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Everyone Welcome to share your thoughts, feelings, pain & tips. Write poetry.. prose.. spoken word to express, vent or just to get things out of your system.. share with us.Please share your cultural background & pride.
In Australia there isn't enough known about this disease. If you were to ask 100 people if they knew what Lupus was in Australia you might be lucky to get 2 responding with yes. Everyone in Australia needs to know what Lupus is and we need a better support group because there is one but it is only for states and I currently don't live in that state.
Welcome to Physicians for Patients! This is a place for new users to post questions about navigating the website and to share tips with each other.
This is a Lupus support group for those living in and around the MidWestern United States and especially Iowa though anyone may join. I would love to hear about good Dr.'s, good days, and also, if you need to rant and rave or just a shoulder to cry on; go for it!! That is why they call it support. This community is also here for the family and friends of those (like many of us) who suffer from this horrible disease but aren't quite sure how to cope!! I can refer you to some amazing websites for GREAT information! I have 5 years experience at running groups such as this so, feel free to either message me with questions OR leave me comments with questions if you have them. NOTHING is Taboo to talk about, as everything in daily life pertains to our daily struggles and how we live and survive. From laundry to sex...you can feel free to lay it all on the line in here if you need to ask for advice (so to speak) or just plain old fashioned information. Peace, Brightest Blessings & Gentlest Hugs!
We are a non-profit support lupus patients in the panhandle of Florida and southern Alabama. Join us and see what's going on in your neighborhood.
