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Sarah's fund

  • Update for 02/10/2014

      2 October 2014

    Enter details of your update here Hi all I have been updating my facebook page but suddenly realised there are a number of you who are not on facebook so are a bit behind in the saga of our lives! My apologies if this is old news.. Itfs less than 3 months until Christmas. Where has the year gone? I bought a 2015 diary today. This is a huge milestone as I was not expected to see the year out and now I am making plans well into 2015. I canft describe how good a feeling that is ? I know I wonft live forever as there is no cure for melanoma but these new drugs really are buying me time. Yesterday I had the third treatment of a new drug called Nivolumab which is one of the latest immunotherapy drugs for treating melanoma. The great thing is that I have this treatment in Tauranga every second week so no more trips to Wellington. It is so much easier to be able to drive 5 minutes after treatment and crawl into my own bed! The side effects of Nivo are so mild compared to chemo or Yervoy (which is the last drug I was on). Healthwise I am feeling pretty good. I still get tired quite easily and get very short of breath but otherwise I canft complain about too much. In face Mark and I recently had a week in the Cook Islands which we really enjoyed ? the girls were not impressed to be left behind but we just needed some time together alone and it was fantastic. We head off tomorrow for a week in Noosa (with the girls this time) and we are all looking forward to spending some time together as a family. Mark is as busy as ever and is almost finished his post-graduate Certificate in Development Studies (Ifm so proud of him), Hannah brought home an excellent school report last week and is doing really well with NCEA Level 1 (5th form) and Abigail was awarded most improved player in her soccer team and she also continues to do well at school. Both girls have lovely friends and the house sometimes feels like a railway station but we all love it. The pool is almost warm enough for swimming and a few warmer weeks will help. I am starting to think about work again and have a couple of leads for some project work. It will be healthy to start thinking about more than myself and spending hours researching my health condition ? I think I have become a bit boring and hope to avoid getting to the point where I need to be the centre of attention. So, if you need something done, you know where I am. Given that it is early days I will continue to fundraise in order to ensure that if this treatment fails I can get access to another trial drug. If I get to a point where I know this fantastic support is no longer required I will decide the best place to donate the remaining funds to. I will of course ensure that I let you know about this decision when the time comes. I hope this finds you all well as we rapidly approach the crazy time of year. Thanks for your continued support - without it I wouldn't be here today. Hugs, Sarah xx Sarah Speight 40 Fraser St Tauranga 3112 NEW ZEALAND 021 778580 sarahsp8@gmail.com

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  • Update for 02/10/2014

      2 October 2014

    Enter details of your update here Hi all I have been updating my facebook page but suddenly realised there are a number of you who are not on facebook so are a bit behind in the saga of our lives! My apologies if this is old news.. Itfs less than 3 months until Christmas. Where has the year gone? I bought a 2015 diary today. This is a huge milestone as I was not expected to see the year out and now I am making plans well into 2015. I canft describe how good a feeling that is ? I know I wonft live forever as there is no cure for melanoma but these new drugs really are buying me time. Yesterday I had the third treatment of a new drug called Nivolumab which is one of the latest immunotherapy drugs for treating melanoma. The great thing is that I have this treatment in Tauranga every second week so no more trips to Wellington. It is so much easier to be able to drive 5 minutes after treatment and crawl into my own bed! The side effects of Nivo are so mild compared to chemo or Yervoy (which is the last drug I was on). Healthwise I am feeling pretty good. I still get tired quite easily and get very short of breath but otherwise I canft complain about too much. In face Mark and I recently had a week in the Cook Islands which we really enjoyed ? the girls were not impressed to be left behind but we just needed some time together alone and it was fantastic. We head off tomorrow for a week in Noosa (with the girls this time) and we are all looking forward to spending some time together as a family. Mark is as busy as ever and is almost finished his post-graduate Certificate in Development Studies (Ifm so proud of him), Hannah brought home an excellent school report last week and is doing really well with NCEA Level 1 (5th form) and Abigail was awarded most improved player in her soccer team and she also continues to do well at school. Both girls have lovely friends and the house sometimes feels like a railway station but we all love it. The pool is almost warm enough for swimming and a few warmer weeks will help. I am starting to think about work again and have a couple of leads for some project work. It will be healthy to start thinking about more than myself and spending hours researching my health condition ? I think I have become a bit boring and hope to avoid getting to the point where I need to be the centre of attention. So, if you need something done, you know where I am. Given that it is early days I will continue to fundraise in order to ensure that if this treatment fails I can get access to another trial drug. If I get to a point where I know this fantastic support is no longer required I will decide the best place to donate the remaining funds to. I will of course ensure that I let you know about this decision when the time comes. I hope this finds you all well as we rapidly approach the crazy time of year. Thanks for your continued support - without it I wouldn't be here today. Hugs, Sarah xx Sarah Speight 40 Fraser St Tauranga 3112 NEW ZEALAND 021 778580 sarahsp8@gmail.com

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  • Update for 28/06/2014

      28 June 2014

    Hi everyone, I am sorry it has taken so long to post an update to you all. I got back from Wellington last night after another round of tests and appointments. A CT scan showed that since the last scan 6 weeks ago there has been no significant growth in my tumours and no new tumours. This is great news. I am feeling much better now that the side effects of the Yervoy are wearing off and am starting to get a bit bored which I guess is a good sign! Poor Mark! We are hoping that within the next few months I will get access to the new PD1 drugs which are showing such awesome results. In the interim we wait and assume the Yervoy will keep things at bay as it is doing for now. Thanks again to you all for your thoughts, prayers, donations, gifts, meals and other forms of support. As a family we are doing well - life goes on, doesn't it? - and your support is a huge strength for us. I hope this finds you all well. Much love, Sarah

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  • Update for April 2014

      1 May 2014

    Hi all and Happy Easter. We had the best holiday ever in Port Douglas over Easter and it was with great reluctance that Liz and I left everyone else there to return to Wellington for my final Yervoy treatment. It was 30 degrees, the snorkelling was amazing, the food awesome and we had a spa day to die for (oops...poor choice of expression!). The treatment today went well and now I just need to ride out the side effects for the next ten days or so. I am booked for a CT scan on the 14th of May and it will be interesting to see whether there has been some positive impact from the treatment. From then on I have a CT scan every 6 weeks and other monitoring every 3 weeks. The research team and cancer nurses enjoyed the chocolates I brought back for them. They are a great team and always make me feel at ease. Hoping you are all well. Thanks again for your continued support in the many ways you provide it. I will report in after the scan results come in. Our lovely friends Mark and Amy Wilson have orgainised a ""Mount Marathon"" on Saturday 3rd May where Mark and a few gutsy others will run up and down the Mount 10 times which is the equivalent of a marathon. If you would like to be involved or show support come on down to the mount on Saturday morning. Several donations for this have started coming into the page already. Thank you so much to all those involved and donating. Please accept our heartfelt thanks. Take care, S x

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  • Update for 03/04/2014

      3 April 2014

    Enter details of your update here Treatment number 3 today! Can't believe how quickly 3weeks comes around and I'm back in Wellington getting jabbed and loaded up with this tumour destroyer again! The two weeks after the last treatment were pretty bloody awful and I am told to expect that again. While I am not looking forward to this, as long as it is doing its job I'm okay with it! As a family we are overwhelmed by the generosity of you all and send a heartfelt thank you for your donations, letters, emails, prayers, meals and visits. Sarah Xx

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  • Update for 10/03/2014

      10 March 2014

    I head down to Wellington on Thursday for the second treatment. I'm partly excited and partly nervous. The side effects from the first treatment laid me low for 10 days but I'm hoping this one will be a bit less debilitating. Mark is coming with me which is great support and it will be great for him to be able to meet my treatment team who are all lovely. I will let you know how it goes! S x

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