Back to page

Leanne Thompson Fundraiser

  • Thank you everyone!

      8 June 2016

    I am overwhelmed by the amount that everyone has raised! I cannot express how much this means to me and everyone's generosity just blows me away!

    On a medical note, I got into remission on my first round of Blinatumomab, and am now currently on my second one.

    The next step is getting a hospital in New Zealand to give me a second transplant. Historically, it is not a normal thing here in NZ. The Australian hospital is happy to do it, but cost wise I'd like to do it at home.

    For my third round of the Blin they/me would love to do it at home, here in NZ. That is all in the pipeline, so fingers crossed.

    I am so happy that I am healthy, and still smiling.

    Life is precious!

    Thanks to everyone!

    Leanne xox

      0 comments  |  Login to leave a comment
  • First week of Blin-cyto done!

      19 April 2016

    I have just finished the first seven days of the Blin-cyto drug here in Melbourne.

    Tomorrow, I'll be going up to the full strength of the drug, and I'll be closely monitored for reactions for a few days before becoming an outpatient, whilst still carrying around the pump with me.

    Already, there are some indications that the drug is working - basically, two proteins are joining forces and creating an army ready to attack the leukaemia cells.

    We are amazed at the effort of Room 14 and community, and blown away by the money they have raised from the 'Fun to Givealittle' day.

    Thank you so much!

      0 comments  |  Login to leave a comment
  • Melbourne here we come!

      3 April 2016

    I got the call that I am wanted in Melbourne to begin my Blincyto journey as early as the 11th April! The drug company is providing the drug on compassionate grounds. It is no longer a 'trial' - that finished in Nov 2015. I am going to be 'No.3' on the compassionate list!

    So what's next?

    First I have to pay the hospital upfront for all the surrounding costs.

    Once I get there, I have a couple of outpatient days to do some checks and put a line in, then I'd start treatment as an inpatient.

    As far as I'm aware, treatment involves being hooked up to an infusion pack, firstly in hospital for 2-3 weeks (increasing dose, dealing with potential side-effects), and then 28 days out with the pack, coming into outpatients twice a week for checks/change of pack. Two weeks off, then begin the same cycle again. The drug company has allowed for four rounds, however the Dr seems to think two will be enough. The decision of 'what happens after?' will be made then - bone marrow transplant, or get on with living!

    A lot of stuff has happened between being diagnosed on the 1st March and being told I'm accepted to Melbourne on the 1st April... 4 rounds of chemo, countless blood tests, meetings, and crossing of fingers and toes! All is headed in what I hope is the right direction for me!

    If I have to fly out this weekend, I will miss the wonderful, amazing, generous fundraiser the school is doing, but they will know I am thinking of them as I wing my way to a better outcome!

    For those that would like to follow my journey, I have a blog that I update (and will try to do often!):

    cancerandmetimes3.blogspot.co.nz

    What is it I'm actually having?

    The Technical Answer...

    Blincyto ® is classified as a monoclonal antibody. Monoclonal antibodies are a type of "targeted" cancer therapy.

    Antibodies are an integral part of the body's immune system. Normally, the body creates antibodies in response to an antigen (such as a protein in a germ) that has entered the body. The antibodies attach to the antigen in order to mark it for destruction by the immune system.

    To make anti-cancer monoclonal antibodies in the laboratory, scientists analyze specific antigens on the surface of cancer cells (the targets). Then, using animal and human proteins, they create a specific antibody that will attach to the target antigen on the cancer cells. When given to the patient, these monoclonal antibodies will attach to matching antigens like a key fits a lock.

    Since monoclonal antibodies target only specific cells, they may cause less toxicity to healthy cells. Monoclonal antibody therapy is usually given only for cancers in which antigens (and the respective antibodies) have been identified already.

    Blincyto ® is a type of monoclonal antibody called a “bispecific T-cell engager” (BiTE) antibody. It works by directing the body’s T-cells (part of the immune system) to target and bind with the CD19 protein on the surface of B-cell leukemia or lymphoma cells.

    (Taken from http://chemocare.com/chemotherapy/drug-info/blincyto.aspx)

    Leanne Thompson :-)

      0 comments  |  Login to leave a comment
  • Update from Leanne - Medically what's going on!

      21 March 2016

    Update as of 21 March 2016

    First off, I have to say that Gavin and I are absolutely blown away, extremely humbled and grateful for the love, support, donations from friends, colleagues, family, and strangers. We are incredibly lucky to have a community around us as we go through this once again!

    Medically speaking, I am currently on a weekly chemo dose to try and knock my leukaemia back into some form/close to remission, in order to see what to do next. This week I will be having a check on my spinal fluid for any leukaemia cells (so far, this has been clear), and next week I will have another bone marrow biopsy to check progress of remission. I am still feeling pretty well, apart from some tingling on my tongue and fingertips (from the chemo).

    I am awaiting approval for a trial drug called Blin-cyto, which is a antibody, not a chemo. It is an immunotherapy, where it stimulates your t-cells (infection fighting cells) into action against the leukaemia. This was developed in Germany, however, they are not currently doing it there at present. The Dr who developed it told my Dr that they are using it in Melbourne, with varying success. It is quite a new drug, so no hard statistics, but they can do it with me not being in remission (it would work better if I was though). After 2-3 months treatment/infusions in Melbourne, I would come home and possibly have another bone marrow transplant - or not (there are cases either way for long term survival - just don’t ask me what that is yet - as there is not enough info). Auckland has said they are unlikely to do that again, leaving my team to look at other centres around NZ if that opportunity presents itself.

    We have asked the Dr in Melbourne to go ahead and seek approval - this will take at least 3 weeks before we know if I will be eligible for it. The cost of the drug, if approved will be covered (as far as I am aware), however, the surrounding costs of the specialty hospital, nurses, outpatients, tests etc, etc are a minimum of $100,000 AUD.

    I know I am extremely fortunate to still be alive after fighting this on and off (plus some breast cancer in-between) since 2007, and I am going to take every opportunity to keep living and fighting. Giving up has never been an option. When my Haematologist (who has had me since 2007) looked at me with an upset look in her eyes, and said ‘It’s back and we’re quite limited in what we can do’, my response was ‘Well, whatever you can do - you need to do it. I have no time for this, I am far too busy living to stop and cause chaos!’

    A wise man (you know who you are) told me - 'Leanne, you can’t kill weeds’ - and he is right - I will be like a gorse bush, covered in blackberry that you just can’t seem to ever get rid of ;-)

    Big update for everyone - and I will update this page more as I know more myself. I am once again truly grateful for everyone’s support.

    Thank you to the fabulous teachers and awesome Room 14 for organising a fundraiser for me too. I will be there!

      0 comments  |  Login to leave a comment
  • Room 14 Fundraising Day

      18 March 2016

    Leanne's class are holding a fundraising day on Sat 9th April at Omokoroa No 1 School. Come along from noon to get your car washed, have one (or more) of Mr Joe's famous dumplings, go on a pony ride, buy some bargains at the mini-market, car boot sale and Virgin Jewels stand. For entertainment you can watch Lulu Johnson raise funds with a swimathon or watch our lovely teachers, Mrs Little and Mrs Ryan shave their heads to raise funds.

      1 comment  |  Login to leave a comment
    • 18/03/2016 by Omokoroa No1 School Staff & Community

      Yes I'll be bringing lots of friends and family!!