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Today is World Lupus Day and I'm wearing Purple the best way I know how to show support for my friend @the_ltd as well as so many others battling the disease πŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œ#POPforLUPUS #knowLupusnoLupus #LupusJamaica πŸ’œπŸ’œπŸ’œ

It's still May so you know what that means more lupus facts! Lupus patients more often than not need to be on medication to keep the disease in check, these medications ARE NOT CHEAP. Currently lupus patients are not supported by the National Health fund of Jamaica #knowlupusnolupus #lupusawarenessmonth

ThrowbackπŸ“†
Start Everyday with An Attitude of Gratitude
πŸ˜ƒπŸ˜ƒπŸ˜ƒπŸ™πŸ™πŸ™πŸ™ŒπŸ™ŒπŸ™ŒπŸ˜‰πŸŽΌπŸŽΆ
Thank You Lord.
😳😳😳😍😍😍😍😍
#knowlupus
#knowlupusnolupus
#shareloveafrica
#loveyourz

I have lupus, but lupus doesn't have me!! My hip replacement surgery went great!!!! βœ‹βœ‹βœ‹βœ‹βœ‹βœ‹#knowlupusnolupus #lhandsign #standupagainstlupus @runningforlupus @lupusorg #βœ‹

Sending love, light and prayers to my fellow #lupuswarrior @selenagomez as she recovers from her kidney transplant. Selena is an inspiration to all #lupus patients that lupus should never stop us from excelling in whatever we do--that we should keep on going not just to survive but to thrive despite the pain and difficulties. The thought that there is no cure sometimes makes me falter, but having my fellow lupies by my side makes me stronger. We are here with and for you @selenagomez πŸ’œ

Lupus is a disease that is often misunderstood. Oftentimes people with lupus look perfectly fine at the outside but inside our immune system is attacking our organs. #knowlupusnolupus
Repost from @selenagomez using @RepostRegramApp - I’m very aware some of my fans had noticed I was laying low for part of the summer and questioning why I wasn’t promoting my new music, which I was extremely proud of. So I found out I needed to get a kidney transplant due to my Lupus and was recovering. It was what I needed to do for my overall health. I honestly look forward to sharing with you, soon my journey through these past several months as I have always wanted to do with you. Until then I want to publicly thank my family and incredible team of doctors for everything they have done for me prior to and post-surgery. And finally, there aren’t words to describe how I can possibly thank my beautiful friend Francia Raisa. She gave me the ultimate gift and sacrifice by donating her kidney to me. I am incredibly blessed. I love you so much sis. Lupus continues to be very misunderstood but progress is being made. For more information regarding Lupus please go to the Lupus Research Alliance website: www.lupusresearch.org/

May 10, 2017 is World Lupus Day! Let's all join the worldwide effort and wear purple in support of raising awareness about this chronic autoimmune disease. Post pics in your purple! Spread the word, tell a friend and I hope to see you all #POPforLUPUS #knowLupusnoLupus #LupusJamaica πŸ’œπŸ’œπŸ’œ

It's never too late. #PurpleForLupus #KnowLupusNoLupus

If you didn't know, May is #LupusAwarnessMonth so here's a little #fbf of what life's been like the last two years. Left side: one of the worst times of my life ( ICU, Chemo, a lot of needles). Right side: some of the best, self explanatory. #Lupus is a chronic autoimmune disorder & it is most common among African-American females. Currently, there is no cure. It can manefest as different ailments, making it VERY hard to diagnose (trust me). Although one cannot die from Lupus; they may die from complications of it. Once people are put on the proper treatment plan, Lupus can be regulated. I now have under a year to go on my plan, so I'm looking forward to many more moments like the ones of the right πŸ’œ πŸ‘ŠβœŒπŸ˜Š#Awarness #KNOWlupusNOlupus

MOST RECENT

Sending love, light and prayers to my fellow #lupuswarrior @selenagomez as she recovers from her kidney transplant. Selena is an inspiration to all #lupus patients that lupus should never stop us from excelling in whatever we do--that we should keep on going not just to survive but to thrive despite the pain and difficulties. The thought that there is no cure sometimes makes me falter, but having my fellow lupies by my side makes me stronger. We are here with and for you @selenagomez πŸ’œ

Lupus is a disease that is often misunderstood. Oftentimes people with lupus look perfectly fine at the outside but inside our immune system is attacking our organs. #knowlupusnolupus
Repost from @selenagomez using @RepostRegramApp - I’m very aware some of my fans had noticed I was laying low for part of the summer and questioning why I wasn’t promoting my new music, which I was extremely proud of. So I found out I needed to get a kidney transplant due to my Lupus and was recovering. It was what I needed to do for my overall health. I honestly look forward to sharing with you, soon my journey through these past several months as I have always wanted to do with you. Until then I want to publicly thank my family and incredible team of doctors for everything they have done for me prior to and post-surgery. And finally, there aren’t words to describe how I can possibly thank my beautiful friend Francia Raisa. She gave me the ultimate gift and sacrifice by donating her kidney to me. I am incredibly blessed. I love you so much sis. Lupus continues to be very misunderstood but progress is being made. For more information regarding Lupus please go to the Lupus Research Alliance website: www.lupusresearch.org/

Act Now To Help Bring Awareness To Lupus!!! #Donatetoday #knowlupusnolupus #linkinbio #knowlupusnolupus πŸ’œ

#FACEOFLUPUS One of the greatest entertainers of all time. It is thought that Michael Jackson was diagnosed with Lupus in 1983, but he didn’t let any of his medical conditions stop him from getting up on stage and performing! πŸ’œ #knowlupusnolupus

βœ‹πŸΎπŸ’œ Act Now To Help Bring Awareness To Lupus!!! #Donatetoday #knowlupusnolupus #linkinbio #knowlupusnolupus

Women of color are two to three times more at risk for lupus than Caucasians. πŸ€·πŸΎβ€β™€οΈ #lupus #knowlupusnolupus

Act Now To Help Bring Awareness To Lupus!!! #Donatetoday #knowlupusnolupus #linkinbio

Never been happier, Never been prouder, Never been Stronger!
#beyondinvisible #NonStopNikki #KnowLupusNoLupus #LupusWarrior #lupus #shareyoustory #phuckdaflareups

So thankful for these people today and everyday as they stand beside and help me fight this battle. I couldn't do it without themπŸ’œπŸ’œπŸ’œ #lupuswarrior #knowlupusnolupus #lupussucks #milupusfoundation

All I can say is Bee 1 🐝is a fighter!! β€’β€’β€’#Repost @stoneflowermom
・・・
I am thanking God daily and I stand firmly on His word. Look how far we have come. The top picture is Amber approximately this time last year. The bottom picture is her August 3rd, 2017. For those that have been following our journey over the last 2 years' you know the hurdles we have cleared. For those that don't know our journey, this time last year @amberbee_good was literally in the fight for her life. She almost lost the battle several times; however, God said, not yet. To see my child today, sit up on the side of her bed, feet firmly planted on her purple rug with a smile on her face; all the while thanking God, does my heart ❀️good. She sat up for over an hour, something she has not been able to do in over a year and a half. All this has been accomplished without Physical Therapy or Occupational Therapy because the Insurance Company won't pay for it. So guess what? We are doing our own PT & OT. The lesson learned is: Don't let denials, rejections, or the word NO stop you. The journey may be difficult, however, the reward is worth it.
#HEisable #lupuswarrior #lupus365 #lupus #lupie #LFA #lupusfoundationofAmerica #knowLupus #noLupus #KnowLupusNoLupus #lupushtx #lupuslove #lupielove #lupusstrong #lupussucks #lupusawareness #cruelmystery #fourwingsfoundation #fourwingsteam #amberspurplepeople #texaschildernshospital #rheumatology

I am thanking God daily and I stand firmly on His word. Look how far we have come. The top picture is Amber approximately this time last year. The bottom picture is her August 3rd, 2017. For those that have been following our journey over the last 2 years' you know the hurdles we have cleared. For those that don't know our journey, this time last year @amberbee_good was literally in the fight for her life. She almost lost the battle several times; however, God said, not yet. To see my child today, sit up on the side of her bed, feet firmly planted on her purple rug with a smile on her face; all the while thanking God, does my heart ❀️good. She sat up for over an hour, something she has not been able to do in over a year and a half. All this has been accomplished without Physical Therapy or Occupational Therapy because the Insurance Company won't pay for it. So guess what? We are doing our own PT & OT. The lesson learned is: Don't let denials, rejections, or the word NO stop you. The journey may be difficult, however, the reward is worth it.
#HEisable #lupuswarrior #lupus365 #lupus #lupie #LFA #lupusfoundationofAmerica #knowLupus #noLupus #KnowLupusNoLupus #lupushtx #lupuslove #lupielove #lupusstrong #lupussucks #lupusawareness #cruelmystery #fourwingsfoundation #fourwingsteam #amberspurplepeople #texaschildernshospital #rheumatology

Some days are harder than others but all of them are a special gift from God. When life seems tough and rough, I remember all the great things my son brings to my life. I pray that I have planted seeds that will flourish one day. Pictures like this are the reason that I try so hard to keep fighting. Teach a child the ways of the Lord, and he shall never part from him. #HECHOSEME #JosiahGG #JosiahmeansprotectedbyGod #mysonismyworld #ilovemyson #lupussucks #knowlupusnolupus #invisibleillnesses #james112 #painmakesusstronger

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