Email a copy of 'We’re Warriors So Fighting On Is Just What We Do' to a friend
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E-Mail 'We’re Warriors So Fighting On Is Just What We Do' To A Friend
Loading ... Loading ...14 thoughts on “We’re Warriors So Fighting On Is Just What We Do”
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I am so thankful to have found rawarrior.com. Thank you, thank you, thank you. I was diagnosed w/RA in February of 2012.
I’m so glad you found us too. Good luck Jacquelyn.
I don’t know how you stay so put together and beautiful! Thanks for all the hard work you do for us! 🙂
aww, thank you!! But I’m not really. I’m a mess, always looking for a place to sit down, and refusing to keep shoes on… But I think most of us can “not look sick” for a few moments sometimes.
Such a great idea! Thanks for working for us! It’s so hard to get your own health information. My health insurance offered a link that was supposed to provide me with access but guess what? Now when I get blood work done I get notified that there is new information and when I check it tells me that the results are withheld for privacy reasons! My results are private from me! Great! That’s helpful! (Sorry, missing my sarcasm font again.)
yep, this is what this blue button issue is about – having full access to our own information! hello?
Kelly
Your tireless crusading is amazing!!! I feel so renewed and full of hope every time I read RAW! Today, with the blustery weather and the students acting up, my body feels like I did back-to-back marathons. After sneaking a break to look at your blog, I feel like I just received a pain-relieving, energizing shot in the arm!!! Keep on keepin’ on, Kelly!!
aww, thank you!! We are all doing our “marathons” where we are each day! We just keep going, but it’s so nice to feel understood too. Hang in there!
Thank you for all of your hard work for us! I’m not clinical but I have high RA Factor and Anti-CCP, so seeing my Rheumy every 3 months. I am one of the unlucky one’s (25%) that also has Fibromyalgia to deal with. For some reason it showed up first.
Hi Kelly – Thank you for using your limited energy to make a positive impact on so many RADer’s. I so appreciate you for going to DC and fighting for me and all of our warriors. I admire you and cannot thank you enough for the much needed support group. Love and prayers to you.
Kelly, your feet are beautiful. Thank you for your passion and hard work. You are an encourager and an inspiration. I am 30 years into this disease. No more bare feet for me. 🙁
Kelly – sorry for the segue, but I saw the RA awareness card on your site, and looked for it on the RPF site but found it not. Where can I get the PDF so I can make a bazillion of them???? Thanks for EVERYthing!!
LOL. You must have seen them on the newsletter? The first ones are being printed now on business card material so we can send them to RPF members. And YES, we are also putting the pdf up on the http://rheum4us.org site asap so you can print as many as you want. Please check there soon – hopefully within a day or so.
Kelly, Thank you for all you do. It amazes me how determined and ambitious you are! By the way, you are so photogenic-don’t think I’ve ever seen a bad picture of you! I want to say “you look so healthy”, but of course I know better!