[numbfoot]

Haven't been on here for a while.
With PN progressing into my hands I am now having trouble holding on to things.
Not through lack of strength as yet, I think it's more that I am not exerting enough pressure. It tends to feel like they are slippery. I assume I am not the only one with this problem & was wondering if there is something I could apply to my hands to give them more of a grip. Some sort of cream or spray that sets slightly tacky perhaps. Unfortunately I use a touch screen mobile phone in the course of my work & gloves dont work.
Also the temperature control of my hands has gone nuts. In the winter they feel frozen & in summer they burn. I find myself sitting on them a lot.
My feet are the same of course but I have taught myself to ignore them.