical attention. Most of the participants were from interstate and N.Z and all at various stages with their disease, some currently cancer free, some with active cancer but under control, some palliative. The people were so friendly, happy and fun loving that at times you did forget that everyone was sick. But then a wig was removed and a painful grimace revealed to remind us of why we were all there....

So what will change in the lives of Mr. Tim and Andrea Hamilton??????

Firstly, would have to be the importance of finding the space and time everyday to still the mind through meditation. We have learnt that time put aside for this everyday has enormous benefits, especially for boosting the immune system, creating a natural balance within and giving the mind a rest. This deep stillness where the mind is free of reaction and free of judgement creates a clear mind, where stress levels decrease and good choices are more likely to be made.

Since living in the real world again, we have not been able to meditate as frequently as we had hoped ( which was twice a day) so once a day is a more realistic goal, given we have such a busy life with the children.

Secondly, is the importance of a nutritional wholefood diet. The diet at Gawler's is essentially vegan, with a few extra restrictions including salt, refined sugar and most oils ( except flaxseed and a tiny amount of olive oil). It is an incredibly restrictive diet, however, if your body is dealing with active cancer, there is a very good reason for it. Off the menu was beef, chicken, fish, eggs, butter or marg, black tea, coffee, yogurt, cream, cows milk ,cheese, alcohol and very little fruit. So really, what ate for 10 days was rolled oats, dark rye spelt flour bread, brown rice and pasta, vegetables and salads. Added to this was the vital part of the Gawler diet, being 7 fresh vegetable juices a day. The idea behind such a diet is to create a cancer unfriendly environment within the body. Cancer apparently feeds off fats and sugars, so it was made very important to us to have next to none in your diet when dealing with active cancer. Cancer is hindered by high cellular oxygen levels (which can be found in juices ), high potassium/low sodium levels ( bananas are good and no salt) and a high alkaline/ low acid balance ( caution with oranges and acid foods). Foods that have anti cancer properties include: (there are loads more) cabbage, pomegranate, raspberries, turmeric, tomato and broccoli, so it is important to add as many of these in as possible.

Tim found the diet very difficult to begin with, but I am very pleased to say having been home one week now, that he has maintained a very healthy diet and has maintained the dramatic changes that were made on the retreat. For the most part we intend to adopt a vegetable based, whole food diet, however we do intend to still eat a small amount of meat as long as it is not processed like some sausages and salami.

Tim starts the day now with an organic home made wholegrain muesli that includes rye flakes, rolled barley, rolled oats, almonds and sultanas with oat milk and a carrot juice. Lunch has varied from salad sandwiches on organic spelt rye bread to rice paper rolls to sushi to miso soup with a pomegranate juice and dinner usually a consists of a pasta, rice or noodle based dish with vegetables and/or tofu. These changes are big for Tim who prior to getting sick, had no breakfast, a coffee at 7.30am, a couple of dim sims at 10.30, lunch varied from a pie, sandwich or schnitzel burger, a couple of beers at knock off, home for dinner and then a couple more beers. I am so pleased to see Tim care for himself in such a healthier way and make these changes to ensure he gives himself the best opportunity to kick cancer for good.

We sincerely hope that you won't be too scared to invite us for a meal again!! We still feel it is important to live life and enjoy and indulge from time to time!

There is no doubt that our experience at Yarra Junction was life changing and has left a remarkable impression on us both. Dr Ian Gawler is truly inspirational, unique and the most disciplined human being I have ever encountered. He speaks with such honesty and insight that you feel compelled to record everything he says. It is no wonder he defied the odds to go on to live a long, healthy and enriching life. His positive, calm, intuitive and extremely determined persona is inspirational and a force to be reckoned with. Cancer had no chance with him and I am feeling very positive that Tim will find himself in a very similar position. Blood tests on Monday revealed a rise in all counts which really validates the integrated approach.

Tim has recommenced chemo this week and I am also very happy to let you all know that he has had another great bone marrow biopsy result!

Hope you like the photos below. The boys didn't miss us one little bit!!!!


Thursday, October 15, 2009

Update 15/10/09

Hi All,

Well, Tim has finally been able to resume treatment this week. This was after much discussion and a meeting between the oncologists and haematologists at the Austin, where it was decided that Tim would resume the treatment protocol, but the dosage of all the chemotherapy to be reduced by fifty percent. We have decided upon this strategy as a way of moving forward and receiving treatment. Otherwise, we were falling into the cycle of having one full dose of chemotherapy that was completely wiping out all cell production in his bone marrow and being unable to have treatment for several weeks. As you can imagine, it is has been a huge mental challenge for Tim, where the continual 'rejection' at Day Oncology has been depressing. We see this move as very positive, a) because it is a step closer to the end of the protocol and b) that he does have the 'luxury' of being a candidate for a reduction in chemo.

So, Tim recommenced yesterday, with two chemotherapy drugs (Cyclophosphamide and Cytarabine) administered through his PICC, three drugs ( methotrexate, cytarabine and dexamethasone) intrathecally (into the spine) and one drug (Thioguanine) orally. Just a nice way to ease him back into it all!!!! Boy oh Boy !! He is due to have cytarabine daily this week as well as the chemo tablets for 14 days straight, all at half the dose originally prescribed.

Tim, so far, has noticed that the side effects are only half as bad. This is great. Usually, after a full dose of what Tim had yesterday, he would be bed bound for a couple of weeks. But on the reduced dosage, he is able to sit up, with mild nausea and headaches. So this does seem a promising move forward.

We are counting down the days till Ian Gawler's Residential Life & Living Program. It will mean a short break in treatment, but the doctors at the Austin are very happy for Tim to go and compliment his medical treatment with the natural therapies offered. The two main focuses of the program will be meditation and diet and we are both so keen to participate and immerse ourselves in some natural healing. We will miss the kids like crazy, but see this as such a valuable opportunity. The kids know we are going to "Ian's" or "the man with one leg" to help daddy get better and they are extremely excited about all the time they will be spending with nanny and poppy and nanna and pa! I think we are all pretty lucky really!

So glad to finally have some news for you all.

Take care,

Love Andi

Wednesday, September 16, 2009

Update 16/09/09

Hi,

Still not a lot to report as Tim has not been able to progress any further with the protocol since my last update. His red and white blood counts are great, it is just his platelets that are only ever so slightly low, but this means he cannot have chemo. We were very surprised by this, as he looks and feels well....but whacha gunna do??!! ....Just go with the flow....... This particular round of chemo was only supposed to take four weeks....we are now at week 10 and it is not complete. It certainly looks as though the re induction phase, which we were hoping to be through with by early November, will work its way into the first few months of 2010.

When Tim has felt well, he has enjoyed getting out into the spring air and pottering in our garden. A small veggie patch which we have dreamt about doing for so long, has finally come to fruition.....only to be enjoyed even more so by Riley (GGgggrrrrrrr). Tim is doing a lot of meditation to still that racing mind of his. I am happy to say that it is working and he is looking more relaxed, but there is still often a moment when sheer frustration kicks in at the inability to lead a normal life. He misses his work, his friends, being spontaneous and also misses being able to plan ahead. The biggest realisation for us all has been the importance of focusing solely on the moment. It makes it so much easier to live.

Fingers crossed I have news of some progress for you all.

Love and smiles from us all,

Andi

Monday, September 7, 2009

Update 7/9/09

Apologies for the break since my last update. This is because Tim was
only able to resume chemotherapy last Tuesday as his blood counts have
been taking much longer to recover after chemo. Since my last update
Tim has had two blood transfusions and also a potassium infusion as
blood tests revealed a deficiency in this area. A potassium tablet
has been added to list of daily medications and so has prednisolone,
which is the drug that gives him a puffy face and an enormous
appetite.

Tim enjoyed his Fathers Day, the boys and I spoiled him with lots of
presents, kisses and cuddles. It was great that he felt well enough
to enjoy the day and some precious family time.

Looking ahead, Tim has chemo on Tuesday this week and then next week
begins daily IV chemo for 5 days straight and a lumbar puncture. A
break is scheduled after this to allow his body to recover.

Hope you enjoy the photos of Joshua's Fathers Day creations!

Love Andi


Friday, August 21, 2009

Update 21/08/09

Hi everyone,

Not too much news to report at the moment. Tim has been having weekly chemo, but unfortunately this week, was not able to have it as his blood counts were too low. We are only up to week 22 of the protocol, ( it has been 33 weeks since diagnoses) as we have had so many set backs, delays and inclusion of radio therapy. Week 24 sees the regime step it up a notch to intense daily chemo again and this will last till week 34 of the protocol. So really, Tim is just over the half way way mark of intense treatment. A very intense 3 months still to be had. According to the protocol Tim still has 110 weeks of treatment to go..........

Tim's hair is starting to grow back, at this stage we can't make out whether it is grey or blonde fluff.....but it is certainly not red! ( although his beard is!)

Should have more news next week as Tim and I are hopefully going to have a meeting/review with his haematologist and head oncologist. Even though the process is painfully slow, Tim is still making steady progress.

Bye for now,
love Andi

Monday, August 10, 2009

Update 10/08/09

Hi everyone,

Tim was able to recommence treatment last Thursday. This consisted of IV chemo on Thursday and a lumbar puncture (LP - chemo injected into his spine) on Friday. He said the familiar 'chemo feeling' came back straight away and he could feel the effects of it running through his body. The LP, as it has done so in the past, has knocked him out. The only relief from his throbbing head is to lie down, but when horizontal, he has pains in his back and legs. No win. Unfortunately, we have a long way to go with the LP's. They are integral to the maintenance phase of the treatment protocol, which is the next phase after this one. Tim will be having an LP every 8 weeks for 2 years when the maintenance phase begins....we hope this will be in November. The LP's are so vital as they are to prevent a spread or relapse to the CNS (central nervous system). Apparently, the CNS can be a 'hot spot' for relapse. Tim was fortunate that there was no involvement with the CNS when he was first diagnosed. Seeing Tim struggle with his symptoms has been hard. Tim and I discussed this morning, how on earth could a child cope with all this? Knowing that his disease is more commonly found in children, gives us some perspective and some extra courage.

I have been finding it all very hard to cope with lately. I am tired, sick and tired, tired and sad, over it. The best thing I did was have a good day of crying last Sunday...yep in front of the kids too. It seems to have lightened a load. Also, highlighted the power of positive thinking. I believe that is the key.

Strangely, it has been a good thing for us all, to have Tim back on track with treatment. It gives us all a focus. Makes the light at the end of the very long tunnel, a little brighter.

That's it for now........oh, except Tim did shave off that feral beard!!! Yay!

Love Andi

Monday, August 3, 2009

Update 3/8/09

Hi everyone,

After 7 nights in hospital, Tim was able to leave but unfortunately not come home. As the boys and I were sick, Tim had to spend another 4 nights at my parents home until we were on the improve. It has been a very difficult time and even though Tim is now home, he is in the worst shape he has ever been. He is suffering constant nausea, head aches, dizziness (has almost fainted on me!) leg pain, stomach cramps....the list goes on. He has no energy and has finally lost his spark. It has been very hard/sad/devastating for me to see him like this......not even an attempt at a bad joke!! His spirits lifted slightly when finally allowed to see his children and also when he layed eyes on his beard. Doctors are baffled by his poor disposition as his blood counts are all up and rising..on paper he is ready to move on to the next phase of treatment. On Tuesday he will be reassessed. If there is no improvement in his well being he will be readmitted for observations and if he does improve he will recommence chemo this Thursday.

I have found an excellent medical website that examines Tim's exact condition. It also discusses and clarifies the dilemma over whether Tim has lymphoma or leukemia. As you will read, the World Health Organisation recently unified the disease as T cell lymphoblastic lymphoma/leukemia. This has helped us to understand why some doctors refer to Tim as having leukemia.

Please take the time to read the complete study: Background, Diagnoses, Treatment & Follow up. It is accurate, up to date and informative.

http://emedicine.medscape.com/article/203556-overview


Love Andi.

Friday, July 24, 2009

Update 24/7/09

Hi everyone,

We have had a set back..... Tim is back in hospital. Tim presented a slight temperature when having his routine PICC line redress on Tuesday. Doctors were concerned by this and ordered immediate blood tests and cultures. Unfortunately, Tim's neutrophils had dropped again and he has become neutropenic. Blood culture test results have indicated an infection in his body and it looks as though the infection is primarily in is in his PICC line. This means that the PICC in his left arm will have to come out and a new one put into his right.

Tim is coping incredibly well with all this. So much easier to deal with when you have been through it all before. On admission to the ward on Tuesday night when the nurse asked if he wore hearing aids he responded with "what?" and is English your first language, he said "Si". MMMMmmmm. The nurse thought he was hilarious!!!!!! (Note the sarcasm!!)

More to come, no doubt.

Love Andi xx.

Friday, July 17, 2009

Update 17/07/09

Hi everyone,

We have had an action packed couple of weeks. All things going well at the moment which is so lovely. Last week was very exciting for Tim as he was able to attend Windy Hill to see Josh participate in a clinic run by the players. It was fabulous and cold and both boys in their element! (see photos below)

John and Barbara (Tim's parents) took us to meet Dr. Ian Gawler OAM, at his Yarra Valley Living Centre in Yarra Junction. It was an incredible day, we had a tour of the property and met with Ian for an hour. It was an amazing encounter where Tim, myself and his parents had the opportunity to share our feelings with Ian and each other. He certainly has a genuine, energising presence about him and I found his compassion and eagerness to listen......really listen, completely heart warming. We felt so fortunate to meet him and give thanks to John for making it all happen. For those of you who don't know John worked for Gawler Foundation some years ago and is a personal friend of Ian. People travel from all over the globe to meet Ian, so we are incredibly lucky. He is planning to retire in March and Tim and I are hoping to attend his Life and Living 10 day retreat later in the year. This retreat is a transformative lifestyle based program that helps to overcome the challenges of cancer. Look out everyone.....Tim may come out this cancer journey a Vegan!!! Check out www.gawler.org for any more info on Ian and the Gawler Foundation.

I am saving the best news now for last..and that is the bone marrow biopsy result.....................(
drum roll).............ALL CLEAR! We are thrilled! Of course this has given Tim a massive boost in spirit and confidence. We are making baby steps, but certainly they are forward, to recovery............YAY!!!!

Have a great week end. We are planning to too!!!

Love Andi.


Tuesday, July 7, 2009

Update 7/7/09

Hello everyone,

Tim is home now after a turbulent week of feeling ok one minute to not good at all the next. It has been difficult to adjust to every moment, as a sense of security and flash of wellness is completely turned upside down 20 mins later by a bout of nausea and all over body aches. My nerves have been on tender hooks as we have done our utmost to psych neutropenia away.......and I think we may have been successful!!!!

This week saw Tim admitted for a night on Monday. He had spent the week end at home, but unfortunately couldn't bring himself to be upright nor eat or drink anything as he felt extreme nausea. He was due into day oncology for blood tests and faced up in pretty bad shape (threw up 15 times) and the doctors decided he needed to be in o/n. After some strong anti nausea, IV fluids for 24 hours and a cell boosting injection (GCSF) he was good to come home again.

After two days of feeling ok, Tim woke on Thursday morning to find himself covered in bruises. Called the hospital and the next thing we knew he was in again having a platelet transfusion. His platelets tested at 13 which is extremely low ( platelets test at around 450 in a normal, healthy person). This is what had caused the bruising and it is scary to think that it was just normal toss and turn in his sleep that instigated the outbreak. If platelets test 10 or under, you are in danger of a spontaneous bleed. Luckily Tim is right on to everything and acts on his intuition. This has saved his life more than once in the last 6 months. (Sounds so dramatic, but is actually true!!!)

The up times this week have included some lovely family time at home, eating home cooked meals and watching numerous games of AFL. Tim was treated by Andrew and Harry Belli on Saturday night to the Crown Palladium for Essendon's 84/85 Premiership reunion dinner. It was so lovely to see him suit up and enjoy a fun and memorable night. I think he would have rolled up there attached to a drip, he was so determined to go!!! We were all so pleased that he could. It meant a great deal to Tim to be there.

Tim is now waiting for his blood counts to come back up, then he will begin the re induction phase of treatment. This is more or less a repeat of everything he has already had, minus the radiation and 24 hour chemo infusions. Yes, we are definitely making progress, but the next few months still involve daily chemotherapy.

Take care,

Love Andi
xoxoxoxo

ps. The scratch on Tim's nose below was caused from vomiting too many times into a sick bag. (just in case you were wondering!!!! ......chemo...it's a bloodsport!!)


Monday, June 29, 2009

Update 29/06/09

Hi All,

Tim is home. Not feeling too great at the moment, although he did muster up a smile for me for you (see below). Thought you might also like to see his PICC line, where all the chemo is administered. The docs and nurses are very pleased with the condition it is in, considering it has been in since January 8.

I took Josh to his first Bombers game at the G on Friday night. It was a fabulous game and Josh was in awe and completely focused on the game right till the final siren. Needless to say he fell asleep in the car on the way home!

** Update from Andi:

Tim has just been admitted back in hospital. Just now. Nausea too bad and he is dehydrated.

Friday, June 26, 2009

Update 26/06/09

Tim dictated this to me this morning....Andi xoxo

Hi everyone

I have been back in 6A since Monday. Just had my second round of 24 hour chemotherapy and unfortunately I have had a very serious allergic reaction to one of the drugs. After 15 mins or so into the infusion of Asparaginase,I came out with a massive rash, couldn't breath, vomiting, diahrea and a temp of 40+. My face is all puffy and my eyes are swollen. It scared the hell out of me, as I have not felt this sick so far. Luckily I do not have to have this drug again. I am slowly on the mend and I can't wait to come home. I am one step closer to beginning the re induction phase of the protocol, which will mean being an outpatient for the rest of my treatment ( approx. 100 more weeks ).

Thank you everyone for your support,

Love Tim.

Wednesday, June 17, 2009

Update 17/06/09

Hi all,

After a week in hospital and then a week home, Tim went back to 6A on
Monday for the repeat of the last chemo belt...... Unfortunately,
today he was sent home as his blood counts are too low to have the
chemo and it would be far too dangerous for him. A bit of a set back
and a major bummer as he had his own room this time. Tim will have
blood tests on Friday to see how his neutrophils and platelets are
going and if they are on the way up he will hopefully have the chemo
next week. (Funny to actually hope for chemo!!) Just got to roll
with it all.......

Tim's forehead is much better from the radiation burns. Just at a
peeling stage now, the redness has really settled. His headaches have
subsided for the moment, he is just extremely fatigued.

This week we had Christmas in June, thanks to our caring friends and
colleagues at Burke Hall. A fortnight or so worth of dinners plus
wine, teas and tea pot, soaps, vouchers, magazines, chocolates,
biscuit's, a cook book for chemo, a beautiful scarf for Tim, hand
cream and toys, books and puzzles for the children arrived on our
doorstep last Friday night. It was a the best surprise and Josh
refers to it as 'the day that was like Christmas'!!! Indeed it
was....we feel so loved and supported and are so very grateful to our
friends at Burke Hall who put so much thought into the incredible
hamper. It put a huge smile on all of our faces..........

Until next time.....

Lots of love

Andi

Thursday, June 4, 2009

Update 4/06/09

From Andi:

Hello everyone,

Tim was readmitted to ward 6A on Monday for another big dose of
chemotherapy. He had Methotrexate continuously for 24 hours followed
by Asparaginase the following day. The cranial radiation after
effects have come to the forefront with Tim having a terrible red,
burning rash on his forehead and shocking headaches. All this
compounded with the cocktail of chemo has left Tim feeling extremely
uncomfortable with pain in his legs, head and just the all over
'feeling like crap and I look like crap'. Poor Tim, he is very self
conscious of his forehead and his ability to gain 6 kilos in as many
days. He is still in hospital, unsure of when he will come home.
Thank God he has his ipod and dvd player to help pass the time and
block out the unfortunate wails and accidents of the neighboring
patients. It really is the most depressing place and it takes one
incredible mind and spirit to withstand the 25 or so nights notched up
so far. The hardest part is knowing that Tim has to go through it all
again in 10 days. AAAgghh.

A gigantic thank you to Andrew Hamilton for all his efforts in
organising the fundraising luncheon that was held in May. It was
tremendous to be able to bring Tim and say hello to everyone. It
looked and felt like it was a friendly and relaxed Sunday afternoon,
Tim and I certainly 'felt the love' when we walked in. It was a very
successful day and Tim, myself and the boys are so very grateful to
you all for helping us out at this unfortunate time in our lives.

Will be in touch with more news soon,

Loads of love

Andi

-------------------------------------------------

From the Admin:

Howdy! Finally got all the various issues with the Donate button sorted - if you are like me and couldn't make the lunch Andi mentioned but wanted to help out financially, you can use it to donate to an account for Tim and his family. It uses paypal, and may take a couple of days to leave your account once the donation has been made - if you have any questions of issues just email the blog.

Friday, May 15, 2009

Update 15/05/09

From Andi:

Hello everyone,

Tim has settled back home. It has taken a good week for him to build some strength back and is now sleeping and feeling better. Tim is preparing for radiotherapy to his brain which begins on Monday the 18th May and continues daily for two weeks. He had a great birthday on Tuesday and was so happy to receive the many messages from friends and family. He is now the man with STYLE after having received some fabulous designer attire....Polo Ralph Lauren, Lacoste, Tommy Hilfiger...certainly a long way from the bluey, yakka dacks and blunnys that was once his daily outfit! He looks so smooth......bald head and all!

We were lucky enough to meet Joshua's footy idol David Zaharakis last Sunday. For those of you who don't know, he is a rooky at the bombers this year and was the fabulous one who kicked the magnificent winning goal for the Bombers on Anzac Day!!! (...there..there....all you maggie supporters!) He signed Josh's jumper, footy and a couple of pictures. It was such a thrill for Josh and of course Tim ( and me too!).

Keep Smiling Everyone,

Love Andi

Monday, May 4, 2009

Update 04/05/09

From Andi:

Hello everyone,

Tim went back into hospital when the doctors predicted and has been battling his neutropenic state for the last 10 days. He has been running very high temperatures, had massive, violent shakes ( have forgotten the medical term for those) head aches and sweats. He has now lost all of his hair, most of his eyelashes and beard. He has been very sick and unfortunately I came down with gastro, so was unable to be with him for most of the last 10 days. He is compeletly 'over it' at present and just wants to come home. Hopefully this will be this week. His counts are back on the way up, so he just has to keep his temp down and then he should be home. This has definately been the hardest period (so far) for us all, as we did anticipate ........ but we are almost through it. Tim will have to have some more chemotherapy as an inpatient and we believe one infusion is for 24 hours! Nice. Looks like the next few months are jammed packed with chemo and radio. Surely cancer doesn't stand a chance with all this........

Bye for now,
Love Andi

Further Update:

7/5/09 - After just over 3 weeks away from us, Tim is finally home.
He is weak, thin, pale and completely hairless, but nonetheless home
and happy to be out of hospital. He is feeling a little down at
present but I'm sure some good home cooking and love and laughs from
family and friends will see him back to his normal self in no time. (
He hasn't cracked one bad gag yet....this is serious!) Next step
forward is radiation to his brain, which doctors are hoping will start
within 2 weeks.

Thursday, April 23, 2009

Update 23/04/09

From Andi:


Well everyone Tim has survived his power house of chemo...only
just....He currently feels like complete crap. He is out of hospital,
but only for a few days before being admitted again, where he will be
nursed through his neutropenic state. I suppose we wonder why he is
discharged at all, as he is completely bed bound....but home certainly
is better to be in than that horrendous ward 6A. If it wasn't for
Robbie, Tim's most recent stay would have been a living nightmare ( oh
...what...this isn't a dream....no, surely it is.....). It was so
nice for Tim to have someone young, positive, optimistic and who knows
exactly how he is feeling, right across from him to talk to. Tim and
Robbie should be in again together (both in neutropenic state) however
they will most likely be isolated. Unfortunately, Josh and I have
caught colds, so Tim has moved to his parents to steer clear of our
lurgy germs. The doctors have told Tim to come with a suitcase on
Friday when he has his blood tests, as they expect he will have to be
admitted. The boys and I miss Tim soooooo much.

The 'wall of courage' has again grown. The latest additions include
signed photographs with personal messages from, Kevin Rudd, Kate
Cebrano, John Williamson, Morgan Freeman, Peter Garratt, Pete and Myf,
'Straunie' and Eddie Mcguire. Tim also received a lovely 2 page ,
hand written letter from Tim Watson. Tim was so thrilled to receive
these, especially the letter from his childhood idol Tim Watson. Tim
was also able to ring him to thank him for his kind and encouraging
words . The letter and phone call all happened while he was in
hospital and really made his day.....he was absolutely blown away!

Unfortunately Tim was in hospital for Joshua's induction into the
world of AFL. Joshua just loved his first Auskick session and luckily
we filmed it all and took plenty of snaps. We definately have a
budding bomber on our hands. (much to Tim's delight......how much
better could it get? Both his son's love the Bombers, AC/DC and
fishing!!)

Bye for now

Love Andi




Wednesday, April 15, 2009

Update 15/04/09

From Andi:

Hope everyone had a great Easter break!! We all did!!!

Last week Tim had an update from Dr. Duggan, the head of Oncology at
the Austin. He is very pleased with Tim's progress as he is
responding very well to the treatment as he had hoped. His latest
bone marrow biopsy has come back 'all good' again which is fabulous.
The doctors have decided to delay Tim's radiation to the cranium for
another 4 weeks or so, as he was admitted today for his intensive
chemotherapy as an in patient. This entails chemotherapy every twelve
hours for 5 days, each infusion 3 hours in length. He is then
discharged until his neutropenic state hits, then he is hospitalised
again, given a strong course of antibiotics and nursed back to better
health. This is usually one week. He has been told that he will
become very ill, he will have fevers and temperatures etc...It is
unpleasant, but a necessary component of his treatment protocol.

Tim has been dreading this phase, as he now knows how it feels to have
chemo daily. This is more than double the dosage...so as you can
imagine he is anxious to see how his body will hold up. I have been
anxious but strangely excited for this phase. I have been thinking of
this as the rebirth of Tim. It will knock him for 6, but I know that
he will come through and hopefully that will be without any
microscopic nasty cells anywhere. Luckily for Tim, a friend he made
in Day Onc who is suffering Leukemia has been admitted in the bed
across from him. Rob has been through all this before and ironically
is a nurse at the Austin. He is a wealth of knowledge and one of the
few male patients in ward 6A under the age of 65. Between Rob, the
nurses ( who Tim is practically best friends with now !!!) his laptop
and newly found, very basic computer skills ( he can now google!!!)
the stay shouldn't be as monotonous as previously thought.

Love to you all,

Andi

--------------------------------------------------------

From the Admin:

Finally got our act together and have added a "Donate" button to the top left of the blog. This is linked to the bank account mentioned last post, and should hopefully make contributing to the Hamilton fund easier for those of us who spend way too much time online. If there are any problems encountered, email thehamiltonfamilyblog@gmail.com.

Cheers!

Saturday, April 4, 2009

Update 4/4/09

From Andi:

Hello everyone,

The Hamilton Family has had a great couple of weeks. This is all due
to Tim feeling so much better. The side effects from radiation
haven't been as debilitating as chemo, so Tim has been able to enjoy
some special family time, the most significant being Joshua's 5th
birthday. We had a small party for him with some kinder buddies,
where we had wild action zoo come to the home to give an 'Insect - a -
mania & mini beasts' show. Josh and Tim just loved it, as they share
a massive fascination of spiders, insects and bugs etc......(See
photos below) In the evening we celebrated with family, which was so
lovely to have everyone together. With a rest in between parties and
having radiation at the crack of dawn, Tim made it through the whole
day and we both had a smile on our face from start to end!

So, Tim has stood up to 3 weeks of radiotherapy to the chest extremely
well. Head aches and nausea have subsided and he is now just dealing
with a sore chest and throat and some heartburn and fatigue.
Apparently, the radiation continues to kill his cells up to 3 weeks
after the treatment ceases....so we will see how he goes. From
Tuesday 7th of April, Tim will be having a short break from treatment,
before recommencing with radiotherapy daily for 2 weeks to his brain.

We wish you all a great Easter break.

With love from,

Andi, Tim, Josh & Ben








From the Admin:

Apologies for the delay in posting this update - I've been away for the last week. If only I could teach Hammo to post these updates himself......

Things have been happening since last post. A bank account has been set up for those of us who would like to contribute financially to help the Hamiltons - the details are:

Enrico Peter Belli in Trust for Hamilton Charitable Fund
ANZ BSB 013-423, Account No 549041424

Once I'm a bit more organised (sometime this week) I'll set up a paypal link to this account and post it on the blog to make donations easier for everyone.

Cheers!

Monday, March 23, 2009

Update 23/03/09

From Andi:

Hi there everyone,

Tim has now completed week one of radiotherapy. The side effects are
just starting to take hold and these are heartburn and indigestion
(being new ones), nausea, head aches and fatigue. Even though the
treatment is fast and painless, it is uncomfortable and the side
effects do take their toll.

Tim has been unable to shake the severe headaches that have been
caused from the lumbar puncture last week. He now spends all day
lying flat on his back, as this is the only way he feels relief. He
tries to sit up for a few minutes each day, but really now he is
confined to bed, other than when he is driven to treatment and even
then we recline the seat right back.

We received very, very good results from the CT Scan that Tim had on
Thursday. The mass of tumors he had on his chest and lymphatic system
have completely shrunk in size and were not detected! This has
exceeded our expectations, as we were hoping for a reduction in size
and numbers. This is just tremendous news and given us all a real
boost. It is fabulous to know that the treatment, as harsh and
painful as it is for Tim, is working. His doctors have said that even
though his body appears to be disease free at present, the treatment
protocol must continue as planned. The 'blastic' part of his lymphoma
(which means baby cells that divide and multiply at an incredible
rate) is so aggressive, that the tumors can very easily come back and
bite him on the bum. That is also why treatment remains unchanged. He
will continue on the protocol as planned .....all 3 years of it. It
is still very early days, he is only 1/8 through his treatment, but I
say it is bloody good news and worth a little celebration! Fingers
crossed that all future scans and bone marrow biopsies bring this good
news.

TIM WOULD ALSO LIKE EVERYONE TO KNOW (ESPECIALLY THOMO) THAT HE HAS
JUST FINISHED READING A 450 PAGE BOOK IN UNDER TWO WEEKS!
Well Done Timothy!

Take care everyone and thanks for taking the time to read my updates.
Love Andi

__________________________________________

Admin note:

Progress has been made on setting up an account for those of us who would like to help out financially and we hope to post the details for everyone in the next update on the blog, if not before.

Also, a reminder about fundraising lunch being organised by Tim's brother, Andrew. If you have any items to donate for the auction, or any contacts or information you think might be helpful, please email thehamiltonfamilyblog@gmail.com and we'll pass the word on.

Cheers!

Monday, March 16, 2009

Update 16/03/09

From Andi:

Hi All,

This week has been a big reality check, after coming off a chemo free
week. Tim has had a full week of chemotherapy daily and also another
lumbar puncture, so he is back to feeling very sick, head achey and
exhausted. He has been bed ridden all week end.

Doctors have stressed to us this week the seriousness of Tim's illness
and his susceptibility to infections. It is extremely dangerous for
Tim to come into contact with anyone who is unwell during this phase
of his treatment. So we ask to be avoided please, if you or your kids
have anything of the sort......even a sniffle.

Thank you to Mick Stones and Dunc Thomas for keeping Tim company
during treatment this week. The nurses can't believe how up beat and
positive Tim still is ( it actually seems to worry them a bit). I
think they thought his 'personality' was a bit of an act and that he
would've piped down by now...they are still getting to know Tim. They
don't know what we already do, that Tim is a one of a kind and a
person who loves life and the opportunity to have a chat, no matter
what challenges lie in the way. Tim's favorite pass time would have
to be having a really good D & M with someone....anyone. That is just
who he is.

Another huge thank you to Daz McInnes ( a kinder parent who is a
builder ) for finishing Tim's screen fence at the back of the
property. It has been a work in progress for quite some time and Daz
came over last Friday and completed the job in a couple of hours. It
is great to see it finally finished and it also gives us a little more
privacy. It was very generous of Daz to give up his time and also
supply the materials. A top job! Thank you.

Poor Timmy. He has really felt so unwell this week......chemotherapy
taking its toll. Bloody cancer.

Love Andi.

Extra update:

Tim began radio therapy today (16/3/09). Chemo will cease during this
phase, except for the lumbar punctures. Today he had radiotherapy
targeted to his chest. This was the first of 16 doses to this area and
he will also have 10 to his brain. This all happens daily over 4
weeks. Tim said the procedure is painless, just very claustrophobic.

_____________________________________________

From the Admin:

Tim's brother, Andrew Hamilton, is in the process of organising a fundraising lunch for which invites will be sent out soon to everyone we have contact details for. If you're not sure whether you've already sent your details, please email thehamiltonfamilyblog@gmail.com to send them through.

Part of the lunch will be an auction for various sporting and entertainment memorabilia. If you have any items to donate, or any contacts or information you think might be helpful, please email thehamiltonfamilyblog@gmail.com and we'll pass the word on to Andrew.

Cheers!

Tuesday, March 10, 2009

Update 10/03/09

Hi everyone,

Tim wasn't able to have any chemotherapy last week, as his blood
counts were too low. Instead he had 4 transfusions, two on Monday and
two on Friday. His body is now ready for another slaughtering;
resuming chemo on Tuesday, another bone marrow biopsy on Wednesday and
a lumbar puncture at some stage.

It has been a lovely week, not having to rush to hospital everyday.
Tim has felt relatively good ( just headaches, mild nausea and
fatigue). I took him to the movies last Tuesday to see Grand Torino.
It was a great flick and fabulous to get Tim out, yet still be low key
and rested.

The highlight of our week was being VIP'S at Rove live on Sunday
night! (Anyone see us in the audience?) This was organised through
Rod, who had been in touch with Ben Lee over the last few weeks and we
were there as his guests! Tim rested all week end to have the energy
for this night and it was so fortuitous that he hadn't had chemo all
week, as he was feeling the best he had been for some time.

We were chauffeured to the ABC studio in Elsternwick (thanks to Rod
and Rach and Jannah and Mark) and seriously treated as VIP'S. We had
green room access where we met all the stars and shown incredible
hospitality. The champagne and sushi platters flowed before and after
the show and we just had the best night!!!! Tim had a fantastic chat
with Ben Lee, who is the most sincere and humble guy you could meet.
An absolute legend and Tim instantly connected with him. We had a
good chat to Rove, who gave me a massive hug on leaving and some
special words of encouragement.

It was such a special night and one we will never forget.

Hope you enjoy the snaps!

Love Andi

xoxoxoxoxo






















Monday, March 2, 2009

Update 02/03/09

Hi there everyone,

It has been an action packed week! Last Friday Tim was going to have
a hospital free day....unfortunately he woke at 5am with shocking bone
pain in his legs from the knee down. Straight to ED for a good dose
of morphine. Fourteen hours, two blood transfusions and many, many
hilarious, scatty, crazy conversations later (drug induced!), he came
home. So much for the hospital free day!

Tim had chemo every day this week plus another two blood transfusions
on Thursday. He also had another CT scan on his brain, just to
investgate the cause of some shocking headaches. Doctors were worried
that he may have had a bleed, but luckily it came back all clear. (
He does actually have a brain- just no problem with it!!!) Currently,
his red and white blood cells and platelets are very low and he is
borderline neutropenic. This means he is very susceptible to
temperatures and infection, so we have to keep a close eye on him this
week end. Any signs of the later, then he is back in to ED.

This week Tim has had lots of company during chemo. This has had a
big and very positive impact on Tim's spirits. Thanks to Macca, Luber,
Andrew H, Smiddy, Rohan and John H for making the hours of chemo much
more bearable. Thanks also to Mark Davies and our neighbour Tom, who
lent a hand tidying up Tim's precious garden at home. It was driving
him mad to watch it become over grown and out of control. You have
certainly restored some peace!

The 'wall of courage' is growing again! This week Tim has received
personal messages, signed dvd's and cd's and t-shirts from Daryl
Somers, Daryl Braithwaite, Roy & HG, Natalie Bassingthwaighte, Marcia
Hines, Roger Federer!!!!!, Jimmy Barnes, Metallica, a very special
message from Rolf Harris and Ben Lee!! and the absolute highlight: a
bombers footy jumper signed by Adam Ramanaskus, Dustin Fletcher, Jason
Winderlich, Mark McVeigh and Scott Lucas. Boy, does Tim feel special.
It is incredible to think how willing these celebrities are to go out
of their way to put a smile on Tim's face and indeed it does just
that!

Well, that is week 7 done..............only 131 weeks of treatment to
go!!!!!! (That doesn't sound so good, but for us it is going fast)
Tim said the other morning that this break from work is like the long
service leave he never got!!!! Yes, nothing quite like a well deserved
break at Club Austin!!!!! (and he wasn't on morphine when he said
that!)

Take care everyone.
Much love,
Andi
xooxooxoxoxxoxoxoxoxoxoxxoxoxo

Thursday, February 19, 2009

Update 19/02/09

From Andi:

Hi Guys and Gals,

Tim has had an excellent bone marrow biopsy result. All clear. No more
lympoblastic cells in his bone marrow! This was fabulous news for us
to receive, his body is responding to the chemotherapy.

He is back on track with daily chemo - everyday last week and 4 days
this week. This week he has also had a lumbar puncture, which is
chemo injected into his spine. He has felt nauseous and tired and
very light headed. Blood tests yesterday revealed he now has anaemia
and so today he had his first blood transfusion. This all seems part
and parcel of chemotherapy in high risk patients such as Tim. He is
handling this so well. He meditates in waiting rooms and is very
upbeat in hospital. The nurses just love him and he is Mr. Popular in
day oncology. (as I bet you can all imagine)

This week Tim was a case study for final year medical students. He had
no problem telling them his story from symptoms to diagnoses to
treatment. He was very open with them as they were also interested in
him as person rather than just medical guinea pig. Nice to know our
future doctors are so compassionate. We have found all the doctors
and nurses at the Austin to be this way. This also extends to the
extra care the hospital offers in the form of counseling and support
networks. Both Tim and I have received counseling and this is on
going throughout his treatment.

Tim is juicing like a man possessed. Everyday he goes through a bag
of carrots, oranges, apples etc. We have an awesome, new juicer
(thanks barb & john) and it has become a family ritual. We are keeping
our local organic fruit shop in business, almost every 2nd day I am
getting more supplies. ( I bet the bottle shop boys are missing
Tim.....he was on first name basis with all of them there!!) Tim has
said he wonders if he will ever have a beer again....at this point he
doesn't think he will.......actually both of us had our last alcoholic
beve on New Years Eve. I'm thinking if we hear good news in about a
years time we will be cracking some champagne for sure!!

Well, that's all I can think of for now.

Love to you all,

Andi

P.S. - Thanks to the following blokes, who pick up a blower and a mower for
THL this week:

Trent Collins, Chris Collins & Wayne Armstrong. We really do
appreciate that you guys give up you annual leave, retirement and
spare time. Thank you, thank you, thank you.

Tuesday, February 10, 2009

Update 10/02/09

Hi there everyone,

Hope you like Tim's "HOT" new look! Anyone want to follow his style
and for a great cause do the worlds greatest shave? Help the
Leukaemia Foundation raise funds for research and continue to provide
care and support for patients and families living with leukaemia's,
lymphoma's, myeloma and blood related disorders. It is on the 14th
and 15th of March, so go to www.worldsgreatestshave.com for details.

News on Tim..... He went back into hospital on Tuesday night after
experiencing chronic bone pain in his lower back. This was a side
effect from an injection he had on Sunday in his stomach to help boost
his white blood cells. A couple of days and a fair amount of morphine
later he came home..all good. This injection is a must have for his
condition and he is due to have a few more of them....so he may end up
back in hospital on these occasions. He has had a break from chemo
this week which has been fabulous and he has almost felt normal. On
friday he had a bone marrow biopsy. This test will let us know if the
production of the blastic cells are slowing down due to the treatment.
Lets all hope and pray that this will be the case.

The doctors have decided to delay Tim's radiation for another month.
So he will be having chemo 5 days this week, 4 days next week, 5 days
the week after and 4 days the next. At least he gets the week ends
off and every second week a long week end!!!!!!

More celebrities have sent tim well wishes! These include personal
messages and signed photos, books and dvd's from Natalie Imbruglia,
Casey Chambers, Laurie Lawrence, Chris Lilley ( Dicktation tag and
all!!!!), Kate Miller-Heidke, Tim Freedman of the Whitlams and a very
special card from Bert Newton. The 'Wall of Courage' is taking
over....we might need a pool room! Thanks again to Rod for organising
these for Tim. You should have seen his face.

Other thank you's must also go out to the following men who have given
up their time to work for Tim Hamilton Landscapes over the last couple
of weeks. All of them have braved 40 + degrees.
So a massive thank you to:
Luke Cheers - for giving up his Saturday
Matt Natoli - for giving up his Saturday
Chris Collins - for giving up his retirement!
Wayne Armstrong - for giving up every spare minute

and to Marcus Whitty for keeping Tim Hamilton Landscapes alive.

We appreciate all your efforts more than words can say. It means
everything to Tim to see his business continue trading and be in very
good hands.

We love you all so much.
Until the next update.......

Andi




Friday, February 6, 2009

Tim's new look


From Tim:

'My modeling agency has relinquished all contractual obligations and
finally allowed me to freelance my latest look....'