Because of the meds we take it's obviously a good idea to keep well hydrated, but I must confess I often simply forget.
In this hot weather, it's even more important, so I thought I'd share a handy bottle the RA nurse recommended on a recent appointment (she had it on her desk, swears by it). I've since found others in a range of colours and slightly cheaper but this one is BPA free.
Thanks for the reminder, although I do drink plenty. It's gonna be hot later today.
Even when it’s not this hot I keep a litre lidded jug of water/squash on my kitchen work top.
Every time I go into the kitchen I remember to grab a glass......as you say dehydration is bad for everybody....not just those with AI diseases.. ...especially when taking string oral medication.
Glugg away folks!
That's a good idea and I am going to order one in pink.xxxx
Seems very small! Is it about 500ml? I drink far more than that in a morning or afternoon....even when it’s not hot.
But yes, good reminder.
It's actually 900ml, which you're supposed to drink by 1pm, then re-fill again.
That makes more sense....think I’ll stick to my smaller bottles tho’ as easier to carry around.
Staying at home... still and Tocilizumab arriving on Friday
Do your doctors have different attitudes towards staying on prednisone?
Staying logged in to nras site.
Hips, back or bum? Post meno, RA or OA or just getting near to the big 50?
