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Help Give Me Wings

  • Traveling with Paddy

      5 July 2022
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    When most people travel, it relatively easy to organise plane tickets, accomodation, pack suitcases and go.... To get ready for this trip, the word complicated doesn't even come close - it has definitely been an eye opener.

    Travelling with a disability ( and all the needed medical documentation) and an assistance dog definitely makes things interesting. I have been working closely with MPI New Zealand, USA and Canada in order to get all of the documentation, vaccines, blood tests, vet checks, accreditation certificates ( that Paddy is classified and certified as an International Assistance dog for medical purposes- Not an emotional support animal) Export and Import authorisation, quarantine when we return and a lot more. Oh and I can't forget- his own boarding pass and passport as he will be with me in the cabin vs the cargo hold.

    Today we spend the majority of the day talking with MPI Vets and export and import officials from MPI. At 5:30pm we received the necessary documentation, and went immediately across town to an MPI registered vet, so that Paddy could have tests for Rabies antibodies ( checking to see if the vaccine worked) and a general health check to make sure he was fit for travel. That all seems simple enough.. but wait there's more.

    This one blood tests has to be sent to Upper Hutt, which will then be sent to Australia for testing and the medical courier to Australia leaves first thing tomorrow morning. Major time constraint! luckily the vet, who lives in Upper Hutt, will take Paddy's bloods to the depot first thing in the morning so it can make it on the transport to Australia tomorrow. The kicker- this one test alone will cost around $1600 nzd and this doesn't include the other vet checks, vaccines, and medication needed for his travel.

    This is where donations like yours has helped so much.

    Aside from the vet issues, and MPI regulation paper work- which there is a lot!; A few other things have cropped up that I didn't know I had to do but have now done:

    I need a specific travel insurance policy that covers, all the normal things, but most importantly covers racing in a formal cycling event. Cycling NZ helped direct me to an insurance company that offers that policy. Which is then needed to apply for an international UCI racing license. Another thing which has now been completed.

    This has been such a learning process for me- its been complicated, extremely stressful and hard work. To be honest, there have been times that I have felt like giving up, But with every task completed, it moves us one step forward to our goal. I will not give up.

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  • 4 Weeks To Go - Getting Stronger

      24 June 2022
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    OK, just a quick update to let you know how the plan is going. Liz went to Auckland this week to get her passport renewed. As a USA citizen you have to actually physically go to Auckland and do the whole interview process. Hassle. Its a good example of how there's a ton of fiddly admin stuff to do making this come together. Liz had another round of chemo but her resilience and ability to train is getting better as she gets stronger and fitter. We did a race dress rehearsal with me testing her limits and Liz is producing record power levels now but will be even better in 4 weeks after the final build phase is complete. We did a cyclocross race as well and she had her best ever result. Flights, accomodation, race entries etc are all locked down. I told you Liz was the kind of horse you want to back. She is reliable, and hard working and her wings are looking good. Believe in her. I do. Steve

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  • Top Gun Maverick: THANK YOU!!!

      14 June 2022
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    Massive THANK YOU to everyone for making this an incredible night.

    I hope you enjoyed the movie!

    The weather definitely put on its own show for us. I hope you all made it home safely.

    Thank you all so much for coming, braving the wild weather and for your generous donations and support. It really means a lot.

    Congratulations again to all of our prize winners.

    Thank you so much to those who came out and braved the weather, and the companies who are so generous: Tailwind; Biomaxa; Fab Hair Co. Khandallah, Fitlab, and of course Petone Lighthouse Cinema.

    CAN'T WAIT TO SEE YOU ALL AGAIN SOON!

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  • Tailwind to the rescue

      10 June 2022
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    The only thing I have been managing to drink/eat since my treatment. I am very grateful for the fact that it tastes so good and its good for me.

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  • Ups and Downs

      10 June 2022
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    Over the last couple of weeks there has been some incredible weather, ranging from hail, thunder and lightening, beautiful still sunny days and icy cold gale force winds. Like the weather, things for me have been similar. Some awesome moments and some not so good ones... but that's life with MS or maybe life in general?

    Here is a brief overview as to why I've been a bit slack on the updates:

    About 3 weeks ago, when my family had covid- my body reacted to covid with a flare of MS which triggered some blindness. This was definitely scary. This lead to a few trips to the hospital for MRI scans, eye appointments and neurological assessments. I was put on strong antivirals which seem to have helped.

    Although my vision is much better now, I still have some issues which will likely to continue on and off.

    Once I was feeling mostly better- Steve and I celebrated by participating in the first race of the season in Cyclo-Cross. That was so much fun! With all the rain that we have had- it was definitely muddy- which makes it even more fun! This event was rounded out with a wonderful celebratory lunch at Brewtown (one of my favourites!)

    Then this last week was a bit of a hard one again I had another round of my Chemotherapy treatment for my MS. I usually do not feel that well afterwards and this time was no exception. But I have been very grateful to tailwind recovery

    ( chocolate flavour) to help keep up my calories and not let me get too Hangry.

    The most amazing thing that has been happening throughout all of this is seeing all of the amazingly kind and generous donations and supporting comments that have been coming through this page and through our fundraising pages. It's very humbling to receive these messages, especially during a time when I am struggling with my MS pain, sensory symptoms and lack of sleep. The treatment definitely doesn't help this in the short term but I have to keep thinking of the long term goals. Sometimes its hard to keep being positive... but after reading your comments it really helps. From the bottom of my heart, thank you. It really means a lot.

    We are now full swing into finalising tickets, accommodation and travel plans- its becoming extremely real!

    Onwards from here! What Fun! GIO!

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  • Hi Team, I’m Steve - Liz' Coach, reptile enthusiast and 1983 Under 7 Stokes Valley BMX Champ

      27 May 2022
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    Here’s a thing I learnt, and it applies to Liz.

    Suffering, sustaining training, and delayed gratification - that’s the core of what will make you a good bike racer - big lessons are never that sexy are they?

    If you want to know what these qualities look like, meet my Para Cyclist, Liz Gasson. She has Multiple Scleriosis, and her disease has made her suffer. Here’s a dirty secret I learnt from her. When you have disability, you don’t forget how it felt to have a healthy body - actually, you remember it all the time, and it sucks. If you have a degenerative disability like MS, and you want to succeed in cycling, then you’ll have to work harder and smarter than the next guy or girl and that’s just tough. Liz actually is that tough. She is the hardest, most resilient worker I know. She wants to get to the Paralympics, Paris 2024 and she will. I call her Water Bear but now I think about it she’s kind of like that creepy robot killer guy in Terminator. She will overcome every obstacle, and she won’t stop, and I believe in her.

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  • Our Wings are starting to flap!

      25 May 2022
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    Hi!

    Thank you all so much for your generous donations.

    Each donation received helps to add “feathers to our wings”.

    You might wonder why I use that analogy; walking is definitely harder for me than cycling. When I’m on the bike I feel like I’m flying.

    When I walk, I have difficulty with my right leg and foot due to the MS damaging the nerve pathways. I have something called foot drop and muscle weakness on my right side, plus numbness in my feet and my reflexes are not great either. I’ve been told affectionately that I sometimes look like a duck when I walk due to

    these issues.

    Unfortunately these symptoms cause me to trip, fall, loose balance or simply my leg collapse underneath me. I also can not feel my feet and I have nerve pain in my legs so walking hurts!

    But when I’m on the bike, I do not need to think about things like tripping or having my

    Leg give out. I wear a special brace that helps hold my foot in place and helps to reduce my leg pain.

    When I’m on my bike, I feel free!

    When I walk, I sometimes feel like I only have one working leg.

    That being said.. this is a good time to introduce you to one of our family members that you may not know about. She is still young, very beautiful and she’s very sassy.

    This is Violet, our one legged Pekin Duck. With her only having one leg, we are kind of similar. She hold a very special place in my heart.

    I have been thrilled to help rehabilitate waterfowl in connection with Wellington Bird Rehabilitation Trust.

    Violet is definitely awesome. She would definitely do well at the Paralympics for birds!

    Anyway that’s wee update from us.

    Thank you again for your help.

    It means a lot!

    Onwards and upwards from here.

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    • 26/05/2022 by Glynis

      Hi Violet - you're looking awesome. Hey Liz - we're so thrilled to watch and be a small part of your adventure. I also volunteer at Wellington Bird Rehabilitation Trust - what a great place, with the best team doing wonderful work...