Viewing 12 posts - 201 through 212 (of 212 total)
  • #75922
    Re: Say “hello” here

    Hi Catatude

    To blog on the Trailblazers website I recommend the following:

    1) Log in to website with your username and password

    2) Go to ‘Get Campaigning”

    3) Go to “Blogs” on the left hand menu

    4) You should see “Add a blog post”

    5) Add your blog

    Hope that helps, if not drop me a line at trailblazers@muscular-dytrophy.org

    bobby
    Participant
    Posts: 7
    Joined: 13/10/2010
    #75923
    Re: hello valerie

    my name is linda i have been likened to mitochondrial myopathy when i was 36 i am now 53 and no closer to a firm diagnosis this disease affects my life (what diease dont ) and can feel very frustrated with doctors lack of understsnding . this is the first time for me to be on this site so dont know my way round yet i am also new to computers having only just received it as a xmas present from my children but i had to say hello to a fellow sufferer also for the 1st time dont know anyone with a muscle condition i sound pretty green dont i never mind linda :lol:

    lindasloc0001
    Participant
    Posts: 13
    Joined: 01/03/2011
    #75924
    Re: Say “hello” here

    Hi Linda
    Welcome to the forum
    What lovely children you have got to get you a computer for Christmas. I’m sure you’ll soon find your way round it. It must be very frustrating not to have a confirmed diagnosis. Is your consultant still looking into it for you? How are you affected by MM?
    If you would like to compare notes PM (private message) me your email address and we can chat.
    Take care
    Val

    Valerie
    Participant
    Posts: 166
    Joined: 15/09/2010
    #75925
    Re: Say “hello” here

    Hi Linda, welcome to TalkMD.

    I am sure you’ll pick things up as you go on the forum but if there’s anything you or others are not sure about, AMG has produced some great guides to how it all works which you will find in the Hints and Tips section.

    Best wishes

    Sarah :)

    A learning experience is one of those things that say, “You know that thing you just did? Don’t do that.” - Douglas Adams

    sar78 sar78
    Moderator
    Posts: 2,246
    Joined: 05/03/2015
    #75926
    Re: Say “hello” here

    Hi Linda, welcome to the forum

    Vicki
    Participant
    Posts: 1,015
    Joined: 05/03/2015
    #75927
    Re: Say “hello” here

    hi vicki thanks for the welcome :D linda

    lindasloc0001
    Participant
    Posts: 13
    Joined: 01/03/2011
    #75928
    Re: Say “hello” here

    hi to everyone who welcomed me into this forum and thankyou for doing so i have felt very isolated being the only one i know with muscle disease :roll: i know im not the only one! there are quite a few of us around and also some upsetting tales to be told. thankyou valerie for your message when i know how to send my e mail privately to you i will just hope you dont regret it :lol: ihave loads of interests (even tho i cant do them so much) i like having a laugh playing darts crosswords t.v but not soaps talking etc linda x

    lindasloc0001
    Participant
    Posts: 13
    Joined: 01/03/2011
    #75929
    Re: Say “hello” here

    @lindasloc0001 wrote:

    ….. when i know how to send my e mail privately to you i will just hope you dont regret it :lol:

    Linda, I have posted some FAQ, walk through type threads for novice board users. They are in the “Hints and Tips” section. Here is a quick link to the one for sending private messages Private Messaging The easiest method is the last paragraph of the very last post.

    Let me know if you have any problems or confusions, I will gladly help and tweak the help guides.

    I'm always the animal, my body's the cage

    I blog about nothingness www.amgroves.com

    AM
    Participant
    Posts: 4,751
    Joined: 05/03/2015
    #75930
    Re: Say “hello” here

    Hi,

    I’m Lisa and I’ve just joined the Muscular Dystrophy Campaign as Senior Policy and Campaigns Officer. I’m working in the Policy and Campaigns team, splitting my time between working with the Muscle Groups and campaigning nationally to make sure the voice of people with muscle disease is heard by government.

    I just wanted to pop by and say hello – I look forward to talking to you on this forum and hopefully meeting some of you in person at an event soon!

    Lisa

    lisajames
    Participant
    Posts: 2
    Joined: 04/03/2011
    #75931
    Re: Say “hello” here

    Hi everybody!
    I have Limb-Girdle type 2a MD/Calpainopathy from a deletion mutation.
    I would be very interested in hearing from anyone who has found anything that helps in any way.
    I would also like to meet some people with LGMD2a and compare notes on progression and managing symptoms.

    Chagrin
    Participant
    Posts: 130
    Joined: 04/03/2011
    #75932
    Re: Say “hello” here

    Hi Chagrin and welcome.

    There are a few members here with Limb Girdle who I am sure will make contact.

    I am glad of the travelling I did in my teenage years and the tall ship sailing I did in later years, those memories are precious.

    I'm always the animal, my body's the cage

    I blog about nothingness www.amgroves.com

    AM
    Participant
    Posts: 4,751
    Joined: 05/03/2015
    #75933
    Re: Say “hello” here

    A big hello and welcome to Linda and Chagrin.

    Paul58
    Participant
    Posts: 85
    Joined: 05/10/2010
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