When you are in a flare can it feel like you have the flu? I think I may have had my first "flare" past 2 weeks ive had a pressure like headache and today now I just feel like a have the flu (achiness, tired) but I don't have the flu... and if this is a 'flare' do I call the rheumo or just wait it out? what is a True FLARE? ? ? im really new to this so sorry if this sounds stupid
I have asked the same question, i also have fibro so it gets confusing what is what. but, i do feel like i have the flu, achy all over, ect. ect. just like the flu, i guess you would consider that a flare, problem is i can be like that for months - from talking to people here i think everybody is different. i think the flares come and go
Hi Potslupus
Your question isn't stupid, and we've all asked this one time or another. When you have an increase in symptoms like you're describing, I would say you're in a flare. Try to rest even more, and if you feel your symptoms worsening, then call your doctor - whoever you have more confidence in. For me, I can get in to see my GP quicker than my rheumie. If your symptoms are extreme - then you'd head to the ER. I've experienced the pressure headache you described last few weeks, and I had a flare last week and I ended up in bed rest.
I hope you're feeling better : )
do the more flares you have closer together mean the worse you are ? :/ how do you know if you have organ involvement ... because I felt like this about 2 months ago too.... I just don't know when to call the doctor
Yep, it can definitely feel that way. That's how I know I'm in a flare.
As for organ involvement... if you have anything unusual or new, I would call the doctor. For example, chest pain, problems with urinating or changes in your urine characteristics (ex. blood in urine), abnormal bruising, swollen lymph nodes, etc. I would also keep track of your flares in a journal or calendar so that next time you visit the doctor, s/he can see how often you flare, and what might trigger them and what they consist of (like the flu feeling).
Hello Potslupus! My flares feel exactly the same way. For me lots and lots of rest will turn it around quicker than anything but looking back I think it was a learning experience to figure that out. When you’re new to lupus there’s so much to learn! Because lupus is unique for everyone it’ll just take time to learn what your triggers are, how to prevent them when you can and how to deal with them when you can’t. Always, listen to your gut instinct and when in doubt call your dr! Especially for new or worsening symptoms. Hope you feel better soon!!
Renee