It's super tempting to exercise and do lots of things, but when I do try, I'm shown that I'm not as cured as I think I am but still 100% better than I was before if that makes any sense. I've been doing the O'Hara chair exercises 10 mins ever 2 days, I'd love to do it every day but I need to pace myself, as these ware me out and make me sore regardless of painkillers took. So instead of totally over doing it like I normally do, but pace and leave energies in reserve.
The Hypermobility has flared up in the shoulders, but I've read that the steroid can cause it too flare up and cause issues when patients are down and depressed too, so it explains it and gives me hope that it will settle down once the steroid eases out my system as well.
Well it's been 4 weeks post op now and time has admittedly flown by, with buying school uniform and planning the kids holiday. Oh and of course the riots too!
Found some amazing bloggers against the ATOS medical group, in a name and shame blog I've submitted by own atos story, and I've found help on twitter and forums. Get in touch with me if you want to know more, or need any help regarding the Atos medical assessments.
http://enchantednails@hotmail.com and I will endeavour to help in anyway I can.
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