Back to page

Kelleigh Burkett

  • UPDATE FROM KELLEIGH 21/04/14

      28 April 2014

    UPDATE FROM KELLEIGH: This might seem long but lots to say lol hope you are having a fab Easter. We are resting and enjoying home time. xxxxx Well this has been the most difficult, challenging and frustrating 8 weeks for our family. I have had 2 treatments fail within that time, radiation on my Brain that has left me with terrible short term memory loss and I am being weaned off the steroids due to brain swelling but this is leaving me fatigued, head-achy and unable to sleep all night. I am thankful that I'm still here but one of the hardest things I am dealing with is loosing my independence, not being able to drive and the fatigue. My family is my world and I will do anything to protect my girls. Its been a challenge to give age appropriate information to them. We live day by day just like the kids do and try not to think about the future. We create memories everyday, laugh, love and enjoy the small things like the rain on my face and the wind in my hair, which is starting to grow believe it or not. As you are all aware, Craig and I flew to Sydney for our appointment with Dr Friedlader who was a very kind, caring and gentle soul and we are greatful that he could see us. We had some good and not so good news. I am unable to get on the PARP inhibitor trial due to the current Chemo drug that I am taking. It basically excludes me from the clinical trial completely. But, the good news is that there are drugs in Australia that we can pay for that are not available in New Zealand. There is a drug that can help make Hormone treatment more effective which will cost $50,000 for a year, plus I will need to fly to Sydney every month to have it. As a family we don't take this lightly, the outcome will be the same but this may just give me more time with my girls and i do believe I could be the one of the 5% of people that defy the odds. There are also other Chemo options that we can look at down the track but unsure of the cost of these at this stage as we are still waiting for the report to come through. I am due for a CT scan in May and this will determine the next line of treatment. I am hoping that the current Chemo pills I'm on are holding things stable, but am fully aware it may not be working. As the Professor said, there is no cure but we have some options to give you more time if they work. I will be attending the Ian Gawler retreat in Auckland in mid May for a week which I'm really looking forward to, it's for people living with terminal cancer. The below is an overview of the course copied from the program. ""This program will provide a gentle blend of theory and experience. A wide range of choices will be presented for you and their relative merits for healing and wellbeing discussed. The emphasis will be on what has been found to work in practice, what the research says, and you will be assisted to decide what is best for your particular situation. The program is evidence based and highly experiential, so you will have the opportunity to learn as well as to experience the food, practice the meditation and to be in a supportive, positive atmosphere. The aim is that you will go home from the program having experienced the possibilities and that you will be clear about your choices, confident regarding what will help you most directly, and ready to apply it all in daily life. What we are talking of is not gAlternative Medicineh, nor even gComplementary Medicineh as such, although all of this is designed to complement any other treatments you may be having. No, this is Lifestyle Medicine and it is to do with the therapeutic impacts of what we eat and drink, our levels of exercise, our relationships, the state of our mind and our capacity to mobilise the power of our mind using techniques such as positive thinking, relaxation, mindfulness, creative imagery and meditation. You will learn more about the role Lifestyle Medicine plays in overcoming the many challenges of cancer; including the science relating to the therapeutic benefits of nutrition, positive states of mind, mindfulness and meditation. There will be good time for questions and discussion. Regular relaxation, mindfulness, meditation and guided imagery practice sessions will be a feature. The pace of the program has been designed to be restful and regenerative, amidst a valuable learning experience."" From Ian Gawler. The incredible fundraising events that have been held and are going to be held have blown us away. It was really hard to get our heads around accepting money, but we are so grateful - from the bottom of our hearts - for everything. We Are all so grateful for the photo sessions, rides, lawn mowing, gardening, help from friends, and delivered meals that keep things going. I couldnft do it without the friends that have the kids for play dates, take me to doctorsf appointments and those who offer assorted favours. I need you more than you know and am grateful to those who offer. Life is short, break the rules. Forgive quickly, kiss slowly. Love truly. Laugh uncontrollably and never regret anything that makes you smile. Mark Twain Love Kelleigh x

      0 comments  |  Login to leave a comment
  • UPDATE FROM KELLEIGH 31/3/2014

      31 March 2014

    Well it's been a long tough week, harder than I thought it would be. The Whole Brain Radiation symptoms kicked in when we got back from our weekend away, I was so glad to have such a relaxing weekend. Earlier in the week I had been struggling with nausea, headaches and dizziness, (maybe a good thing I'm not allowed to drive!) but I've managed to get on top of it by adjusting my medication. My Dad sprung a surprise visit on me last week to help out with the kids and get me organized. He has been helping me with everything medical and drove me around like I had my own personal assistant. Time spent with my Dad is always full of laughter, as well as we managed to squeeze in a lovely breakfast out. Monday 31st March 8am: I am flying to Dunedin with my Mum, to support me, which is fantastic! But this also means leaving my girls at home with Craig. Craig will be working reduced hours for 3 days to do all of the pre and after school care. WHAT A GREAT HUBBY AND DAD YOU ARE!!! So thank you to everyone in advance for the meals and baking which is being dropped off each week. It is much appreciated, tasty and one extra thing we donft have to worry about. Today (Monday) I am having a MRI scan and CT scan to map out the tumor on my brain and have more blood tests. On Tuesday they make my head mask/mouth guard thingy to keep me immobilized for my Stereotactic Radiation Therapy. Check out an explanation of this treatment here: www.rtanswers.org/treatmentinformation/treatmenttypes/stereotacticradiation/#. This treatment is scheduled for 6pm Tuesday evening, then, I have a follow up appointment on Wednesday morning and back home by 5pm Wednesday. We are operating on very tight time frames. I'm feeling anxious and nervous but this is the next step in getting me healthy and being able to be here with Craig and the girls. At the same time as everything else I am having oral Chemo 10 days on and then 1 week off. Our first appointment in Sydney with Dr Friedlander is booked with us ready to fly out on the 13th April for 3 nights. I will post an update on this closer to the time and more details. We have also ordered the first of CTC tests from Australia which was AU$4550. This test would not have been possible for me without the money that has been donated from everyone! The Comprehensive CTC Test is for people with a previous/current diagnosis of cancer. This test includes the isolation and identification of CTCs, Gene-Expression Profiling, and analyses a personfs individual cancer cellfs response to chemotherapy agents, monoclonal antibodies, hormones, botanicals and nutrients. (This is the Genostics test). Please click here for more information on the CTC Test: https://www.genostics.com.au/general/test_list/ We are also having a huge box of organic vegetables and fruit delivered each week to fit in with my special dietary requirements and this is also made possible from the donated money. I will let you all know more once I am back! Kelleigh x

      0 comments  |  Login to leave a comment
  • UPDATE FROM KELLEIGH 15/03/2014

      15 March 2014

    UPDATE FROM KELLEIGH: Well so much is going on its hard to keep up myself! This is the latest: Looks like I'm heading to Dunedin on the 30th March for the next step of my radiation treatment for the brain tumor which is great news. Then on the 13th April Craig and I are flying to Sydney to see Prof Michael Friedlander to try and get onto a trial drug called a PARP inhibitor. This is not available in New Zealand but is showing some promise. The PARP inhibitor is designed to repair the PARP (PARP, which stands for ""poly (ADP-ribose) polymerase,"" is a family of enzymes found throughout the body. PARP is needed for a form of DNA repair known as break excision repair, which fixes glitches in one strand of DNA.) A fantastic explanation of PARP and the PARP inhibitors is found here: http://www.dana-farber.org/Newsroom/Publications/PARP-inhibitors-on-trial.aspx Please read this article as it will help you better understand why we are pursuing this avenue of treatment. I carry the BRCA2 gene, only 5% of all breast cancer suffers carry this gene so you could say I am very special. My 3 daughters have 50/50 chance of inheriting this gene from me and puts them at risk of Breast/ovarian cancer as early as in there 20's but I'm sure they should have a cure by then. We will be funding this trip to Australia out of the money which has been donated, so to us this is fantastic. If I get approved for this trial drug it will be administered at St Georges Cancer Care clinic here in Christchurch, which is a private hospital. New Zealand has less available options than Australia so we are giving everything a go. Just on a side note we found out yesterday that Craigfs work has been reduced down to 4 days a week. Though this means we will have more wonderful time together this will also put added pressure on the budget. But, we are good at managing this side of things. Thanks again for everyone's support All my love Kelleigh

      0 comments  |  Login to leave a comment
  • UPDATE FROM KELLEIGH 12/3/14

      12 March 2014

    I have had two days of hospital appointments to sort out a plan of attack to get my brain tumor under control. To do this I will be starting whole Brain Radiation (WBR) on Thursday afternoon. This is 5 days of radiation of my whole brain each day, very scary! Side effects will involve complete hair loss but new funky wig! Also nausea, vomiting and maybe some other slightly unappealing things. After this I will be sent to Dunedin for Stereotactic Radiosurgery (SRS) which is a minimally invasive form of surgical intervention without the blood and anesthetic. The only problem remaining will be my liver, which has a lot of cancer activity that we canft control (this is the life threatening part so I will be trying a new chemo drug as the last one has failed me). I am also looking into overseas treatment options. All this is to buy me some time as there is no cure but I intend on living and loving the best I can. I am humbled by the love and support of everyone and will not let the cancer win..... My life is filled with love and everyone in it who makes my life whole. Thank you again for everything xxxx

      0 comments  |  Login to leave a comment