@HMbadwalker 

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HMbadwalker

Feeling useless

I am new here and have never really spoken about my ms. I was diagnosed about 20 years ago and until about 6 years ago (on Avonex) I was able to lead a fairly normal life with only occasional relapses, general fatigue etc. After that my balance and walking got much worse. I am now taking Aubagio and my general health is fine but my walking is limited. I am determined to keep going as I dread more than anything being totally unable to walk. I have lost confidence when I am out as I am scared of falling. Having always been independent and active I now feel as though I am a completely different person! When I try to explain this to people they say things like “oh, we have all changed” - I just want to reply “yes, but you can still walk and lead independent lives!” I feel very isolated and quite resentful when I realise the limitations of my life. I have a very supportive family and because of them I have to keep going, however I don’t think that they really understand quite how miserable I feel sometimes and how I hate being pitied etc. I am sorry to have ranted in a self pitying way, but hopefully people here will understand.
@watsoncraig

Hi, Vent away. Loss of independence is a big worry as it’s one of the things we strive for growing up but those who love you will understand

@Lisa_Morghan

Yes that's what this MS site is for get it out !!! Pretend your in a " Jojo" punch the bag hit a pillow scream..... I'm Lisa MS has litterly taken my family "Mother Sister Me Lisa" all have been diagnosed with this ugly gross disease!!! I'm sorry for this that you have this.... Hang tough stay positive and keep writing ✍👀👌💪⚘