Why am I not able to remember what things are, th... - LUPUS UK

LUPUS UK

32,249 members28,608 posts

Why am I not able to remember what things are, the names of them, and when I talk to someone, I can't think of the right words, stomach pain

Alfie1974 profile image
4 Replies

So much stomach pain, and the joint pain and, I can just go on and on, so much I am going through and I have no dr or insurance, and I just want a friend who's going through the same things, and a lot of it I do not know about or understand, please contact me back, and I thank you from the bottom of my heart...Alfie

Written by
Alfie1974 profile image
Alfie1974
To view profiles and participate in discussions please or .
4 Replies
dgleds profile image
dgleds

I get stomach issues from my medication plaquinil that I take for lupus..also if I take non steroid anti inflammatories..even if I take with milk or food..

My brain is kinda fuzzy from I guess lupus...

joint pain come and goes for me...

my hearts been doing twinges, so im getting an ecg on Monday..and more blood tests...

so u have no doctor? I dont have a steady doctor...

SarahHeney profile image
SarahHeney

Are you on Facebook Alfie? Lupus UK have a page with over 5000 members which is well run and more of a chat forum. Or if you are in America they slso have similar groups on Facebook. Just s thought as it sounds like you vould do with some friends with lupus.x

daisyd profile image
daisyd

Morning sorry about how poorly you feel as I have mentioned in other posts, please see the Healthunlocked site on Hughes syndrome, regarding memory problems

Carcrashgal profile image
Carcrashgal

'Use a noun!' is my husband's most common phrase these days - he knows I just can't remember words sometimes (and me a writer and publisher!) and it's *so* frustrating for both of us. Alfie, sounds like you need someone to talk to who's going to understand this hateful disease - this forum's great at that too as we're all going through variants of the same thing. But it also sounds like you definitely need a medic - where are you? And you might find books like Talking About Lupus by Triona Holden useful. GrandmaCarol's right too: rest up, and don't try to do too much. It sounds trite, but there will be good days and I think we all live for them! Hang on in there. Jo

Not what you're looking for?

You may also like...

The irony of needing to remember so many important things when you can't remember What they were

Box after box of tablets and lotions and potions. So many appointments my calender is full, parents...

What can I do more of to not feel loanley and in pain

I don't go out much. I don't mix good with people. I can hardly walk . I vidio chat to famlie some...
nita57 profile image

Why I toot the benefits of meditation, exercise and diet and why I think it might help to reduce autoimmune inflammation

Those of you who know me here know I often, probably too often, toot the benefits of my anxiety...
Roarah profile image

No support

Not sure if this is a normal feeling to have or not but I feel like I have no support with my pain...

Almost feel like im killing myself with the fatigue

Hi their I have had lupus since 2012 June time am now 20 and seem to be struggling slightly as time...
Danielle2419 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.