#lupusflare

[izyjean]

I was able to do a small amount of yoga tonight & that’s helped immensely with my mood of not finishing my routine. I’ve also been reading an amazing book, by Beth Evans, of where she talks about her OCD & how it’s shaped her routines & I don’t feel so alone in having to do certain things to feel successful in my day. I still don’t know what’s in the air, but I have prayed about my frustration & cut ties with many people today. Idk why it can’t be a mutual respect & understanding that we may see things differently, & that’s okay, but I don’t have time nor care to want that drama in my life. I’m not sorry for wanting peace & respect. I am still extremely shaky, not keeping food down & relying on my neuropathy oils, vitamins & ibuprofen for the pain, I just really wish one symptom would subside so I could manage the others. I work a double tomorrow & back to my other job starting Sunday evening. I’m absolutely exhausted & it’s unreal that it takes this much to live comfortably, but nevertheless, not surprised. I hope everyone continues to be open-minded, loving & kind to everyone, everywhere- you don’t know what’s going on behind closed doors, so just let it be. Happy evening. 💛 #momvlog #lupuswarrior #dailycheerup #yoga #fitness #thriver #lifestyle #lupusflare #nottodaysatan #booklover #clouds #photography #chronicillness #autoimmunedisease https://www.instagram.com/p/CqWyNmXMtTP/?igshid=NGJjMDIxMWI=

#momvlog #lupuswarrior #dailycheerup #yoga #fitness #thriver #lifestyle #lupusflare #nottodaysatan #booklover #clouds #photography #chronicillness #autoimmunedisease

[geektalkus]

Had insomnia for hours. Thanks lupus. Or maybe sensory overload. I would say the latter. One day I can fall a sleep in a middle of a sentence next I can’t sleep for 36 hours. I’ve taken my normal bedtime medication plus 5x 10mg melatonins & 2 of my muscles relaxer that’s supposed to help with pain & sleep. This is life. Unscripted. It just gets old being this way. #lupus #lupussucks #lupusflare https://www.instagram.com/p/CmGpi-TO_xR/?igshid=NGJjMDIxMWI=

#lupus #lupussucks #lupusflare

[lupushope]

For Swollen Limbs, which is super common for people diagnosed with lupus, lymphatic drainage is essential, as it is responsible for removing all body waste. Many days, I can see my face all puffed up without reason – that’s a call out for Abhyanga time! Do you want to know how to Perform an Abhyanga self-massage at home? With my kids at school and leaving home early, it’s hard to start my day with Abhyanga. I like to do my daily self-massage at night before going to bed because that’s when my day is calmer. That’s when I can pay more attention to myself and what works best for my schedule; I suggest you do the same. In my latest blog I am a sharing all the tips and basic oils for this amazing therapeutic habit that you can do yourself and at home. No excuses. We know that not loving ourselves is a recipe to pain and failure. Our bodies and mind are fully connected and we need to pay attention to both. Check my blog at www.LupusHope.org to learn more. #abhyanga #banyanbotanicals #banyanoil @banyanbotanicals #ayurveda #ayurvedalifestyle #ayurvedic #ayurvedicmedicine #autoimmunedisease #lupus #lupusawareness #lupuswarrior #lupusflare #lupusfighter #pain #inflammation #inflammationrelief (at Portland, Oregon) https://www.instagram.com/p/CjByTMLv78G/?igshid=NGJjMDIxMWI=

#abhyanga #banyanbotanicals #banyanoil #ayurveda #ayurvedalifestyle #ayurvedic #ayurvedicmedicine #autoimmunedisease #lupus #lupusawareness #lupuswarrior #lupusflare #lupusfighter #pain #inflammation #inflammationrelief

[heatherjpp13]

Do I complain? NO! Do I ever tell you when I feel my worse? NO! I love my life & I live it to the best I can. My son is the reason I fight daily. My other prognosis' are just that. So I bleed...& I know because sometimes it won't stop...Anemia...I have COPD & Asthma, I have Kidney issues, yet I push through with my brain having issues from Lupus. I don't give up & I fucking live my life. I try to record daily because it's all I have for Tristan to remember. Life is short...love, live, & enjoy💜💜💜💜💜💜my cousin died from this disease & I miss her every fucking day!!! #lupuswarrior #lupusawareness #loinpainhematuriasyndromeawarenessday #sickpost #lupus #sle #lupusfighter #lupussucks #lupusflare #lupusawarenessmonth #lupuslife #lupusadvocate #lupusstrong #edsawareness #lupusproblems #lupussurvivor #ankylosingspondylitis #lupussupport #chronicillnessmemes #lupuswarriors #knowlupus #rheumatoidarthritis #lupusfoundation #crps #lupusfacts #chronsdisease #lupie #lupusnephritis #gastroparesis #fibrowarrior https://www.instagram.com/p/CfmuoJuFwVR/?igshid=NGJjMDIxMWI=

#lupuswarrior #lupusawareness #loinpainhematuriasyndromeawarenessday #sickpost #lupus #sle #lupusfighter #lupussucks #lupusflare #lupusawarenessmonth #lupuslife #lupusadvocate #lupusstrong #edsawareness #lupusproblems #lupussurvivor #ankylosingspondylitis #lupussupport #chronicillnessmemes #lupuswarriors #knowlupus #rheumatoidarthritis #lupusfoundation #crps #lupusfacts #chronsdisease #lupie #lupusnephritis #gastroparesis #fibrowarrior

[spooniestrong]

Things To Avoid If You Have Lupus

#spooniestrong #spoonie #lupus #sle #systemic lupus erythematosus #flare

[nagisama]

I have lupus and my hands are shaking so bad I feel like I’m about to die. Any advice would be rad!!

#lupussucks #lupusproblems #lupusflare

[stormielikeweather]

Chronic illness does not mean life is over. It is not a marker on the grave. It is something challenging.

Not something to overcome but something to adjust to. Something that life hereafter will include. It starts not with diagnosis, but with symptoms. Once diagnosed there is hope. There is community. There are good days again with time, with the medication combination catered to individual needs there is life again.

It is true that nothing will ever be the same again, but such is life. Every day will be different than the last with or without a chronic illness.

Some days will be hard, but not all of them.

Rest when needed. Don’t give up if a medication fails. Advocate. Do not feel guilty because of illness. Keep dreaming. Keep accomplishing goals.

Do not be afraid of flares. They will come and go. Life is there for your taking of it. Hold on to it. Relish in it.

#chronic illness #rheumatoid disease #rheumatoidarthritis #lupusflare #auto immune disease #motivation #positive vibes #positivity

[burnedouthippie]

Finally got accepted as a new patient with a rheumatologist after months and months of waiting 🙌🏻🙌🏻 pray the treatment process treats me well yall.

#lupussucks #lupusflare #life with lupus #lupusawareness #lupusproblems #me #personal #loopy babes unite

[shades0fblu3]

Shout out to all the people in chronic pain, who decide to keep it to themselves, who think that complaining about it will only disturb others, to all the people who act like they're fine around healthy people. Shout out to all the people that are in pain right now. You are seen, you are applauded.

#chronic pain #chronic disease #life with lupus #lupusawareness #lupusflare

[alexsis]

Do you ever feel like u can’t get out of bed like ur tethered in a way. And not in a way in which u want to be but in a way that feels constricting? But there’s nothing u can do about it? The pain is worse today than normal days. Some days it makes me question how much longer will this go on? How long can I live like this?

#mswarrior #msfighter #lupus #systemic lupus erythematosus #lupuswarrior #lupusflare #chemosucks #ivig #momlife #drowing

[chronically-moody]

Hi! My sister was just diagnosed with lupus today. What can i do to help her??

Hi there,

First I want to say that I am very sorry to hear that. Lupus is a hard disease for both those living with it, and their loved ones.

Lupus is different for everybody, but I would say the best thing you can do is to listen to her. She may be surrounded by a lot of people who do not believe she is sick, since lupus is largely an invisible illness. Make sure you're around to offer help, or to just tell her that you believe her and that you can't imagine how hard it is.

You and your sister will be in my thoughts and prayers

#lupus #lupustruth #chronic illness #spoonie #spoonie community #auto immune disease #lupusflare #disease

[geektalkus]

I wish the red in my face was from a filter but at last it’s from lupus. It’s from being “sick” for weeks on end. Not feeling like leaving the house or giving up weeks of my life for 1 good day. Not answering messages or phone calls because you know those people don’t understand what “sick” truly means. And when you try to explain to them they think you are just wanting attention or exaggerating about basically being bedridden with pain. This is my life with lupus. Unfiltered. Uncensored. Just me. #lupusflare #lupus #chronicillness #chronicpain https://www.instagram.com/p/CmBFNGgs0FX/?igshid=NGJjMDIxMWI=

#lupusflare #lupus #chronicillness #chronicpain

[thelupusdiariesofficial]

Pain

I hate the pain scales that they give you at the doctor’s office. The ones with all the little faces and you have to choose which one represent’s how much pain you are in. When you are in pain all the time you become numb to pain. I always say it is like being in a room and someone is either shouting or screaming, and the pain is always there. It is either shouting or screaming, but it is…

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#butyoudontlooksick #chronic pain #chronicdisease #chronicillness #chronicillnessawareness #chronicillnessblogger #chronicillnesscommunity #chronicillnessfighter #chronicillnessmeme #chronicillnessrecovery #chronicillnesswarrior #chronicpain #fibroflare #fibromyalgia #lupusawareness #lupusflare #pain

[creativetona]

Today is a good day.

Was able to get out of bed today, I even felt inspired to put together a look. Wide set pants from Old navy with a tucked in floral top and an oversized blazer. 

My hair is volumous to the Gods also so I feel great. I’m currently at the office and I love being here, specially when I’m blessed with days with little to no brain fog at times. thats where I take advantage and do as much as I can, because I know I dont get alot of clear days like this...

Less lupus pain=more things get done

but I have to be careful because if I go all in....I will pay for it for a couple of days.

So right now, we work, finish a realistic amount of work without over doing it. That is the plan for today, plus my outfit is poppin’.

#lupus #lupuswarrior #lupuscommunity #lupusconfessionals #fashionlover #chronic fatigue #chronic pain #dailyjournal #strongwomen #lupusflare #systematiclupus

[authenticallyjames]

For more information on Lupus, visit www.lupus.org and www.worldlupusday.org • #fightlupus #lupuswarrior #makelupusvisible #lupussupport #lupus #chronicillness #lupuswarrior #lupusawareness #autoimmunedisease #chronicpain #invisibleillness #sle #autoimmune #lupusfighter #lupussucks #lupusflare #rheumatoidarthritis #arthritis #lupuslife #lupusawarenessmonth #lupusproblems #butyoudontlooksick #chronicillnesswarrior #health (at Garfield Heights, Ohio) https://www.instagram.com/p/COtHnugrknu/?igshid=a9762d7ldasl

#fightlupus #lupuswarrior #makelupusvisible #lupussupport #lupus #chronicillness #lupusawareness #autoimmunedisease #chronicpain #invisibleillness #sle #autoimmune #lupusfighter #lupussucks #lupusflare #rheumatoidarthritis #arthritis #lupuslife #lupusawarenessmonth #lupusproblems #butyoudontlooksick #chronicillnesswarrior #health

[skjarsgaard]

Growth is important (especially in sweaters)

#knitblr #knitting #knitwear #yarn #yarnspirations #yarnart #lupuswarrior #lupusflare #lupustruth #sweater weather #handmade #knitterslife #knittersoftheworld #knitters of tumblr #knitstagram #knittersofig