new to Lupus if that's what it is... love to shar... - LUPUS UK

LUPUS UK

32,248 members28,608 posts

new to Lupus if that's what it is... love to share with anyone local,

Nickle profile image
5 Replies

Hi, I’m new to Lupus and all that goes with it, I’ve been on the roller coaster of diagnosis for the past year and they still haven't decided, but they have decided enough for me to trial hydroxy' and I started 2 months ago, I think I might be feeling better but not sure, I’ll give it another few months, but had a tough year with spontaneous idiopathic urticaria, which the allergist didn’t think was linked, but I and my rheumy did !!! Medical professionals eh!! it took them 5 months to get it under control, with me having sever reactions about 2-3 times a week, which was draining, but now I’ve gone through all the meds the last in a long line worked.

I love to meet or chat with anyone local, as I find email and blogs useful but nothing beats face to face, please message me or reply if anyone is local.

Hope you all have a happy Christmas

opps sorry guys local is gloucestershire - between gloucester and cheltenham in Churchdown ...

Written by
Nickle profile image
Nickle
To view profiles and participate in discussions please or .
5 Replies

Hey Nickie,,i hope you are doing ok? Hydroxy/plaquenil,,i have used for 4months now and i have improved skin.Hey,we have a group on facebook.Look us up,,,Lupus is real !! xx

Helsbels profile image
Helsbels

Hello

I have had lupus for a long time and can offer you some help if you need it. Also, you don't say where 'local' is!!

Merry Christmas

x

janiceray profile image
janiceray

If you let us know where you live we maybe able to help,

Or contact Lupus U/K not only can they supply you with info they will be able to tell you who to contact,there are groups in most area's

Happy Christmasx

Nickle profile image
Nickle

thanks for your comments ...

opps sorry guys local is gloucestershire - between gloucester and cheltenham in Churchdown ...

Paul_Howard profile image
Paul_HowardPartnerLUPUS UK

Hi Nickle,

Perhaps you'd like to get in touch with the Western lupus group? I'm now going to send you a message with the group contact details.

Not what you're looking for?

You may also like...

New to Lupus.... possibly!

Hi, my diagnosis was ANA positive without any clinical features of SLE. However I saw the...
Scubes profile image

New to Lupus

Hi This is the first time iv posted about lupus. I was diagnosed with Sjogrens about 6 years ago...
AnnieKhan profile image

New to lupus..

Hi everyone, I was diagnosed with lupus just before christmas following a biopsy. I am new to this...

Is it Lupus?

hello all good to meet you here. I am in the process after many years of battling inflammatory...
GottaAsk profile image

Is it lupus

Hi I am just wondering if anybody could give me some advice please. I have been ill since 2006, I...
heather26 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.