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Happy New Year everyone! Our family had a very nice holiday season with all of my progress, and Santa (& family & friends) spoiling us all rotten. Hope your families had a wonderful holiday season as well.
I did want to share a few highlights of my Christmas with you...I've been receiving gifts since I've arrived in hospital, but Mickey brought in an autographed photo of Roberto Luongo...which is now framed and waiting to be hung. Then Kirsty got a parcel in the mail from R. Orr in Florida, which was Bobby Orr's famous 'leap of faith' photo with a personal note signed by Bobby Orr which Kirsty had framed for me for Christmas. I want to hang it in the dining room, but Kirsty's not sure about that
I don't know how he found out...but thank you whoever told him! On Christmas day, Deanna, Scott and their boys came down with Cheryl's delicious Christmas dinner for me, and suprised me with an autographed Roberto Luongo jersey, a Canuck hat signed by Ryan Kessler, and a Trevor Linden retiree pennant - Deanna's not a hockey fan, but boy does she have connections! Tanner, Kobe & Rhys also gave me a Superman t-shirt, because I've told them (and they know) that I am Superman and am going to overcome this injury.
I cannot thank everyone enough for all the gifts, but these ones are definitely the envy of the ICU (well, maybe not for those TO & Habs fans!).
I have been progressing well. I have been breathing off the ventilator and have been going for 16 hours/day for the past five days. When I'm off the ventilator, I have a valve in my traecheotomy that allows me to speak. It's far less frustrating and much nicer for me and the people around me. Kirsty says it's great to hear my voice - never thought she'd say that ![]()
Lexi, my physio-terrorist has also been putting me through the ringer. I have gained some motion in my right arm allowing me to move it slightly, so Lexi has rigged up a some resistance bands to remove gravity from the picture, which allows me to exercise this more freely.
Nicole, Jen and Sandi (my three primary caregivers) have also been pushing me. Nicole ripped my feeding tube out on Christmas morning, so now I get to eat my three squares a day, plus snacks. I've lost some weight so they're trying to fatten me up a little
Jen was checking my range of motion and noticed when I was trying to wiggle my toes on my left foot (which I'm very good at), that I can now flex my left foot at the ankle as well. These three sound tough, but they truly are angels and there is no doubt in my (or my family's) mind(s) that I wouldn't have progressed this well without them and Lexi! Thank you ladies!
2009 is looking to be a good year. Kirsty has been checking out rehabilitation facilities and we are looking at Ottawa or possibly Toronto, or even possibly Kingston if I get off this ventilator. My family and I know it's a very long road ahead, but we want to thank you for your continued support - it's been absolutely incredible!!!
Scott, Kirsty, Tanner, Kobe & Rhys (aka Team Milne)

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