Can Blog
Yes we Can

Home Page




Posts Tagged ‘Lupus’

What does it mean when blood work shows you have connective tissue?

I know one possibility is lupus, is there others?

By: ~♥~ *CHEEKY* ~♥~



6 Comments

Tired of waking up tired. Anyone have lupus?

I am so tired of waking up and not be able to actually wake up! It makes it difficult to function through out the day and I feel like I’m in a brain fog that won’t let up.
Does anyone else with lupus encounter this?

By: MsElainious



1 Comment

does someone with lupus have children?

my frend have lupus. she want very much to have a baby but she is scared for his life to do that.e pregnancy for her must be fatal

By: cojocaru s



No Comments

Does anyone here have Lupus SLE?

im 21, and was just diagnosed with lupus a few months ago. im struggling to find a way to continue school and just life in general. I get tired alot and my legs hurt randomly..sometimes so much I cant even walk right. Anyone else has experience with lupus and can offer me some advice? Does this get better…how many times has it been active and how do u know if ur in remission? i think im in remission, but im so scared that ill go back to school and then itll be active again and ill have to quit again.

how do u guys deal with this back and forth thing? how do u ever get anything done?

By: jeannes85



No Comments

lupus and cant work?

hi my aunt has being diagnosed with lupus. she is so sick she’s been out of work. what benefits will she be able to claim can anyone please tell me . thanks
will all her symptoms go with the meds ? shes so tired and aches and breathless too

By: Lisa N



No Comments

what exactly is lupus?

i found out one of my cousins died.. all i know is that she had lupus. i have no idea what that is..

By: nottrina



No Comments

Does Crohn’s disease have these symptoms? Also, does Crohn’s disease occur with Lupus?

Bloating after eating (or even drinking cool/cold water)
Stiff joints
Bloody, mucousy, floating stools. (WITHOUT any pain when passing).

Is their an association between Lupus and Crohn’s disease?

By: MaluLanix0x



1 Comment

could someone explain there lupus symptoms?

could someone with lupus please explain what symptoms started first and how they have progressed. thanks

By: Aspen13



No Comments

newly diagnosed w/ lupus, any tips on coping?

I have SLE. I’m having lots of nausea,vomiting, abdominal pain, and headaches.

By: Rachel S



10 Comments

I’m on oxycontin. I have Lupus and Fibromyalgia. I’m still in horrid pain?

I was diagnosed with Lupus(SLE) this year and Fibromyalgia a few years ago, but believe it all started after a bout of very serious(hospitalized because of spleen and liver) mono when I was 17yrs old. I have been on percocet 10/325 every 4-6 hour max 4 day for the last 4 YEARS.. recently it got switched to 20 mg of oxycontin twice a day with oxycontin IR 5mg also twice a day… problem is it’s still not working and I’m sitting here typing with tears running down my cheeks… I put a call into my doctor..no call back yet… It’s full body agony.. I can’t take this anymore…I don’t know how to tell my doc I need more meds or different, or something… I have tried yoga, nerve blocks, operations, therapy, etc… in the past few years… nothing works, I have three children who need me and all I want to do is curl up in a ball and die… I don’t know what to do anymore… Can anyone advise?
I was on prednisone for 11 yrs.. as a result I have osteopenia( swiss cheese for bones)
I just got a call from the nurse, not the nice one, even though the dr. said to call if it didn’t work so he could adjust the dose, she says he said he’s not changing anything and to call my rhematologist( who doesn’t want to be responsible for pain management) if that’s not ok with me…
Plus I did go to a pain clinic for 3 yrs, after many different treatments, nerve blocks, operations etc…, they tried to get new equipment for their office by saying I needed to have a certain operation( that I found out I didn’t need from 2 dr.s) so I stopped going there.. Primary doc( the one I tried calling) tried to get me into 3 separate pain clinics.. all have said they can’t do anything for my condition except meds, too advanced in disease too help, so they won’t take me. That’s why I get meds from primary now… and now no help is coming, who knows if she even talked to him..probably not

By: Desiree



5 Comments