I think I'm just ready to surrender..I'm sick and tired of being sick and tired...nobody cares anyway
No help no financial no doctor no insurance..disa... - LUPUS UK
No help no financial no doctor no insurance..disability fight on and on forever
Hi! Share your ordeal! We might help you in some way Dont lose hope please
Can you tell us more? You sound desperate and we do care about others here so please do explain more about your situation.
Many of us do feel that way, especially when the disease is progressing.
There are lots of people here who have felt that way. The feelings aren’t permanent. Can you tell us what you’re dealing with? There are people here who understand, and care.
Please share
I can understand how down you can get when you have so much pain but please ask for help from this site it will encourage you to know you are not alone.
You are NOT alone!!! Please let us all help you. If nothing else we can chat with you and comfort you.
Sending hope
🌻💙☉
Please don't give up, not yet - we've all been there - and there are new medicines and procedures and inventions every single day. Can you tell us what's happening with you to make you feel so dreadful? Maybe we can hep? Or at least share . . .
Hi! I'm sorry you feel so down. Please share here these people are so lovely and helped to kick me up the bum and carry on with my fight when I just felt like giving up! Please don't give up we're all here, we care. xxx
It seems s though you are crying out for help. This is a safe caring place to do that. Please don’t suffer in silence. There are many here that would like to help.
I care..we all care xoxox
Hi Dcharpia,
Would you like someone to speak to? We have a list of LUPUS UK Contacts who you can chat with over the telephone. These contacts are volunteers who mostly have lupus themselves; they are not medically trained but are there to offer support and understanding. If you would like a contact to speak to, you can email me at chanpreet@lupusuk.org.uk with your name and address.
We published a factsheet that contains services and support helplines which may be of interest to you: lupusuk.org.uk/wp-content/u....
If you would like literature regarding ESA/PIP/Work/General Benefits i.e. reconsiderations, appeals and the support available to you, you can email me.
Please do not lose hope, you have received a number of caring replies showing you that you are not alone! We are all here for you.