#lupus Instagram Photos & Videos

lupus - 785362 posts

Latest Instagram Posts

  • the.real.patty - Patty Weaver @the.real.patty 27 minutes ago
  • I’m participating in the @lupusfaheartland #KCWalkToEndLupusNow on June 8. Will you sponsor me? Clickable link is in my bio: http://chapters.lupus.org/goto/therealpatty .
This post is from last year’s walk. My mom, @gatattcp,and sister joined me at the walk. It was hot as the fires of hell, but it was a lot of fun. I hope to match my fundraising from last year!
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2018 Post
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"Yes, I’m wearing a cape. No, I cannot leap over a building, lift a car, or foil a supervillain’s plains to take over the world. What I can do is fight #lupus. I physically fight it every day, and once a year I join my fellow lupies in raising funds for lupus research. .
Thank you for helping me raise $1,770 for the @lupusfaheartland Walk to End Lupus Now! With your support, Team Weaving Walkers was the #2 fundraiser at the Kansas City walk, and I got this awesome cape. Annnnnd my team won tiny, tasty cakes from @nothingbundtcakes. .
I’m still taking donations online if you want to give. Just click on the DONATE button at http://chapters.lupus.org/goto/pattyweaver.
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#thankyou #KCWalkToEndLupusNow #support #encourage #inspire #BePowerful #lupussuperhero #lupuswarrior #hope #findacure" #ipreview via @preview.app I’m participating in the @lupusfaheartland #kcwalktoendlupusnow on June 8. Will you sponsor me? Clickable link is in my bio: http://chapters.lupus.org/goto/therealpatty . This post is from last year’s walk. My mom, @gatattcp,and sister joined me at the walk. It was hot as the fires of hell, but it was a lot of fun. I hope to match my fundraising from last year! . . 2018 Post . "Yes, I’m wearing a cape. No, I cannot leap over a building, lift a car, or foil a supervillain’s plains to take over the world. What I can do is fight #lupus. I physically fight it every day, and once a year I join my fellow lupies in raising funds for lupus research. . Thank you for helping me raise $1,770 for the @lupusfaheartland Walk to End Lupus Now! With your support, Team Weaving Walkers was the #2 fundraiser at the Kansas City walk, and I got this awesome cape. Annnnnd my team won tiny, tasty cakes from @nothingbundtcakes. . I’m still taking donations online if you want to give. Just click on the DONATE button at http://chapters.lupus.org/goto/pattyweaver. . #thankyou #kcwalktoendlupusnow #support #encourage #inspire #bepowerful #lupussuperhero #lupuswarrior #hope #findacure" #ipreview via @preview.app
  • I’m participating in the @lupusfaheartland #kcwalktoendlupusnow on June 8. Will you sponsor me? Clickable link is in my bio: http://chapters.lupus.org/goto/therealpatty . This post is from last year’s walk. My mom, @gatattcp,and sister joined me at the walk. It was hot as the fires of hell, but it was a lot of fun. I hope to match my fundraising from last year! . . 2018 Post . "Yes, I’m wearing a cape. No, I cannot leap over a building, lift a car, or foil a supervillain’s plains to take over the world. What I can do is fight #lupus. I physically fight it every day, and once a year I join my fellow lupies in raising funds for lupus research. . Thank you for helping me raise $1,770 for the @lupusfaheartland Walk to End Lupus Now! With your support, Team Weaving Walkers was the #2 fundraiser at the Kansas City walk, and I got this awesome cape. Annnnnd my team won tiny, tasty cakes from @nothingbundtcakes. . I’m still taking donations online if you want to give. Just click on the DONATE button at http://chapters.lupus.org/goto/pattyweaver. . #thankyou #kcwalktoendlupusnow #support #encourage #inspire #bepowerful #lupussuperhero #lupuswarrior #hope #findacure" #ipreview via @preview.app
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  • snazzy_keto_athlete - snazzy_keto_athlete @snazzy_keto_athlete 41 minutes ago
  • I made the @all_day_i_dream_about_food brownie cheesecake for Easter dinner. I used the @bulkbarnfoods monk fruit erythritol blend and I used less than the recipe calls for. In this way I avoid the nasty aftertaste.

Hubby and I topped ours with cocao nibs and the @waldenfarmsinternational caramel topping. Its frightening how it contains no actual food, but every once in a while we eat it. I made the @all_day_i_dream_about_food brownie cheesecake for Easter dinner. I used the @bulkbarnfoods monk fruit erythritol blend and I used less than the recipe calls for. In this way I avoid the nasty aftertaste. Hubby and I topped ours with cocao nibs and the @waldenfarmsinternational caramel topping. Its frightening how it contains no actual food, but every once in a while we eat it.
  • I made the @all_day_i_dream_about_food brownie cheesecake for Easter dinner. I used the @bulkbarnfoods monk fruit erythritol blend and I used less than the recipe calls for. In this way I avoid the nasty aftertaste. Hubby and I topped ours with cocao nibs and the @waldenfarmsinternational caramel topping. Its frightening how it contains no actual food, but every once in a while we eat it.
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  • diosmayrabueno_ - Diosmayra Bueno @diosmayrabueno_ 59 minutes ago
  • #EASTERSUNDAY #LUPUS #30LBWEIGHTLOSS 
Thank you for watching ! 
Please subscribe 
If you haven’t watched my part one please check it out. I am becoming more open and vulnerable on social media so people just like me can be inspired to strive! No matter their situation they strive and are excited to get better and do more for their selves just like I want to do for my self. I’m just a girl with a purpose and I want you guys to see me on my journey 🙏🏽. God bless “You intended to harm me, but God intended it all for good. He brought me to this position so I could save the lives of many people.”
‭‭Genesis‬ ‭50:20‬ ‭

#lupus #nyc #30lbweightloss #easter #resurrectionsunday #kidneys #lupusnephritis #whensmokeclears @whensmokeclears #eastersunday #lupus #30lbweightloss Thank you for watching ! Please subscribe If you haven’t watched my part one please check it out. I am becoming more open and vulnerable on social media so people just like me can be inspired to strive! No matter their situation they strive and are excited to get better and do more for their selves just like I want to do for my self. I’m just a girl with a purpose and I want you guys to see me on my journey 🙏🏽. God bless “You intended to harm me, but God intended it all for good. He brought me to this position so I could save the lives of many people.” ‭‭Genesis‬ ‭50:20‬ ‭ #lupus #nyc #30lbweightloss #easter #resurrectionsunday #kidneys #lupusnephritis #whensmokeclears @whensmokeclears
  • #eastersunday #lupus #30lbweightloss Thank you for watching ! Please subscribe If you haven’t watched my part one please check it out. I am becoming more open and vulnerable on social media so people just like me can be inspired to strive! No matter their situation they strive and are excited to get better and do more for their selves just like I want to do for my self. I’m just a girl with a purpose and I want you guys to see me on my journey 🙏🏽. God bless “You intended to harm me, but God intended it all for good. He brought me to this position so I could save the lives of many people.” ‭‭Genesis‬ ‭50:20‬ ‭ #lupus #nyc #30lbweightloss #easter #resurrectionsunday #kidneys #lupusnephritis #whensmokeclears @whensmokeclears
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  • healthadvocacysummit - Health Advocacy Summit @healthadvocacysummit 1 hour ago
  • Heads up‼️ #takeovertuesday is happening  again! Jameisha Prescod is a writer, advocate, and journalist researcher for BBC News living with Systemic Lupus Erythematosus. She also recently graduated from Ravensbourn University London with a BA in digital film production. For more information, read a personal message from Jameisha below and make sure you check out our story on TUESDAY for a day in the life of this amazing human 💜🙌🙌🙌 . . .

Hey, I’m Jam. I’ll be taking over Health Advocacy Summit’s instagram account this Tuesday. I run @youlookokaytome an online platform for pain and chronic illness. It’s a place where I create visual content about disability, healthcare, long term conditions and how they relate to wider themes like technology, art and culture. 
I got diagnosed with Lupus in 2014 when I started university. It stopped me from being able to do the same things my peers could do which SUCKED. The frustration of the barriers I had, as well as the lack of empathy and understanding from people led me to create my platform. I really hope to create a space where not only people with chronic illnesses can feel less alone, but also a place to educate others and make the world (or at least one person) more understanding and accessible. 
I think there are many ways to be a health advocate. My way is through creative visuals, but someone else’s may be writing or artwork or music. It’s not always easy, I still have to work to support myself and juggling both along with a few chronic illnesses is exhausting, but it honestly makes me happy and feel like I’m making a difference, even if it’s a small difference. Heads up‼️ #takeovertuesday is happening again! Jameisha Prescod is a writer, advocate, and journalist researcher for BBC News living with Systemic Lupus Erythematosus. She also recently graduated from Ravensbourn University London with a BA in digital film production. For more information, read a personal message from Jameisha below and make sure you check out our story on TUESDAY for a day in the life of this amazing human 💜🙌🙌🙌 . . . Hey, I’m Jam. I’ll be taking over Health Advocacy Summit’s instagram account this Tuesday. I run @youlookokaytome an online platform for pain and chronic illness. It’s a place where I create visual content about disability, healthcare, long term conditions and how they relate to wider themes like technology, art and culture. I got diagnosed with Lupus in 2014 when I started university. It stopped me from being able to do the same things my peers could do which SUCKED. The frustration of the barriers I had, as well as the lack of empathy and understanding from people led me to create my platform. I really hope to create a space where not only people with chronic illnesses can feel less alone, but also a place to educate others and make the world (or at least one person) more understanding and accessible. I think there are many ways to be a health advocate. My way is through creative visuals, but someone else’s may be writing or artwork or music. It’s not always easy, I still have to work to support myself and juggling both along with a few chronic illnesses is exhausting, but it honestly makes me happy and feel like I’m making a difference, even if it’s a small difference.
  • Heads up‼️ #takeovertuesday is happening again! Jameisha Prescod is a writer, advocate, and journalist researcher for BBC News living with Systemic Lupus Erythematosus. She also recently graduated from Ravensbourn University London with a BA in digital film production. For more information, read a personal message from Jameisha below and make sure you check out our story on TUESDAY for a day in the life of this amazing human 💜🙌🙌🙌 . . . Hey, I’m Jam. I’ll be taking over Health Advocacy Summit’s instagram account this Tuesday. I run @youlookokaytome an online platform for pain and chronic illness. It’s a place where I create visual content about disability, healthcare, long term conditions and how they relate to wider themes like technology, art and culture. I got diagnosed with Lupus in 2014 when I started university. It stopped me from being able to do the same things my peers could do which SUCKED. The frustration of the barriers I had, as well as the lack of empathy and understanding from people led me to create my platform. I really hope to create a space where not only people with chronic illnesses can feel less alone, but also a place to educate others and make the world (or at least one person) more understanding and accessible. I think there are many ways to be a health advocate. My way is through creative visuals, but someone else’s may be writing or artwork or music. It’s not always easy, I still have to work to support myself and juggling both along with a few chronic illnesses is exhausting, but it honestly makes me happy and feel like I’m making a difference, even if it’s a small difference.
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  • kenweal - KenWeal® @kenweal 1 hour ago
  • @KennethWeal, Founder and CEO, wearing the Black, Purple & White #KenWeal Symbol Hoodie. 🦅

Pick yours up on www.KenWeal.com @kennethweal, Founder and CEO, wearing the Black, Purple & White #kenweal Symbol Hoodie. 🦅 Pick yours up on www.KenWeal.com
  • @kennethweal, Founder and CEO, wearing the Black, Purple & White #kenweal Symbol Hoodie. 🦅 Pick yours up on www.KenWeal.com
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