Summer is coming! LUPUS FRIENDS We DON’T get prot... - LUPUS UK

LUPUS UK

31,845 members28,189 posts

Summer is coming! LUPUS FRIENDS We DON’T get protected from our God of Sun 🌞 DON’T expose yourself too much outside.

Mei4u2c profile image
0 Replies

Hi everyone! This is Mei. I have joined the group since 2015. I haven’t been updated anything much because I’m still battling with my complications Lupus for 22 years. I recently have loss a lot of hair, (this is ONLY from one wash) I feel so depressed each time I go get my hair washed. I asked my family please let me shaved but they all said NO. Heart, Lungs and Kidneys are the most common for Lupus to attack. Now I have fluids in both of my lungs. (left side has collapsed too much water) I can’t even take deep breath, it hurts when I breathe, It hurts can’t sneezed 🤧, I can’t cough…my chest hurt, you all can imagine how that was and new syncope episodes (fainted with no sign) I hit my head on the bathtub, I blacked out in the kitchen while washing dishes, I fell backwards and I have nothing to hold from my back, so my butt went down first then my head on the floor. I crawled up to my room to call my husband my head was bleeding and my butt was hurting so bad. He took me to Emergency. Finally I got 2 stitches on my left head and fractured my tailbone S4. This happened 2 months ago I just got everything healed pretty good. 4 days ago OOPS I DID IT AGAIN😩 this time in the opposite side. OMG 😳. No one knows why I kept fainting (syncope). I quit my job there’s no way I can handle too much trouble for myself. Lupus is scary but you manage it well you can live on like other people. Get more rest and we need to have enough sleep at least 8-15 hrs for me only some time I can sleep up to 3 days just got up find some things to eat and take my med back to sleep get up and pee lol no energy at all … and you’ll never known what comes next. I HOPE ALL MY LUPUS FRIENDS ARE DOING WELL AND GETTING BETTER EVERY DAY 🥰

Written by
Mei4u2c profile image
Mei4u2c
To view profiles and participate in discussions please or .
Read more about...

You may also like...

Seizures and Lupus related?

ago with lupus, but I can’t figure out if these episodes I’ve been having are related to lupus....

Anyone get nerve pain?

muscles. Can nerve's inflame too with lupus? I get these pains in my neck and shoulders, my head...

Chest pain, palpitations & confusion. Help!

wake me up at night and I have to sleep in a certain position to breath. I've been to A&E so many...

Can anybody relate? How long did it take to be diagnosed?

wrist was in a bandage because it started hurting. I mainly get the pain on the right side of my...

Does lupus get worse?

Hi all hope your well. Just a quick one can lupus get worse over time? I have been diagnosed 2yrs...