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    Hi. I can’t find how to add a signature please.




    Husband, Nigel, diagnosed with ALS in July 2019. We live in Spain and the medical care is superb. Nigel currently taking Riluzole. Tried acupuncture/Chinese medicine and bee venom (privately), but not helpful. Had stem cell therapy 6 months ago, but no improvement so far.

    #2
    Originally posted by Puddy View Post
    Hi. I can’t find how to add a signature please.
    Hi Puddy,

    To create a signature:

    Go to the very top of the page, on any page in the forum.
    There are several lozenge-shaped buttons labelled Puddy, Notifications, My Profile, Settings, Register, Login.
    Select Settings
    A page will come up which has, on the left, a column of several boxes labelled: My Messages, My Subscriptions, My Settings.
    In the My Settings box, under My Profile, the fourth item in the list is Edit Signature. Select "Edit Signature" and away you go.
    Dina

    Trying to keep positive, but not always managing.

    Comment


      #3
      Hi Puddy;

      Many of us use the signature to write a message instead of our names, horses for courses.

      Dina has done both in different colours.

      Love Terry
      TB once said that "The forum is still the best source for friendship and information."

      It will only remain so if new people post and keep us updated on things that work or don't work and tips.

      Please post on old threads that are of use so that others see them and feel free to start new subjects and threads.

      Comment


        #4
        Thanks - have added signature. Let's see if it works.




        Husband, Nigel, diagnosed with ALS in July 2019. We live in Spain and the medical care is superb. Nigel currently taking Riluzole. Tried acupuncture/Chinese medicine and bee venom (privately), but not helpful. Had stem cell therapy 6 months ago, but no improvement so far.

        Comment


          #5
          Yep, it works perfectly!

          Lovely pic too
          ​Diagnosed 03/2007. Sporadic Definite ALS/MND Limb Onset.
          Eye gaze user - No working limbs - No speech - Feeding tube - Overnight NIV.

          Comment


            #6
            Thanks Ellie - the photo of us is of Viking Day at the local tavern. They cater for every nationality. The night pic is outside our little casa.




            Husband, Nigel, diagnosed with ALS in July 2019. We live in Spain and the medical care is superb. Nigel currently taking Riluzole. Tried acupuncture/Chinese medicine and bee venom (privately), but not helpful. Had stem cell therapy 6 months ago, but no improvement so far.

            Comment

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