Hi, my name is Ricky

PharaohMan86
PharaohMan86 Online Community Member Posts: 2 Listener
Hi I severely suffer with M.E for 7 years, I'm always very tired & spend most of my time asleep, I can't do any activities because the slightest thing is like running a marathon, mentally I'm really struggling, nice to meet everyone 

Comments

  • chiarieds
    chiarieds Online Community Member Posts: 16,736 Championing
    Hi @PharaohMan86 - & welcome to the community. I'm sorry to read you have M.E. as this seems a very difficult condition to live with.
    Have you discussed the mental aspect of this with your GP? Hopefully they may be able to help.
    It's good to 'meet' you too, & I'm sure you'll find the community both helpful & supportive. :)
  • PharaohMan86
    PharaohMan86 Online Community Member Posts: 2 Listener
    Thank u guys, I'm just hoping to meet people on here who suffer what I go through & for any advice & also to make friendships with people who are the same as me, yes I hav been on at my GP but she is pretty useless, also been to class sessions 5 years ago but I also found it useless lol, nice to meet u guys 🙂
  • MissMarple
    MissMarple Online Community Member Posts: 188 Empowering
    Welcome to the community @PharaohMan86 I'm also a member of the sloth club, need to nap after breakfast.  :smiley: Hope you'll find advice and friends here. I know that even getting online can be difficult when one is exhausted.
  • Dempseym
    Dempseym Online Community Member Posts: 36 Contributor
    Hi @PharaohMan86,
    Welcome to the community.   I am glad you have joined our community, welcome!  It must be very difficult for you but we are here for you no matter what your disability throws at you we are here for you. 

  • [Deleted User]
    [Deleted User] Posts: 0 Listener
    Hello @PharaohMan86 I would like to welcome you to the community. 
  • Danielle_2022
    Danielle_2022 Online Community Member Posts: 265 Empowering
    Morning @PharaohMan86,
    Thank-you so much for taking the time and using up some of your energy to tell us a bit about your story here. I have a few friends with M.E and their experiences sound so similar to yours, so I wanted to reassure you that you're not alone. I'm also really glad to see that this post has found a few people with M.E from the community, too. I hope that you'll have a chance to connect and feel less isolated. I know that there has been so much difficulty around the NICE guidelines for treatment, which has made it harder for a lot of people to access the right support, too. If you aren't having much luck with your current GP, it may be worth looking to see if it's possible for you to get an appointment with someone else. As ever, everything is a fight & its one that can be exhausting at the best of times, but I do hope that you have support from family/friends with it all. We'll do whatever we can for you, too. Keep in touch, whenever you're able :)