Hi all, just a update on my pip claim, i put my claim in back in may this year and had a home visit 2weeks ago, on the day of my visit i was suffering really bad. I had a very nice lady come to see me, i could hardly get my words out that i needed so she asked did i want to carry on another day..we carried on and my husband took over answering the questions with me...consultant says my lupus is really not under control and my levels are going crazy so they added azathioprine to the mix, along with my steriods etc and the other bag fulk of drugs us fello lupies have to take to be able to make it through the day..well im waffling now lol so back to the reason for my post..i went to work thismorning, my body was maxing out and had to return home, feeling upset that im struggling to cope and feeling at a loss, 2 mins in the house and the brown envelope comes through the door, heart racing i felt so scared to open the letter, you know when you have been hoping for some good news but your affraid to get your hopes up just to be let down..well after opening. ......THEY AWARDED ME IT OHHH THANK YOU LORD!
I have been awarded the standard rate living element and the higher mobility part.
I would like to say a massive thank you to Paul from Lupus uk and your team who have sent me out paperwork to help and guide me understanding how to explain your condition in the way the assesers understand, thank you all on lupus uk for even though i dont know you in person, knowing there is a place we can ask questions, get advice and emotional support has and is keeping me going...
If there is any tip or helpfull information from my assesment who was capita is, tell them in as much information about each health problem. Try to think your explaining how things are to a loved one and be honest in how being so ill affect you, there more examples of this the better as they can imagine you doing this and how you cope if you try and the effects it leaves you with..xxx sorry if ive waffled on