Join me on 10.16.2021 for the virtual Walk to End Lupus NOW! Dress in your purple best and send me photos/videos of you supporting me & this great cause.
Everyday is a mystery, but I hope that one day we'll find a way to help combat it completely. Funding for research and medicine is key, so I hope you'll help me make it one step closer to having more good days than bad. If you can donate anything, even $5, all the money goes to the LFA - an organization close to my heart.
I was diagnosed 16 years ago, so I've been living with SLE for over half my life. I don't like to always show how I'm really feeling when I have aches or my "wolf" patch or the constant fatigue, but my positivity has gotten me through so much. I have started a monthly infusion and am at my lowest prednisone dose that I've ever been at. I know a lot of others know that med struggle and I hope events like this continue to help and maybe one day we'll find a cure!
Especially in the past year, it’s been so difficult trying to navigate through this and covid and wondering if one minor thing I do will affect my routine. I just want to help to be part of the solution and would love for you to be part of it too!
We got this! I truly believe my friends and family are in full support and I feel so lucky to have that.