#PapitoForever

MOST RECENT

Support s everything niggaz know how i rock💪🏽 #papitoforever @papitoforever12 good lookin bro @dharivintich

Make Sure U Follow @papitoforever12 For The Latest Hoodies n Shirts Available ..... #PapitoForever #PapitoForever12 @papitoforever12 @papitoforever12

With The Bro @livinlifesteve always a fucking good time ... #PapitoForever #PapitoForever12 @papitoforever12 .... @cm_joelalberto dime Ave 😂😂😂

🤔🤔🤔 Can I Relate .... Ummm Let me Ask The Bro @livinlifesteve To See 🤷🏻‍♂️🤷🏻‍♂️ .... #PlayRoomNyc #MadeInMexicoRest #PapitoForever #PapitoForever12

Big bday shout of to my guy “that boy money” #PapitoForever #EverythingFunny #Evant

El que no tenga Flow que se Muera @papitoforever12 @dharivintich @livinlifesteve 😅🍺🍾. #Fracatira #papitoforever #papitoforever12

ᴘᴇʀᴍɪᴛ ɢʀᴀɴᴛᴇᴅ.
#papitoforever #papitoforever12

El que no tenga Flow que se Muera @papitoforever12 @dharivintich @livinlifesteve 😎🍺🍾. #Fracatira #papitoforever #papitoforever12

#Drip 💦💦..... Might Just Change My Name To #RockStarPapito while the bro @livinlifesteve is the #CalmPapito .... #PapitoForever #PapitoForever12

Another year, another Lupus Walk down. These walks are always a reminder of how fortunate I am to still be here. I was diagnosed in November of 2013 & today marks 10 months of me being in remission. I have been going through the rollercoaster of emotions and flares since the summer started and I’m glad today I told myself to attend the walk. Running on ZERO hours of sleep, rain had my body done for and the cold made it even worse while flaring and in pain, I was still going to attend no matter what. I NEEDED to. Being surrounded by all the Lupus supporters & spoonies always motivates me to keep on going. Years later & I still can’t believe I’m able to walk a 5K with no breaks. 💪🏽 I’m tired, I’m in pain but it was definitely worth it. I walked for all my spoonies today now I have to throw myself in rice for a few 😩. On another note, HUGE shoutout to @livinlifesteve for hooking me up with the Papito gear. 💜🙌🏽
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#WalkWithUs #LupusAwareness #LupusWarrior #FuckLupus #dermatomyositis #raynauds #arthritis #scleroderma #interstitiallungdisease #gerd #sjogrenssyndrome #chronicillness #invisibleillness #spoonie #butyoudontlooksick #lupusresearchalliance #intrepidmuseum #blog #blogger #chronicillnessblogger #papitoforever #autoimmunedisease #mctd #remission #lupusremission #chronicillnesswarrior #spooniewarrior #chronicillnessawareness #chronicallyill

Another year, another Lupus Walk down. These walks are always a reminder of how fortunate I am to still be here. I was diagnosed in November of 2013 & today marks 10 months of me being in remission. I have been going through the rollercoaster of emotions and flares since the summer started and I’m glad today I told myself to attend the walk. Running on ZERO hours of sleep, rain had my body done for and the cold made it even worse while flaring and in pain, I was still going to attend no matter what. I NEEDED to. Being surrounded by all the Lupus supporters & spoonies always motivates me to keep on going. Years later & I still can’t believe I’m able to walk a 5K with no breaks. 💪🏽 I’m tired, I’m in pain but it was definitely worth it. I walked for all my spoonies today now I have to throw myself in rice for a few 😩. On another note, HUGE shoutout to @livinlifesteve for hooking me up with the Papito gear. 💜🙌🏽
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#WalkWithUs #LupusAwareness #LupusWarrior #FuckLupus #dermatomyositis #raynauds #arthritis #scleroderma #interstitiallungdisease #gerd #sjogrenssyndrome #chronicillness #invisibleillness #spoonie #butyoudontlooksick #lupusresearchalliance #intrepidmuseum #blog #blogger #chronicillnessblogger #papitoforever #autoimmunedisease #mctd #remission #lupusremission #chronicillnesswarrior #spooniewarrior #chronicillnessawareness #chronicallyill

Living My Life Like A Fucking RockStar 🤟🏽🤟🏽🤟🏽.... #RockStar #PapitoForever #PapitoForever12 #PlayRoomNyc #MadeInMexicoRest Ohhh We Working 🙏🏼🙏🏼🙏🏼

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