#lupussle

[lightscamerasmashem]

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A post shared by Anna Walden (@theonlyebunny)

#Mood What can I say, other than I don't give up easily...... #Friday #Life #LifeWithLupus #IWontStop #Oklahoma #Spoonie #LupusSLE #DiscpidLupus #SjogrenSyndrome #Vasculitis #RA #Arthritis #AdiesTonicPupil #Fibro #OneOfThoseDays #VideoOfTheDay #VideoOfInstagram #LaidUp #StuckInBed #LupusFlare #LupusWarrior (at Claremore Lake) https://www.instagram.com/p/B0HQo8qjcy6/?igshid=ozoo1cfs5w3e

[beautifulrosebutterfly-blog]

Prednisone

I got put back on it been awhile since I was on it

[kirasunshine]

#everythinghurtsandimdying But really, Everything hurts and I’m dying. #lupusawareness #lupus #lupussle #sjogrens #fibromyalgia #fibro #chronicillness #chronicpain #chronicillnessadvocate https://www.instagram.com/p/BncCc6AACRr/?utm_source=ig_tumblr_share&igshid=wdteo3f9rq2f

[ambizness-blog]

Fuck Lupus #ButterflyRash #lupus #sle #lupussle https://www.instagram.com/p/Bt97x0NHOF1/?utm_source=ig_tumblr_share&igshid=5nu3mn4tnkrp

[lindgrenjulie]

Minus chronic headaches, chest pain and Anxiety and depression… freaking wonder I’m still standing vertical #lupus #lupusawareness #sle #lupussle #kidneytransplant @selenagomez #ahousewifecom https://www.instagram.com/p/CY2H9kiN70J/?utm_medium=tumblr

[kirasunshine]

This is so important. I’ve been sick since I was 18 and today I am 26. I have had 33 hospital stays. That’s an average of four times a year. As I’m writing this I’m contemplating letting my husband take me to the ER for day five of pain. Just because I’m young doesn’t mean I’m not in the same pain of a 65 year old woman.

[Image Description: An orange color block with text that reads “support young people with chronic pain”]

Support people in their teens, 20s, and 30s who deal with chronic pain and are constantly dismissed by being told that they’re “too young” to know what pain is.

Your experiences are real, the pain you go through is real, and you deserve support and care as much as anyone else.

[thrivingcheermom-blog]

It’s up to you to see the beauty in every day things.... 💜VICTORY💜 #saved #victory #moderndayruth #weekendvibes #saturday #lupusSLE #warrior #purposedriven #voiceofhope #faith

[diorhealth2wellbeing-blog]

I have put up some useful information regarding Lupus and fibromyalgia i myself have family and friends with these two conditions. #lupus #lupuswarrior #lupussucks #lupuswalk #lupusflare #lupusrash #ihavelupus #lupusfighter #lupussle #fightinglupus #lupusawareness #kickinglupusbutt #fibromyalgia #fibromyalgiasucks #fibromyalgiawarrior #fightingfibromyalgia #fibromyalgiaawareness #fibromyalgiafighter #diorhealth2wellbeing #dh2w #diorh2w #lupusandfibromyalgia #lupusfibromyalgia

[50-shadesof-sexy]

This is what Anna had to say about Lupus and LimeLight. 💜 This is the Lupus, and I am so thankful for my LimeLight. As time goes an all natural/chemical free skincare continues to sooth, heal, & repair years of damaged caused by medications and the several autoimmune diseases I continue to battle. The coverage from our Makeup obviously makes me happy, last all day, is affordable, but most importantly gives me normalcy. Normalcy is lacking in ones life of fighting these diseases.............. I can use these products knowing, they will not further any damage to my ridiculously delicate skin. I am comfortable in my own skin either way, but it is nice to be able to blend in, without gazing eyes from every direction, when I choose to do so. ♡♡♡ #LupusCanKissIt #HyperPigmentation #ButterflyRash #LupusSLE #DiscoidLupus #SjogrensSyndrome #RA #Vadculitis #limelightbyalcone #chemicalfreeskincare #askmetoday #flawlessmakeup #flawlessskin #bestskincareever

[paddypatt-blog]

There are no medical claims here, just random people that have had an amazing experience changing their lives nutritionally. Please share and spread the love. 😊😊 My name is Deveen and this my own testimony. I was introduced to MOA in November 2016 by my Cousin Jude. She knew i have Lupus SLE and Nephritis which affects the kidneys i also have a fractured hip so am in constant pain with it. She knew how it affects my health and day to day life. She told me when she heard about MOA she instantly thought of me. She asked me to try a bottle and i have ever since. Since taking it i have had loads of energy and my pain has reduced. I went to see my renal consultant last month. He looked at my kidney function results and turn to me and said my kidney function have returned to normal. I have not had a normal fuctioning kidney since to 2007. He asked me what i have done diffrent i said MOA. I was shocked happy overwhelmed with joy. It's since taking MOA it's improved. The only thing I've done different is take MOA. No more chemotherapy for me. I believed in this product so much that i have now joined the team to share my experience and tell others about this amazing superfood drink. It really is the Mother Of All. #MOA #healthy #nutrition #nomorechemo #happy #renal #superfoods #kidneyfunction #nephritis #lupussle #lupus #change #pain #testomony #family #love

[lightscamerasmashem]

I didn't step out of bed until 2 or 3 PM-ish, & ALL the #FurrBabies cuddled with me. They just KNOW, when thing's aren't right. These were the only 2, not tucked completely understand the blankets. #LupusProblems #SpringIsHere #FlaringHard #LupusFlare #AutoImmune #SpringIsAHardTransition #LupusSLE #DiscpidLupus #SjogrenSyndrome #Vasculitis #RA #Arthritis #AdiesTonicPupil #Fibro #Spoonie #LupusWarrior #CuddleBuddy #Puppy #Chihuahua #CatsOfInstagram #Calico https://www.instagram.com/p/Bv0dJAjHwLw/?utm_source=ig_tumblr_share&igshid=1rgbjk6ixeq9m

[beautifulrosebutterfly-blog]

[kirasunshine]

Hello and I’m back!

Let me catch you up to date.

My name is Kira. I’m a 26 year old girl from Cleveland, OH-IO! I have Lupus SLE, Sjogrens, Fibromyalgia, POTS, IC, Joint Hypermobility Syndrome, Narcolepsy, Epilepsy, Cataplexy and I’m sure in there I am forgetting something, too many to remember.

I am married to an amazing man named Randy. He unfortunately is my caretaker. We have been together for four years August 16. Although I am disabled I am able to fold clothes, do a few dishes, give myself a bath sometimes, and little task. I can’t do large task like carrying laundry up the stairs, scrubbing bathrooms, doing too many dishes, make an extravagant dinner for Randy when he comes home from work. 

My mother and uncle are my other caretakers. No doctors appointments alone, never left alone. I can not function on my own and rely on the help of others. In the last few years my lupus has become so strong I had to drop out of college, and I am no longer able to work. I spend most of my days sitting in the house.

I went into a coma in April 2017 and ruined my lungs so when its hot I cant be outside.

Hope you follow along with my journey.

-Sickgirlproblems

[lindgrenjulie]

Just got this from @cultbeauty @supergoop #sunscreen good for people with #lupus #sle #lupussle #yay #awesome #beautyblogger #ahousewifebeauty #beauty #skincare #beautyhaul #ilovebeauty #ilovebeautydk #ahousewifecom # NoPaidPartnership #NoPayedContent #NoDiscount #AllBoughtContent #influencer https://www.instagram.com/p/CHU3FHVDpmQ/?igshid=162qr2b8rf4x7

[rhematologistclinicpune]

Meet the best Rheumatologist in Pune? Dr.Nilesh Patil is a well known Specialist Doctor for Rheumatologist.He provides the Lupus/sle Treatment in Pune.

[jesseniasnipes]

I’ve been waiting for three days for my doc -er- nurse practitioner to call me back about my lab results. She called me last Friday but the phone connection wasn’t clear so she just hangs up instead of calling back. GREAT! I had to wait all weekend long for lab results. Called first thing Monday morning and I’m still waiting for a call back. For someone who was so insistent that I had HIV because of a chronic recurrence of mouth thrush, she’s not in a hurry to reveal the results to me. This is the third nurse practitioner that I have seen at my doctor’s office that doesn’t have great bedside manners. Not only that, my liver enzymes are coming back pretty high so I’m literally biting my nails to what could be wrong or go wrong. My wonderful GI doc told me that since everything with my stomach was fine it could have something to do with my bones. I trust him more than I trust this *new* NP. Anyway back to the whole HIV shebang. I explain to this NP that I’m tested yearly for HIV (did one at my most recent OBGYN exam) but she was adamant that I could’ve been around someone with HIV. Uh, no. Let’s not play this game and I knew where she was going with the whole, “being around HIV” comment seeing as I’m an AA female #ChronicallyIllWhileBeingBlack Just pissed me all the way off. Plus I’m having to deal with idiots in my personal life so this doesn’t make it any better. Maybe I should go back to sleep, LOL.