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    Hello everyone

    My name is Tina I'm new on here. My left foot started catching in October 2019 causing me to fall. I was diagnosed May 2021. I saw an MND professor a couple of months after for it to be confirmed. I have PMA progessive muscle atrophy. I have left foot drop and weak legs. Use walker indoors but need wheelchair with support when I go out. Wondering what the future holds but trying to staying positive. Its great to see I'm not on my own as it is a lonely disease. There are others out there with the same problems.

    #2
    Welcome to the club Tina! A place none of us want to he members of but the forum is a place for friendship and support and fun and a lot of information. I was only recently diagnosed. Mine started with right foot catching on floor and balance problems. We are here for anything u need. Take care and am sorry u find yourself here. Xx
    Diagnosed June 2022. Confirmed MND. Limb onset. Symptoms started November 2020.

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      #3
      Hello Tina and welcome to the forum although I am sorry that you find yourself here 😔

      I look forward to seeing you around in some of the threads, James x
      Foxes Never Quit 💙

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        #4
        Aww thank you guys it's so good to speak to others in the same situation. I've been looking through some of the posts and there is a lot of support for each other which is great. Seems to be more and more people being diagnosed with this cruel disease. 💙 xx

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          #5
          A warm welcome to the forum, Tina.

          Now you've found us, you'll never feel alone in coping with your MND-PMA again 🤗

          As well as support and advice, the forum is a safe place to have a weep or a moan, as well as having an all important laugh, take part in a quiz or recommended a film or book.

          Love Ellie xx
          ​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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            #6
            Hi Tina and a very warm welcome to the forum.

            I'm so sorry for your diagnosis but I'm glad you've found us. This is a good place for support and friendship from people who really understand.

            Love Debbie xx😘🤗

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              #7
              Thank you so much Debbie ❤️

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                #8
                Thank you so much Ellie ❤️

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                  #9
                  Tina welcome to the forum. I too started with foot drop and falls.
                  Started limping 2017, diagnosed August 2021. Wheelchair user and reduced shoulder and hand function. Trying to be positive 😺.

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                    #10
                    Tina welcome to our forum. Sorry you have to be here but like others have said it’s a great support to us all.I’m a carer for my husband. Diagnosed Oct 17, five years this October. Still walking but very frail. Still eating and swallowing but mashed up food. So all in all, not doing too bad under the circumstances. Take carexx

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                      #11
                      Welcome to the forum Tina, sorry to hear about your diagnosis but as everyone has said there are lots of friendly and supportive people here willing to share their knowledge and experience.

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                        #12
                        Hi Claireflo thank you so much..yes I can see by the posts makes you feel better knowing your nit on your own with this horrendous disease xx

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                          #13
                          I'm still trying to find my way around this site but thank you to everyone that took the time to post to me it means a lot ❤️

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                            #14
                            I am in the same bot i af the same ny left foot is numb and my right foot is gated worse

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                              #15
                              Sorry for your diagnosis but welcome like others have said here you will be able to find a wealth of information plus you can have a good old moan or anything else as we battle this terrible illness. X Love and light to you 😁

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