I hope you are back with us soon. It is awful that you are having such a horrible, horrible time and that things have got so much worse. I do hope that this awful trauma turns out to be the first step towards rebuilding a much better life. There was no way things could have stayed as they were.
Thinking of you.
Alison
x
Good Luck, I’m so sorry things have gone so badly for you. I hope your new life will improve no end for you and your daughter. Teresa xx
Hi I need help, I have relapsing remitting ms I have had the disease for 13 years. I have claimed dla for maybe 8 years of those 13 I have today received my pip letter saying I need to make a claim for pip. Can I have some advice please. What sort of things are asked, do we get a physical assessment how long does the process take? I have so many questions with so little time. This isn’t helping my symptoms what so ever I suffer from agonising pain from nerve damage amongst a list of other things why do they put us through the stress of all this?
Hello,
Can you say what sort of help you are looking for?
- Is it about care you need?
- Medical advice?
- Financial help?
- Something else?
Best wishes,
Anthony
Hi there
I was diagnosed with MS relapsing remitting in April, currently taking copaxone which I find is really helping me, my symtoms are hardly noticeable. Four days ago I experienced my first common cold which is still on going. was it common for others that their symptoms came back? before taking the medication I used to experience a tingling in my foot and leg which went away when taking copaxone. I have now noticed this has returned when the cold came.