Lupus sufferers : Hullo everyone, Iam in my fifty’s... - LUPUS UK

LUPUS UK

32,212 members28,556 posts

Lupus sufferers

Oval profile image
Oval
5 Replies

Hullo everyone,

Iam in my fifty’s and have been diagnosed with Lupus just last month! Have been living a healthy and happy life until I started experiencing constant pains in my right leg! Iam happy to share and hear from people suffering from the same illness!

Written by
Oval profile image
Oval
To view profiles and participate in discussions please or .
Read more about...
5 Replies
Ceri-NorthWales profile image
Ceri-NorthWales

Gosh, Oval, I'm so sorry for your recent diagnosis. It is a huge shock. Pleaase take all the time you need to process and deal with it. It is so difficult!

Unfortunately, I can't help much as I'm also recenly diagnosed and been going through a tough time trrying to get healthcare. What I can say though, is how much of a llifesaver this forum is! I have had so much help and support from so many here and this has helped me get the right treatment for long standing, untreated B12 deficiency.

There is a whole wealth on knowledge on this forum. Please never be afriad to ask - no matter how big or small.

Welcome to the forum and I wish you well with your diagnosis x

Forgot2mention profile image
Forgot2mention in reply toCeri-NorthWales

Hi ceri, sounds like you are feeling a bit more positive, glad to hear it

Lupiknits profile image
Lupiknits

Welcome! I cling to this forum although I have an assortment of auto immune disorders.

It’s a good place to be, for support, advice, sharing, joking, venting. Always someone here

Redfox25 profile image
Redfox25

Welcome Oval. I had a diagnosis of glandular fever which was all fine until I got pain in my right hip and I thought, 'this isn't right for glandular fever'. And that was the beginning of me figuring out for myself that I had lupus. It's still very hard to take now that I have an official diagnosis and I was in denial for a bit.

This forum is great, so you've landed in the right place. Some advice I have received is to learn as much about lupus as you can. There is a lot of really useful information on the Lupus UK website. The Lupus Encyclopedia is a very very informative handbook with tonnes of practical advice. It's about £25 but worth it.

Forgot2mention profile image
Forgot2mention

Hi, oval welcome to this site. I joined in january as it is my granddaughter that has lupus, it affected her brain but thankfully she is now recovering. You will find on here that you can talk to people with same issues as you, or you could just have a good old rant there’s always someone to listen. Sorry about your diagnosis and hope you get help soon 😘

Not what you're looking for?

You may also like...

Lupus nephritis and pregnancy

. Can any one pls tell me whether I can get pregnant after remission... And is there any one who...

losing weight

just backfrom the doc and i have lost eight pounds in 2 weeks iam so happy he said the more i lose...
scottty profile image

Dear all lupus sufferers

Can you close your fingers to palm/ fist in the morning??. Im query lupus now from original...
summer32 profile image

whom suffers chest and lung pain, is it fybriomialga or lupus....

does anyone whom also suffers from fybriomialga experience sever pain in there chest and also there...
mojo profile image

parents with children who have lupus

hi im just wandering if there are any parents who have children or loved with lupus as my daughter...
kathy43 profile image

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.