H.O.P.E. (Hold On, Pain Ends)

“The best way to not feel hopeless is to get up and do something.
Don’t wait for good things to happen to you.
If you go out and make some good things happen,
you will fill the world with hope,
you will fill yourself with hope.”
(Barack Obama)

It has been a bit of a hectic, but a great time to write lately. Two bits of fantastic news came my way in regards to my writing, and I’ve been over the moon since.

While I have not posted regularly on my own blog, The Irish MS society invited me to voluntarily join their blogging team. Needless to say, I was delighted to hear they wanted me to join their ranks.

It’s an enormous honour for me to be part of the blogging team. The society’s commitment, care, understanding and continuous support not only to myself, but to countless others, has been and continues to be beyond words.

Such is the admiration and love I feel for the society that I already sang their praises in a previous blog post (for which I apologise if I annoy you reminding you of this).

You can find my introduction blog post on the MS Ireland website is listed here. They will add future posts written by myself to their website, and I will provide links to them from my blog here. In the meantime, please check out their website regularly for more posts by other MSers and to find out news from the world of MS.

Blogging for them doesn’t mean I will stop posting on my own blog, though, so keep on coming back here to catch up and read as you please.

As far as the other piece of great writing news, as the old adage goes “Watch this space!”

If you want to financially support MS Ireland, please go here.

For more about the MS Care Centre, please visit this site.

For more on the MS Ireland blogs, please go here.

MS Infoline: 1850 233 233

© WVE and Ireland, MS and Me, 2011-2014. Unauthorised use and/or duplication of this material without express and written permission from this blog’s author and/or owner is strictly prohibited. Excerpts and links may be used, provided that full and clear credit is given to WVE and Ireland, MS and Me with appropriate and specific direction to the original content.

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2 Comments

  1. Well done my lovely, that is fantastic news, go girl. I have never had any support from anyone with my MS, Fibromyalgia, CMT muscle wasting and I’m kind of struggling. Living in a new area and I don’t know a soul. I plucked up the courage 2 weeks ago to contact my local MS Society, the lady took my name and details, she said to me “Ooh you used to be a teacher, maybe you could be on our committee” I don’t want to be on any committee at the moment I just wanted somebody to talk to, they never got back in touch after my initial query. I really hope not I will find someone soon. Happy Easter lovely lady, Su xxx

    Liked by 1 person

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