Well, Happy New Year all! I know it’s February, but it’s been quite some time since I’ve posted and I haven’t had the pleasure of sharing those words with many of you. I hope all has been well in your lives and for those struggling today (with Lupus or any other autoimmune condition) I hope today’s post brings you some life and encourages you to tackle your day in the best way possible–for you! Continue reading Balanced (The Resolution for Women Reflection Series)
This weekend my family, friends, and colleagues supported me as we walked with the Lupus Foundation of America to find a cure for Lupus! I have been fundraising for a little over a month now and thanks to everyone who made a contribution, my team was able to raise over $1,500 towards Lupus research! It was amazing seeing so many people working and walking together for the same cause! I look forward to continuing this work and I am praying that with continued awareness, advocacy, and fundraising efforts, this world will someday soon be a world free of Lupus!
Now that I’m back at work, I have to get readjusted to my schedule. I didn’t get a chance to post yesterday, but hey, it’s never too late! I I hope you all are keeping up and continuing to reflect on your blessing daily! One thing that I noticed this week is that my 5 things have nothing to do with my Lupus…that’s because this week was one of the most normal weeks that I’ve had in a long time! Praise God! Now, I did have a doctor appointment and a pulmonary function exam on Tuesday, but they both went great! While I am so grateful for improved health, there were so many other awesome things happening this week too–I didn’t know where to fit health news! I guess it doesn’t matter since I found a lovely spot here:D Comment below and let me know of some amazing things that happened to you this week!
Yesterday was one of the most beautiful days New York City has seen in a while! The sun was shining, there was a light breeze in the air, it was between 75° and 80° for the majority of the day, everyone that I encountered was in such a positive mood–just beautiful! I woke up early and headed straight to the hospital for another follow-up appointment with my rheumatologist and a pulmonary functions exam. Thank God, things are beginning to come back normal (back to how they were prior to my hospitalization) and I’m able to do more and more each day! Following my doctor appointment, I had plans to visit an old co-teacher that I hadn’t spent time with in a while, but first, I had to run an errand with my mom. By the time I made it to the upper west side, I was bit tired! Ironically, when I got to my friend’s apartment, both of her kids were taking their naps…the life right?! This got me thinking…why don’t adults get to take naps during the day?! Especially people like me with Lupus. I’m sure napping during the day has its benefits…
Being diagnosed with Lupus, or other autoimmune diseases, doesn’t only affect the patient, but the people in their lives as well. One of the most challenging yet necessary tasks that is given to friends and family members, is the task of giving support. When you love someone dearly, it is only natural for you to want to do all that you can to help them feel love and encouragement. To some, this may come naturally, and to others…not so much. Take my mom for instance, from my perspective, my mom handled my diagnosis so well! She never shed a tear (or so I thought), she was always there when I needed her (and still is), and was always prepared with a word from her heart to provide me with encouragement. This post is less for patients and more for friends and family members of them. What are some “Dos and Don’ts” for supporting someone with Lupus?