November 29, 2018 at 1:18 pm #14560
What Is the first thing you would do if you were free of MS? I would run around my house and scream with joy!! What would you do?
December 6, 2018 at 7:32 am #14657
My daughter asked me this question and I told her if I had one day free from ms I would go ice skating and then dancing. Not that I was ever very good at either, but I think I would fly around with reckless abandon, and skate away from all these people in my life who’s lack of confidence in my abilities has left me more timid and cautious than I like. As far as the dancing, just turn it up LOUD!
December 6, 2018 at 10:06 am #14663
That sounds wonderful, Cynthia! 🙂
December 6, 2018 at 1:57 pm #14669
I’d sleep through the night!
December 6, 2018 at 4:19 pm #14671
Get another dog or two and walk, walk, walk with them…
December 6, 2018 at 4:56 pm #14676
Ed and Jackie, Both ideas sound great!
December 7, 2018 at 7:13 pm #14689
I’d go hiking with my kids!
December 7, 2018 at 7:47 pm #14691
Perfect idea, Carla!
December 7, 2018 at 10:36 pm #14692
I would walk, run and climb a tree, get a job, earn some money and feel productive. But that’s not going to happen. However, if my knee operation is a success and I have no pain, I would like to think I would take a part time sit down job. Never had a sit down job before, kinda have to now. All my other jobs have been phyiscal. I am pretty good on computers, once I know what’s required of me, I can work miracles.
December 29, 2018 at 5:12 pm #14981
I’d take a walk around the neighborhood and take in the sights and fresh air, but when it gets warmer, I’d go to the beach and just walk along the shoreline. Would love to get back onto a beach.
December 30, 2018 at 2:04 pm #14984
January 2, 2019 at 11:27 am #14991
I was again asking myself this same question this morning….only putting the question as ” if I was granted one wish, what would it be…”
I was pondering over the answer of which one of two would I choose,…
1) as my life is now but take away my PPMS so I can get out there and walk another dog or two as I once used to to do..
2) put back the clock ( years ) to before MS, when I lived at my last address and still had my three darling beloved fur babies, only this time I would not waste any number of days with them…
Then after some tough deliberating I then came to my final answer of…
put back the years and relive my life in my then healthy body with my darling three dogs, where I would vow to make the most of every day and opportunity that I missed or neglected with them when I had them, even if it meant I would still have to face those dreaded days of having to say goodbye to them over again, now that was the main reason I was deliberating on my answer, I couldn’t put myself through that again, the saddest periods of my life..
Have to admit this would be a tough one as my first instinct and answer was to get rid of my MS so I can get on with the rest of my life…of course I would love to be offered the two wishes…of course neither will ever be a reality..
January 2, 2019 at 12:31 pm #14992
Just want to add…I was sitting on the sofa looking at the dogs three ashes boxes and photos on the sideboard when I was making my choice…have to admit they would have loved it where I now live, no roads, no traffic, just hills and valleys…and so would I love it it I didn’t have this d***n MS..As I posted above, I would get outside and walk, walk, walk…
- This reply was modified 11 months, 2 weeks ago by Jacqueline.
January 2, 2019 at 12:40 pm #14994
I am so sorry for all of your loss, Jackie. I can feel your pain through your writing, and the deep thought that went into your decision. It made me consider my own life and what I would do.
As much as I would like to see my husband again, and redo a lot in my life, I wouldn’t go back. I would stay where I am, and rid myself of MS. I do believe I will see my husband again someday and that you will see your beloved dogs, as well. So that gives me comfort.
Thank-you Jackie for posting such thought provoking questions!
January 2, 2019 at 12:45 pm #14995
Debi..yes, I have told the person ( man ) I live with that whatever happens I want my ashes laid to rest back home, somewhere near trees and birds and the three dogs ashes to be scattered with me…
As I said, this is a tough one, as the more I think of this question, the more I am leading to whats in the past must now stay in the past…it is the future now that we must concentrate on, and that means I may change my mind and go with the logical option…my chosen wish of making my PPMS disappear for ever so i can get on wit living…eve though living now would be empty without my three babies, my dogs were my life…
But of course we know the thought of being granted any wishes would remain as just a pipe dream…
- This reply was modified 11 months, 2 weeks ago by Jacqueline.
January 2, 2019 at 12:49 pm #14996
Sounds perfect, Jackie!
Yes a dream, it’s good to dream and imagine! Most of all to have great memories is the best!
January 2, 2019 at 12:55 pm #14998
Debi…let us all with MS make 2019 a year to remember, and all for the right reasons…let us keep positive to our future and savour every good minute, hour, week, month….As we know only too well, life can change in a blink of an eyelid, as it once did for us…One minute we were healthy, the next we were told those devastating words of…” sorry to have to tell you but you have MS …”
January 2, 2019 at 1:01 pm #14999
So true, Jackie!! I’m with you, 2019 will be a great year!!
January 2, 2019 at 1:58 pm #15002
Debi…there is no reasons why it cant be, I believe their is still better things to come…hold onto those thoughts, dreams and images…
February 13, 2019 at 10:32 am #15939
Travel to Australia and visit my daughter & son-in-law.
February 13, 2019 at 12:24 pm #15941
That sounds wonderful Amy!
February 13, 2019 at 3:32 pm #15944
Not the first thing I would do but today got me thinking….I now go to a weekly seniors afternoon bingo..only been a member three weeks but I am noticing one by one from our table of six they are taking it in turns at our half way break on going up to order and bring back the tray of six cups of teas and biscuits..Now there was a time I would have been one of the first to offer to do my share, but I will have to sit this one out as our rollator’s are moved to make way for people to walk through the gangways, and I already struggle enough getting up and manoeuvring myself out to the corridor visiting the loo, I need both hands to steady myself on everyone’s table as I pass by, then both hands as I hand walk the wall corridor, so carrying a tray full of six cups of tea is a definite no, no…We dont realise just how much MS has taken away from us, all the simple things we took for granted that we cant do anymore…MS just makes one feel so useless…
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