I am new here!!!: Been diagnoised with... - LUpus Patients Un...

LUpus Patients Understanding and Support

3,425 members1,261 posts

I am new here!!!

5 Replies

Been diagnoised with SLE Lupus with kidney involvement for over 5 years...looking for some friends and support in this VERY HARD journey!!

Read more about...
5 Replies
lupus-support1 profile image
lupus-support1Administrator

Dear Amanda,

Welcome! I am sorry you have been suffering from lupus for over 5 years. I would like to invite you to register (free) at lupus-support.org/LuPUSMB at the LuPUS Message Board.

LUpus Patients Understanding & Support (LUPUS) specialise in free information and free online psychological support. Our forums are private and cannot even be seen unless a Member. I validate each registration to try and ensure there are no spammers!

If you have any problems, email me at: roz [at] lupus-support [dot] [org] [dot] [uk]

I look forward to talking to you.

Ros

lupus-support1 profile image
lupus-support1Administrator

I should have mentioned to try and choose an anonymous Username/Display name and please read the What is the LuPUS MB? forum.

With good wishes,

Ros

pattismith profile image
pattismith

I've also had that for 2 years now, obs had Lupus for years that wasn't picked up on hence severe kidney damage . I suggest you educate yourself as much as you can on the illness, that way we can understand more and get to know how our body responds to different situations and medications as everybody is different. Being part of a site like this helps me alot, ask away it really does help as you will get lots of suggestions and feedback which will help you and show you that you are not alone. :)

softie profile image
softie

Hi, it is a hard thing to deal with and people don't take me seriously just because I seem to look " ok ", life is a struggle, the tiredness, pains and aches etc which none of my family seem to grasp... the worst bit I think is the memory relapses I get and sometimes I cannot get words out properly which can be embarrassing...I have no outside friends and no family come to see me, feel like i'm "swept under the carpet " I need a friend too.

rafael profile image
rafael

Hi there

I have only just realised that my memory loss is due to the Lupus and not getting old. My memory is that bad when I write a list of my medications before taking them, by the time I write my last medication on the list I have already forgotten what I have taken!

I am on Azathiprine and suffering from muscle pain and also joint pain.

Would like to keep in touch.

Take care

Rafael

You may also like...

New and Unsure about me

am new here and was wondering about symptoms of Lupus. My doctor is sending me to a rheumatologist...

I'm new to this, wondering if this is flare

biopsy.. So maybe this tipped it? My anxiety has been climbing and the non medical stuff is losing...

Looking for new lupies for mutual support and understanding!

I've had Lupus for 12 years, I was diagnosed when I was 11 and was in the last stage of kidney...