Although I am not physically able to walk in the second annual Iowa Walk for Lupus Now, I am still very passionate about the mission of the Lupus Foundation of America, so I am participating as a virtual walker and committee member.
This organization works to fund Lupus research, support Lupus patients, and raise Lupus awareness. This year’s walk will take place on September 13th at Gray's Lake in Des Moines, IA. I would like to invite you to help support us in fighting Lupus by sponsoring me with a donation. Click the link below to visit my page:
https://www.kintera.org/faf/donorReg/donorPledge.asp?ievent=272038&lis=0&kntae272038=FA91F2962504479BB04BBD0F4718C712&supId=185223504
Kendra Isola
webmaster@cure4lupus.org






You have my support, hands up!
customs572
I wish I was able to donate. I think it is great that you are fighting for this cause that so many people battle with daily. I hope a cure is found soon. ***HUGS*** Take care.
Ellocin
I have worked night and day, within my own limitations, dealing with butt head doctors, and contributions in the hundreds now for The ALR, and Lupus Foundation of America, plus local North Texas Chapter donations, but now am near bankruptcy, and cannot contribute to any more than I do already, albeit with far limited funds. My daughter and wife cannot "walk" anymore, so we tend to contribute to our daughter's own walk group, and I have researched both my daughter and wife's separate conditions until I am near exhaustion. I find many or most people don't care about lupus suffereres, and some just turn a blind eye to the whole thing. So I do what I can. Sorry I've been very limited to any more efforts in this regard. My cup runneth over with tragedy. Sincerely Goliad
Goliad