My Lupus Project

My Lupus Project:a site built around community forums for the patients, families and friends affected by autoimmune diseases to share and support each other.

[My Lupus Project @mylupusproject]

I can’t believe that I’ve waited so long to get into #TheAmericans #sogood #flareday #bingeworthy #autoimmunelife

[My Lupus Project @mylupusproject]

My #CBDoilconsultant Get yours today!!

[My Lupus Project @mylupusproject]

My new favorite product to help with my pain and anxiety caused by #autoimmunedisease https://t.co/tm2lsD1HsX #youhavetotrythis 🌱😋

[My Lupus Project @mylupusproject]

Sometimes u do everything rt, eat the best foods, take your meds, use safe products, yet the purple monster still stirs #Autoimmuneprobz ugh

[My Lupus Project @mylupusproject]

https://t.co/BtNoJJL8Aj I cant say enough about what #HempworxCBDOil has done 2 help my arthritis. I now want everyone 2 see the benefits!

[My Lupus Project @mylupusproject]

@KamalaHarris I saw the bill &I could lose my insurance!I’m a chronically ill single mother of two working PT. #voteNO #saveACA #savelives

[My Lupus Project @mylupusproject]

First vacation since I started showing symptoms over three years ago. #autoimmunewarrior #lupusstrong #livinghealthy #wontstopcantstop 💪🏽💜

[My Lupus Project @mylupusproject]

Yes Im #bingewatching #houseofcards today cause Im on bed rest #thankslupus #glasshalffull #Underwood2016 #dougstamper 😳#LupusWarrior 💜💜💜💜💜

[My Lupus Project @mylupusproject]

#truth #iloveyourhonesty #flaredays https://t.co/8usMlw79uF

[Dan Walmer @Thrown4aLup]

#WhenIFlare I want to eat all the things. And lay on my couch like a beached 🐋. A beached 🐳 that likes ice cream. Just being honest. 👀

[My Lupus Project @mylupusproject]

#PutOnPurple

[My Lupus Project @mylupusproject]

#lupusawareness #wearpurplefriday #lupuswarriors

[My Lupus Project @mylupusproject]

The weather is gloomy as am I! #flaredays #lupuslife

[My Lupus Project @mylupusproject]

I think it's that time for me today! #Happy420 #thinkgreen #takepuffsnotpills #medicinalcannabis

[My Lupus Project @mylupusproject]

Wondering how many people out there have had their #autoimmune diagnosis changed several times. I just had a second #positivescl80ANA

[AstraZeneca @AstraZeneca]

New treatment strategies may improve patient’s outcomes in #lupus, and there is a great need for new treatments for #lupus #LupusACA

[My Lupus Project @mylupusproject]

Just another manic sick day 😷 ugh. #autoimmunedieasewarrior

[Dan Arnold @nrf2dan]

"Don’t be afraid your life will end; be afraid that it will never begin." ―Grace Hansen #quote #inspiration

[Scleroderma News @SclerodermaNews]

Sunbathing Naked, and Other Unsolicited Advice for Scleroderma. Read more >> https://t.co/Z0KYbQuZog

[Scleroderma Canada @SclerodermaCAN]

The obscure disease Ray mentions in this week's episode of @lenadunham's @GirlsHBO is the one 16,000 Canadians struggle with: #scleroderma