I guess most of us girls would but it was wonderful for “Wainwright’s Coast2Coast MS Walk” to be acknowledged at MS Research Australia’s 2014 Kiss Goodbye to MS launch at NSW Parliament house last night as 2014’s FUNDRAISING EVENT OF THE YEAR. And we haven’t even started. The pressure is on girls but you are over well over 25% of the way and with further fundraising events to come and donation support from family and friends we will achieve our goal of raising $150,000 for research into a cure for MS.
My wonderful husband spoke from the heart about the struggles he faces each day and how the disease’s progression has forced him to constantly readjust how he does things. Resting before attending these events is now mandatory if he is to give himself the best chance of delivering his speech in the way he would like. An accomplished public speaker Mike now relies heavily on his notes to ensure he doesn’t forget what he wants to say. I, on the other hand, know exactly what I want to say but rely heavily on my notes to ensure I deliver my message with the confidence and ease Mike has never had to grapple with. We are an excellent team and I so much admire him for the support he gives me to continue telling our story and for his tenacity to keep on going despite MS’s constant presence.
Here’s Tansey Keys giving Mike a few tips on how she plans to get over those fells.
It was a thrill to have 12 of the 17 Australians walking all-the-way attend the event last night. With 5 more to be added I think we could do with a photo shoot organiser. Just squeezing 11 (sans Liz McDonald who was somewhere in the room) and Mike into this photo proved quite a challenge. Happy for advice on how we best position 20 people (including 3 Brits also walking with us) for the many photo opportunities that will invariably arise with majestic Lake District, Yorkshire Dales and North York Moor backdrops, and then the pub shots as well as we toast the end of yet another successful walking day.
As I mentioned in my speech two of the girls walking with us have MS. The disease is often called the invisible disease because you can’t spot the varying symptoms people with MS may be experiencing at any one time. Can you see numbness, nausea, dizziness or altered sensation such as pins and needles or even partial blindness and cognitive impairment? If you didn’t know them I suspect it would be difficult for you to spot the girls in this photo living with MS.
But I suspect you can see these lovely ladies, Denise and Sally having their way with my husband. Hey girls! Hands off. He’s taken.
After we left the event Liz and I didn’t make it past the beautiful vestibule of this historic building without ripping off our shoes. Too used to wearing appropriate footwear we found the evening a huge challenge for feet not used to high heels and being squeezed into pointy toes. Oh, for a hiking boot. With a band aid on most toes we’ll back out at this weekend walking from Cowan to Brooklyn as we prepare for this fantastic event.
Please continue to support our event by clicking this link to donate. Or come to Eastern Rd Quality Meats Turramurra this Saturday May 3 from 8.30am and enjoy a sausage sizzle with Denise Temisgian and Katrina Hemingway serving you. Our thanks to business owner, Allan Waldon, for hosting and donating all the goods to assist us maximise our fundraising dollars.







































