List of the most popular hashtags for theme #RHEUMATOIDARTHRITISWARRIOR

. . . . .. . . . . . . . . . . . . #shoutout #invisibleillness #lupus #lupusawareness #lupuswarrior #lupusproblems #yougotthis #sjogrenssyndrome #sjogrens #raynaudsdisease #raynauds #sle #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #warrior #fighter #hughessyndrome #autoimmunedisease #autoimmunewarrior

So she rested and tried again tomorrow. #chronicillness #rheumatoidarthritiswarrior #rheumatoiddisease #autoimmunedisease #spoonie #rheumatoidarthritis #lupus #fibromyalgia #chronicpain

That chronic illness glow up #autoimmunedisease #rheumatoidarthritiswarrior #rheumatoidarthritis #chronicfatiguesyndrome #chronicpain #chronicillness #fibromyalgia

: Sleeping is like the refresh button. Sometimes it works and other times it doesn’t - as if the internet connection is down. We always hope that when we go to sleep (if we do) that we will feel better in the morning, even if it’s just a little bit. Comment below if you feel like sleep sometimes helps you feel a bit better in the morning. Follow @how.u.feeling for more!

: It’s okay to be emotional. I don’t understand why people think that it’s only okay for everyone to be happy and joyful all of the time. It’s okay to be sad because sometimes after battling an illness for so long and suffering everyday, sadness is just what you feel. You are frustrated, fatigued and sometimes hopeless for a better future. However the key is to not let these emotions control the quality of your life. Take a day every week to be sad and frustrated. Scream at the top of your lungs and cry your hearts out. But after that, start to reshape your thoughts. Try to be grateful for all that you have - that could be that you have food on the table or that you have access to medical care because not everyone does. We control how we want to live our lives. There are barriers that limit our abilities but it’s our mind that pushes us past them. Type YES if you agree. Follow @how.u.feeling for more!

: Always be kind because you never know what people are dealing with behind closed doors. Comment below if you agree. Follow @how.u.feeling for more!

LOUD AND PROUD, YA’LL // as some of you guys know, in real life I’m @laura_macleod and I post about my illness over there too, even though it’s really my “personal” page. And what could be more personal than this all consuming illness that hasn’t left me alone or left my mind for the last 4 years... right? well, a few weeks ago my boyfriend suggested that I try to be more upbeat over there, that my fundraising might go better if I put on a smile. I totally understand where he’s coming from, but the thing is, I think it’s IMPORTANT for people to know how bad it truly is. That this Lyme Disease thing is ruining lives and that the majority of them (my followers) live in CT (I grew up there), which is famous for its #lyme. And so I speak out, to spread awareness, to help people understand, as an outlet for myself and as a way to get #GoFundMe donations - because I need them to keep living. Have you guys ever dealt with this type of criticism or suggestion? I’m curious what your thoughts are...

: We all need to listen to our bodies and if we need rest then we have to take it. You are not wasting your day by staying inside but rather you are taking care of yourself. We did this yesterday and our bodies thank us for it. Remember, life is all about balance. Follow @how.u.feeling for more!

- as I limp out of his office #chronicpain #chronicillness #rheumatoidarthritis #rheumatoidarthritiswarrior #autoimmunedisease #fibromyalgia #lupus #lymedisease