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Ice Cream diet 🍦

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    Ice Cream diet 🍦

    I know that eating is tricky for many, and PEG is what many have, but I thought this would be fun. Personally, I’m getting A LOT of extra saliva and coughing on water and my own saliva. I am struggling to have an appetite, and skipping meals… but Tiny Lady mentioned her plan of an ice cream diet and that made me smile!
    I thought this topic could be for anyone who wants to post something decadent/delicious that they want to eat, plan on eating, ate or would eat if they could…
    the name and/or a picture.
    Me first: Homemade (not by me 😹) butter tart

    #2
    I had trifle today. No one else in my house likes it, so I never have it. It was on offer in my local co-op, I only went in to use the cash-point! It was enough to serve four people and I'm going to eat it all myself πŸ˜‹ ......maybe not in one sitting though!
    Started limping 2017, diagnosed August 2021. Wheelchair user and reduced shoulder function. Trying to be positive 😺.

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      #3
      Amazing, Tabbycat! I love trifle!
      Here is my butter tart that I just polished off πŸ€—
      Attached Files

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        #4
        AngieCanuck I wasnt familiar with a butter tart so just googled it, it sounds delicious.

        Google describes it as quintessentially Canadian, melt in the mouth and deliciously gooey.
        Last edited by Tabbycat; 22 March 2022, 21:05. Reason: Pressed post before I'd finished typing!
        Started limping 2017, diagnosed August 2021. Wheelchair user and reduced shoulder function. Trying to be positive 😺.

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          #5
          AngieCanuck there’s a Butter Tart Fest in Paris, in May!

          Tabbycat you need to really like sweet to enjoy them, but mmmmmm!

          I just want the opportunity to go out for sushi. 😒
          Diagnosed December 2020 with lower limb onset ALS, now involving hands and arms.

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            #6
            two words. Angel Delight.

            Ticks all the boxes for me, calorie dense, easy to eat and reminds me of my youth.

            perfick.

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              #7
              richcrocker Yes! I love Angel Delight too.
              What's your favorite flavour?
              Started limping 2017, diagnosed August 2021. Wheelchair user and reduced shoulder function. Trying to be positive 😺.

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                #8
                Tabbycat butterscotch.

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                  #9
                  Originally posted by richcrocker View Post
                  two words. Angel Delight.

                  Ticks all the boxes for me, calorie dense, easy to eat and reminds me of my youth.

                  perfick.
                  Now you’re talking πŸ˜‹πŸ˜‹πŸ˜‹
                  Foxes Never Quit πŸ’™

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                    #10
                    I have never had Angel Delight, so I’ve ordered butterscotch flavoured angel delight from Amazon. I like puddings so I’m excited to try it πŸ‘
                    This morning, I’m having one of these with my morning coffee
                    You do not have permission to view this gallery.
                    This gallery has 1 photos.

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                      #11
                      AngieCanuck - my physio recommended Ben and Jerry's Phish food ice cream... so I want to try that. But in non ice cream news... I tried to eat a chocolate croissant for breakfast on mother's day. Big mistake - just couldn't stop coughing afterwards.

                      Back to the ice cream then....

                      BTW- I'm unusual because really not keen on Angel delight.
                      Diagnosis confirmed Jan 2022 (age 46) after several years ignored/ misdiagnosed.

                      Symptoms began in left foot 2017. Now mainly left side, speech and some loss on right side too.

                      Unable to walk unaided (powerchair user), poor speech, left hand behaves like a drunk toddler but generally positive and determined.

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                        #12
                        TinyLady ooh now you're talking. I'm not a big ice cream eater but can't resist Phish Food, it's my favourite flavour.
                        Started limping 2017, diagnosed August 2021. Wheelchair user and reduced shoulder function. Trying to be positive 😺.

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                          #13
                          Tabbycat I will have to get some then and report back to you and my physio 🀣
                          Diagnosis confirmed Jan 2022 (age 46) after several years ignored/ misdiagnosed.

                          Symptoms began in left foot 2017. Now mainly left side, speech and some loss on right side too.

                          Unable to walk unaided (powerchair user), poor speech, left hand behaves like a drunk toddler but generally positive and determined.

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                            #14
                            Originally posted by TinyLady View Post
                            BTW- I'm unusual because really not keen on Angel delight.
                            Me neither - as a child I used to trade mine 😍😍
                            ​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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                              #15
                              Custard and stewed apples have been a hit with Thomas.

                              Choc Ices

                              Giant chocolate buttons

                              Obviously ice cream

                              But his sweet tooth seems to be lessening.

                              He has even gone off alcohol free beer, went AF at start of onset which is a shame.
                              Donna

                              Carer for husband Thomas, diagnosed with MND of Fail Arm Type in July 2020.

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