I'm glad that you've had a good time Dina.
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Originally posted by Hayls View PostMy good news well, I think it’s hilarious but I think it’s my EL as it is still causing havoc, I’m finding new things I CAN’T do everyday but the best one yet is Eye Spy) I get so overwhelmed when I think I have the answer, I’m hysterically laughing to the point I can’t breathe or use what little use of my arms I have yet and I’m crying with laughter, I realised this after being stuck in a traffic jam in a car park for an hour and 40 minutes, it had everyone entertained at least
)
It was lovely to hear from you yesterday. Your post made me chuckle and it brought back happy memories of playing I Spy during car journeys with my family when I was a child. And sometimes we played it outside the car, when the car had broken down and we were waiting for the AA! (it might just be my imagination but I don't think cars were so reliable in the 1970's?? LOL).
I have played I Spy more recently though.
Last Summer, I was having lunch with a friend outside the cafe at our local park, when she said:-
"I Spy with my little eye something beginning with c i "
"c i what?" I asked, and she replied
"c i ate the last doughnut!!" LOL
Then it was my turn ...
"OK, I Spy with my little eye something beginning with i c "
"i c what?"
"i c a b buzzing around the sugar on your knee - and, watch out, because i c a q as well!!"
"I think I know? - is it the q for the ladies' loo?" LOL
"No, because I Spy that there is only one lady waiting - and that doesn't constitute a q! But I do Spy a very long q of ants, that goes down all the way down to Australia, and it starts at your very sugar-laden can of 7UP!" LOL
I hope you and your husband are having a lovely day.
Love,
Kayleigh xLast edited by Kayleigh; 10 November 2019, 18:49.
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My Good Thing today is that I had a sublime massage this afternoon
Feelin chilled, warm and can smell the essential oil still on me.
Hope everyone is managing to keep warm and safe.
Love Ellie.Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Good for you Ellie. I don't like oils on my skin but an actual massage sounds great. We've had our heating on for weeks and I have a couple of fleece blankets near to me that I use often for my easily cold legs. Lynne xALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my ballance.
I'm staying positive and taking each day as it comes.
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Originally posted by Gillette View PostHi Ellie
It sounds wonderful. I could do with one myself.
Lynne, I've been really cold since I came home from hospital. Our heating is on high all day long.
Could it be that hospitals always seem to have their heating on at 40 degrees centigrade or was it the firemen you saw outside the hospital that raised your core temperature?? LOL
Talking of those firemen, I have tracked one down and as soon as he has finished 'warming up' Ellen's friends, he will be round to yours' to give you one of his very warming 'hot stone' massage therapies (apparently they never fail to 'light your fire' or 'melt your butter' or 'warm the cockles' - and, apparently, they are going like hot cakes!) LOL.....
My opinion might be a 'hot potato' or even hotly contested.... but I would say this is 'One for the ladies!' (But I promise these hot flashes shouldn't be too hot for anyone to handle).!!! .... LOL
http://https://m.youtube.com/watch?v=ydt2GqFThzs
Love,
KayleighLast edited by Kayleigh; 13 November 2019, 19:40.
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Hi Kayleigh,
Your post of the American chat show host Ellen with the fireman reminded me of a more serious interview she gave. You can feel the emotion she and the interviewees were experiencing. I wish we had more media led campaigns in the UK to raise awareness and hopefully funding.
https://youtu.be/KDvuRR-UiGY
Love,
BarryI’m going to do this even if it kills me!
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Thank you for sharing that interview with us Barry. A very brave firefighter indeed and to receive his diagnosis at such a young age makes it even more heartbreaking.
It's wonderful that Eric Stevens and his wife were brave enough to go on TV to raise awareness of MND and the Axe ALS Campaign. It was also great to hear that Ellen was able to arrange some financial support for them as well.
Love
Kayleigh x
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