Ive just received my letter advising my DLA will stop and i need to apply for PIP. Has anyone with diffuse scleroderma recently been through this process? Any advice?
Change from DLA to PIP: Ive just... - Scleroderma & Ray...
Change from DLA to PIP
![Lyyders profile image](https://images.hu-production.be/avatars/3a72542ae9cb25729a4691dff7338807_small@2x_100x100.jpg)
![Lyyders profile image](https://images.hu-production.be/avatars/3a72542ae9cb25729a4691dff7338807_small@2x_100x100.jpg)
If you need help to complete your forms your local CAB can help. They know the indicators which make up the points you need to receive an appropriate award.
I am still waiting for my PIP result whether I will get it or not. I have Scleroderma and Raynauds. I have noticed that they are starting to realise our illness. I really could do with the help. I hope you get it. The thing I find they are not doctors who assess you and they have not got a clue what pain we suffer.
The PIP I tried a couple of years ago. But I found the test was a lot more harder this time. I again asked for them to come to my house for assessment. Put this time he had a right bag of tricks eye tests you name it.
Good luck
Liz
I recently applied for esa and pip winning both how did you get on
Test was very daunting at times