Wednesday, December 15, 2010
Friday, December 3, 2010
Hi all, Erin here
Its day 2 now since he had the peg inserted and he's been in bed since we got home from the hospital, not sick just feeling abit bruised and battered. I'll get him up tomorrow and we can potter around outside in the garden or something.
We are in the process of transitioning from the standing hoist to the sling hoist. That was a big call. But its starting to get more difficult for us using the standing hoist. His back isn't as strong as it was and you can feel he is just a wee bit "floppy". His legs can hardly bare any weight at all now. Having said that, on a good day we will use it if I have someone else that can support him from behind while I operate the hoist. The sling hoist will be alot easier for him and me they say.We've got a week or so with the two hoists and then it'll be byebye to the standing hoist forever.
Other then that he has been doing absolutely fantastic. Still eating like a horse and yes sometimes he eats what he isn't supposed to. Been out and about going for drives and things and that's been great.
Just want to send you all our best wishes for the festive season now, because knowing me I won't be on here again for a while, not enough hours in the day just at the moment. Cherish your loved ones, honor the memories of those who have passed on and honor yourselves enough to know that you're the best person you can be.
Meri Kirihimete - Merry Xmas to you all wherever you are.
The Gardiners
Saturday, October 9, 2010
Erin Here!
Hey, just a quick note to let you all know Bill is well. We still haven’t been anywhere on the van. Had some really awesome weather the last couple of days, but while the kids were on school holidays, we took advantage of the time to get out and around the house, lawns, gardens and all those mundane things that have been sorely neglected just lately. Then the rain came back, so Bill decided to stay in bed.…….but he’s feeling good because he was able to potter around in the garage a little bit. Amazing how you take those little things for granted. He can’t hold a yard broom or a rake anymore, but did a fine job of supervising, and for once got no arguments from the kids. All things considered, he’s doing really well and remains as positive as ever.
If you haven’t checked out the new-look MND site lately go check it out, they now have an interactive forum for caregivers/people with MND etc etc. Its looking pretty good follow the link on the right hand side of my page and go have a nosey. I’ve made a new friend in the forum already with one of its members who lives in Thames, he is the main caregiver for his wife and we spent a bit of time this afternoon talking about Bill and Jude (his wife) and generally just comparing notes. Anyway, I look forward to keeping in contact with him now and hopefully will get to know a few more people as time goes by. While its awesome to have friends and family to help out there is nothing like talking to people who are walking in the same shoes, being able to help each other out if required or just offering a knowing shoulder of support.
Speaking of friends, have been in regular contact with Joan in Canada since her darling Rick passed away. She’s finding it really rough going as I’m sure we all would coping with the reality of life after the loss of a loved one. She’s a pillar of strength Joan is and while she struggles daily at the moment, some day when she’s ready she will be able to embrace what ever lies ahead for her.
That’s about it for now, will check in again soon.
Erin
Tuesday, September 21, 2010
Have van, too dang cold and wet to go anywhere…..
Hey, Bill here.
Celebrated my birthday on the 7th of this month and got a special present delivered to my door……Yuss, got my van! Only one problem, I haven’t dang well been anywhere on it because the weather has been absolute crap……TYPICAL! Actually that’s not strictly true, my birthday fell on a Tuesday, and it cleared up the following Friday afternoon for a couple of hours. So, Erin got home from work, got me up out of bed, put some warm clothes on me and said “its now or never mate” lets go!
She locked and loaded me, LOL onto the van, and we took off around to our sons flat, rang the doorbell and surprised him with Me (and the van of course), It was still really cold so I didn’t get out of the van, just sitting in it enjoying being away from the house in comfort. We were there for a half our or so and then we drove around to the ocean beach while it was still light, we parked up and just sat there enjoying watching the surf. Didn’t say much just sat there until it got dark and then we came home. I really enjoyed that drive, only one downside to that trip, Erin forgot her purse, and I wanted an ice-cream, got the huffs because I couldn’t have one….hehehehe, nah just joking, was just happy to be somewhere other than home for a change.
Since then we’ve had nothing but rain that was 2 weeks ago, hopefully the weather will change for the better sometime soon, but the forecast isn’t looking too promising for this week anyway. Still at least I know when the weather clears I’m outta here, don’t know where I’m going but believe me I will be going…..LOL.
As far as my general health is concerned I’m feeling pretty good really, just the cold gets me. Fingers crossed things will remain this way for a while. Erin and kids are all well, had my mum down last weekend for her sisters 80th birthday. Its always good to see her, especially when she brings me presents and food, hehehehe.
That’s about it folks, same ol dull routine for the most part, but with a bit of luck that will change shortly.
Laterz, Bill
Oh, before I go, I promise to take some photos when I do manage to get out, and post them on here.
Saturday, September 18, 2010
Erin Here!
Several weeks ago, we lost our friend Rick in Canada who we have talked about quite often in our previous blogs. He left our world as he lived, humbly and graciously. When we started this blog it was mainly to keep Bills family and friends informed about Bill. There are any number of stories both funny and not so funny that we could share but Bill has always been a very private person and we only ever post what he is comfortable posting. So for the most part we tell some of the story and not all of it.
Rick and Joan on the other hand without fail always told “the whole story” warts and all. I would think to myself as I read their blog, holy heck all the while admiring their courage. When Rick passed away I actually contemplated not telling Bill straight away because I wasn’t certain how he would react. (For the record though, I did tell him straight away). Having never met Rick I couldn’t say with any certainty but reading his blog I really think he and Bill shared the same quirky sense of humour. They for sure shared a shit of a disease but they both also shared a really really positive outlook for themselves.
Rick! Soar free with the Angels our friend.
No more are you confined by disease in a motionless shell
You’ve been released from your earthbound hell
Soar free with the Angels our friend
Watch over Joan as she watched over you
For her, a new journey ensues
Bless her with love and strength to mend
Soar free with the Angels our friend.
In memory of Rick, a hell of a guy.
Dedicated to Joan a hell of a gal.
Wednesday, July 28, 2010
Tougher by the day:
Every day at the moment brings a change in Bill’s condition'. Since leaving the hospital over a month ago now, Bill has spent the vast majority of his time in bed on his bi-pap. He remains forever positive but he struggles now to maintain what little independence he still has. He still has excellent swallowing, eating and chewing so that’s definitely a positive. On the downside he is very weak and gets very tired very quickly. We have a new care plan in place with increased hours for our caregiver. She is here 5 hours a day, 3 days a week at the moment. We’ve managed to work her hours around my work and the boys polytech hours, so that there is someone with Bill 24/7. Luckily for us our caregiver happens to be one of my closest friends, so if the kids aren’t pulling their weight, “aunty Di” will “deal to them” for me. And if I’m not pulling my weight well she’ll tell me off too. We’re also able to be more flexible about whose around and when, because my job allows me to work my hours around what’s happening at home. We’re hoping that for the time being at least things have reached a plateau for Bill but we have come to realise that in the blink of an eye, this disease can take a turn for the worse. Just want to make special mention of our “team” of dedicated professionals, Fiona and Anna-Marie (speech therapists), Krystal (our OT), Sue (Physio), Rose and the palliative care nurses from the hospice, Bills awesome GP, Stuart Lydiard and last but not least our family and friends who appear out of nowhere just when we need them.
We are still searching for a mobility van, one did become available but did not have enough passenger seats in it for all of our kids as well. They wanted us to take it, but Bill refused saying what the hell is the use of a van, if we can’t take the kids with us. Isn’t that the whole point of the van????? so I can go with them where they want to go. (Well what can I say) So we’re still confined to home, but with a little bit of patience and a little bit of luck hopefully another one will become available soon. We’ve got a couple of weeks grace period anyway, as the independent assessor who has to approve our choice of van is away on holiday.
As I’ve mentioned in a previous post, Bill and I have become quite close with a couple in Canada, Rick and Joan.We’ve learned recently that Rick’s condition has worsened dramatically. From their blog, Bill and I have learnt all we ever needed to know about MND/ALS. The highs, the lows, the “to do’s, the not to do’s” to “give this a try” it is a very informative blog if you suffer from MND/ALS it is also a strong testimony in faith, love and spirit. Some of their korero is pretty scary, in that they are facing the future practically and head on. Something that we as maori traditionally wouldn’t do. But if I’m being honest I find it fascinating, the strength of spirit it takes to make public their innermost thoughts at a time when most would be determined to push things aside and wallow is absolutely awe inspiring to me. So to Joan and Rick just wanted to say your little piece of “hyper space” has made the world of difference to Bill and I.
That’s all from the Gardiner residence this cold night, catch up again soon.
Erin
Monday, July 5, 2010
Double Blessing – Good things do happen sometimes.
Blessing number 1:
Quite a while back, when Bill couldn’t drive anymore, we gave his car to the boys. Wasn’t such an issue for us, I am within walking distance to work, our two youngest were on the bus route to schools etc. Then between the two boys they racked up a whole heap of fines, from speeding fines, to parking fines, to you name it they got fined for it…….Dang…..SO, I sold the car out from under them, paid off the fines and that left us carless. (Again, not really an issue then). The last couple of months have been pretty trying in terms of getting anywhere, mainly while Bill was in hospital, my neighbours (our cousins) gave us use of one of their cars during this period, bless them. Bill left hospital on the Wednesday and on the following Sunday while at the club, something crazy happened. Mums boss, who also happens to be a relation of ours rocked on in to the club, took me aside and told me she had brought my family a car…….I thought to myself, get outta here, those sorts of things don’t happen to us! Now, she had obviously had a drink or 10 lol, and I wasn’t really taking her seriously. BUT, while I was at work on Monday, the phone rang, it was my Mum telling me the car was ready to be picked up from the car dealers, NOW…. Well, I just about fell off my chair. I still wasn’t believing it, phoned our oldest son at work, told him what had happened, asked him if he could take the rest of the afternoon off work and to go pick the car up for us, I was too busy thinking I was dreaming the whole thing. An hour later, my family and I were sitting at home looking like stunned mullets at this gift that had been given to us… What do you say to people who just out of the blue do things like that, geez it’s been two weeks and I’m still pinching myself. Thank You just seems so inadequate.
Blessing number 2:
Just before Christmas we applied for a lotteries grant to purchase a mobility van with hoist for Bill. You guessed it…..this past week we were notified by the lotteries board that our application had been approved. GOBSMACKED! I picked the letter up from the mailbox, started reading it and by the time I got on to our deck I was doing a dance and whooping and spluttering and generally looking like an idiot, then I showed Bill the letter and honestly he almost, ALMOST jumped out of bed and did a jig himself…..lol. Good grief, from no vehicle to 2 vehicles in 2 weeks. We are still shaking our heads not believing what has happened. Nothing like this has ever happened to us before, and I don’t think it will ever happen quite like this again, but hell its put a smile on Bills face that makes it all worth while. Have started the hunt for the van which will need to be approved by a qualified assessor as being appropriate for Bills needs, and once the van has been approved then we need to do the modifications (fit the hoist etc). So not sure how long that process will take, but hopefully by next month sometime, Bill will have van and Bill will travel YES!
Just wanted to share that with you all, still can’t quite believe it. Have got to say that we’ve been visited by angels over the past several weeks, from our cousins next door,to mums boss (you know who you are) to the lotteries board and those who helped us put that application together THANK YOU!
The Gardiners