Liste des hashtags les plus populaires par sujet #LUPUSWARRIORS

Shout out to everyone with #chronicillness #chronicpain and #chronicdisease who are fighting the battle that most people don’t understand and see their doctor more than their friends! Keep hanging in there! Do you use probiotic to help with your symptoms? Here's why you should consider to give it a try: probiotics are generally beneficial gut bacteria that a vital for development and support of your immune system. Particularly, they help to decrease flare up frequency and extend the #lupus and #autoimmunedisease remission length.⁣⠀ You can get more probiotics with your diet by consuming cultured and fermented foods such as yogurt with live cultures, kefir, acidophilus milk, miso, sauerkraut, and tempeh because they are naturally high in probiotics.⁣⠀ Another option is to take high quality probiotic supplements. ⁣⠀ I would like to let you know that everyone who would like to try out and experience the benefits can get FREE live potent probiotic (50 billion of good bacteria which is substantially more than in probiotic containing foods) and FREE high quality premium protein through my website. Both can be very helpful for people with Lupus and #autoimmunity. Protein can replenish nutrients that are often get depleted in people with lupus and #autoimmune disease , may help with energy and supporting recovery and healing process. Probiotic can help to improve digestion and absorption of nutrients and support the immune system. It’s truly free, no strings attached, worldwide shipping. You can get it through my website at https://lupusselfhelp.com/free or Just click the link in my instagram profile description @lupusselfhelp <<<===click

Getting w/ these kinds of comments on my @facebook page.. that people with #lupus can have long & fruitful lives! ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ can be manageable especially if diagnosed in a timely manner and appropriate treatment can be given. There are already about 160 rheumatologists in the country who can help you. There is #hopeforlupus. ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ (PS. I didn’t cover names anymore since they freely posted on my PUBLIC fb page, where I teach about rheum conditions in Filipino/Tagalog. These lupus warriors want the world to know they are living better w/ lupus, and they wish to inspire fellow chronic illness sufferers to never lose hope.) ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ #sle #chronicillness #rheum #rheumatology #PRA #testimony #patients #autoimmune #selenagomez #physician #womeninmedicine #lupuswarriors

Easing back into the selfies as my confidence comes back. I’m down to 15mg of prednisone and WOW, what a difference that has made. Not only is the moon face going down, my body feels better overall. I’m not as shaky and I feel somewhat in control of my body. Usually I react badly to weaning off the prednisone but I am trying to combat that this time around with lots of water, healthy nurtients, meditation, and exercise. I stretch daily, workout 2-3x a week, and I’ve been making sure I eat lots of veggies. I also have been taking turmeric and just added in probiotics. I’m not 100% but I’ve been feeling pretty dang good. How many of you have benefited from lifestyle changes? • • • #lupus #lupuswarriors #autoimmunedisease #invisibleillness #chronicillness #sjogrens #prednisone #health #wellness #healthy #feelinggood

How many of you deal with chronic fatigue? I just posted a new video discussing this topic. Fatigue is one of the top symptoms yet we rarely talk about how debilitating it can be. How do you all try to combat fatigue? You can find a link to the full video in my description box. • • • #lupus #lupuswarriors #lupuswarrior #autoimmunedisease #chronicfatigue #chronicillness #invisibleillness #fatigue #sjogrens

Not all illnesses are visible to everyone. When you are living with #lupus #autoimmunedisease #chronicpain or #chronicillness you may appear as a healthy looking person on the outside but be ill on the inside especially during your #invisibleillness flare ups and relapses. Some people judge you only by what they see on the outside because they don’t get to see what happens on the inside and how difficult it’s for you to fight with your symptoms every single day trying to feel and look good. The key is to find and surround yourself with people who get you and understand your challenges and raise #lupusawareness #chronicillnessawareness and #autoimmuneawareness P. S. I would like to let you know that FREE live potent probiotic and FREE high quality premium protein are now running out of stock and once free bottles are gone, they’re gone forever! Both can be very helpful for people with Lupus and #autoimmune conditions. Protein can replenish nutrients that are often get depleted in people with lupus and #autoimmune disease , may help with energy and supporting recovery and healing process. Probiotic can help to improve digestion and absorption of nutrients and strengthen the #immunesystem It’s truly free, no strings attached, worldwide shipping. But the are only a couple of days left to get it for FREE! Don’t delay and order yours today. You can get it through my website https://lupusselfhelp.com/free or Just click the link in my instagram profile description @lupusselfhelp <<<===click

#REALTALK// as everyone around me prepares to go out and get loose on a Friday night, I’m trying to be as confident as I can in my decision to (pretty much always) stay in. . . For a people pleaser that hasn’t quite been able to let go of caring about what people think of me, this is harder than it seems. It’s hard to do, it’s hard to justify and it’s hard to watch everyone around me “move forward” when I’m seemingly standing still. . Damn you, #lyme. . Even opening social media can’t take my mind off of it - in between the support groups and meme pages I follow I always seem to find the wedding and baby and engagement photos that my friends keep posting. I want to be happy for them, but it’s a constant reminder of where my life ISNT going right now. . How do you guys deal with this? What do you tell yourself to stay positive? I’m wondering if I need to adjust my “life goals” to something more realistic or if I just need to stay hopeful and believe that those things will come to me, too. . I could use some real talk right about now! Oh, and happy Friday

After seeing a few photos my boyfriend took of me I said, “maybe today is just not my day.” He instantly put me in new lighting and responded with, “everyday is your day.” That moment then resulted in this picture. • We may not always feel our best and the medications and diseases may mess with our appearance but at the end of the day we are stronger (more beautiful, handsome, and powerful) than how we feel inside. It’s hard being under 30 and feeling like you’re over 70. #youarenotalone • • • #lupus #lupuswarriors #autoimmunedisease #autoimmunity #sjogrens #prednisone #lasvegas #invisibleillness #chronicillness

Not all illnesses are visible to everyone. When you are living with #lupus #autoimmunedisease #chronicpain or #chronicillness you may appear as a healthy looking person on the outside but be ill on the inside especially during your #invisibleillness flare ups and relapses. Some people judge you and even call you lazy based only on what they see on the outside because they don’t get to see what happens on the inside and how difficult it’s for you to fight with your symptoms every single day trying to feel and look good. The key is to find and surround yourself with people who get you and understand your challenges and raise #lupusawareness #chronicillnessawareness and #autoimmuneawareness P. S. I would like to let you know that FREE live potent probiotic is back in stock and FREE high quality premium protein is still available! Both can be very helpful for people with Lupus and #autoimmune conditions. Protein can replenish nutrients that are often get depleted in people with lupus and #autoimmunediseases , may help with energy and supporting recovery and healing process. Probiotic can help to improve digestion and absorption of nutrients and strengthen the #immunesystem It’s truly free, no strings attached, worldwide shipping. You can get it through my website https://lupusselfhelp.com/free or jusy click the link in my instagram profile description @outsmartlupus <<<===click

: No one can truly understand what a chronic illness is like unless they actually have one. You will never understand the pain, the fatigue, the depression, the anxiety ect. Comment with a if you agree. Follow @how.u.feeling for more!