[quote=“QoS”] Robert, sorry to hear of your diagnosis… Sounds like you’re switched on and prepared to tackle PPMS, best wishes on your journey. [/quote] Thanks Qos,
Yes your right I am more switched on than I was when I was diagnosed. Since then I have decided that I have got this disease and there is nothing I can do to stop the progression. But I will fight it by guts and determination to prevent me deteriorating and being confined to a wheelchair.
So I spoke to someone on the ms society helpline who sent me all the booklets and leaflets on ppms which I read.
I then searched online for ms support in my area ms society is to far away to travel, all other support is in Glasgow and the best one I could find was revive ms support.
So now I am in a much happier place than before and I urge anyone who is just diagnosed who is in limbo and thinks the world is over. Take a step back call the ms society helpline, get all the booklets you require and everything will become clearer for you to.