these changes been a learned spiritual journey as well and what with these claims and things they can really take it out of one. I realise that money is quite a decision but when it a genuine claim I kinda guess its ok to claim for it but never mind before I ramble on about how the world should be ty all very much. Especially to foggy for her lovely concerns but to reassure you I walk around my flat (with crutch I use my mobility bike twice a day to take my dog out , couldn't do it otherwise. Overdo it regularly and that's why I flare every week and end up taking more meds just for that day though and I do bend down a little to often which I know does more damage but I do use my crutch or sideboard or even the correct lift through my left leg to prevent this . Im a large lady but not lazy I've always had horses and ponies all my life enjoyed the out doors and took many interests but this illness like so many of you I've read about now struggles everyday to keep some normality in my life ty all for your reply's this illness isolates me from other people but I know you guys just know. Its real comfortable in my soul. The fog is a real bitch for me my long-term memory is fantastic but my day to day and through my day is lousy and frustrating and morale robbing but I've accepted a lot better since meeting fibro peeps ty all again for your wonderful sharing of your illnesses ty xxxxxxxxxxxx
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