Selena Gomez Shares How Lupus Medication Causes Her Hands to Shake – E! Online
“After I got out of the last treatment center, I knew what made me happy,” Selena explains, “and it was connection.”
But, per her doctor’s orders, Selena’s planned philanthropic visit to Kenya to see the schools she helped raise money to build was delayed several years due to her 2017 kidney transplant. Once she’s finally apple to make the trip in 2019, she vowed to visit quarterly
“The truth is I’ve never felt good enough,” Selena admitted. “Even when I’m on stage in front of a crowd, I’ll always find the one person who doesn’t like me and I believe them, I want to believe in myself. The people I’ve met here in Kenya are so giving, I just want to feel like I deserve to be here with them.”
During her time in Maasai Mara, Selena bonds with the students, talking about love, ambition and, in a particularly emotional conversation with one woman, suicidal ideation.
After her time in Kenya, Selena travels directly to London and Paris to promote her music, but she struggles to adjust to her life as a celebrity. “It just seems like such a waste of time,” she said. “What am I doing right now?”
Later acknowledging that “part of my heart is still in Kenya,” Selena admitted, “I felt guilty being there sometimes. I hate that, I feel like I went and filmed and I experienced, but it’s just so hard because I feel so selfish. Do I feel great? Yes, and do I feel like I left an impact? Yes, but do I feel like I’ve done enough? No.”
“Talking to someone about mental health in Kenya, that’s beautiful,” she continued. “I don’t know if I felt like, ‘Oh, I did it and I’m such a great person.’ No, it’s just the beginning for me.”
Source link When pop star Selena Gomez revealed her battle with lupus in 2015, many of her fans applauded her for becoming a prominent advocate for the disease. Now, in a recent Instagram post, Gomez has opened up about the reality of living with lupus, in particular, the side effects of her medication.
In a post on Instagram, Gomez shared a video of herself with a serious and calm voice. In the video, she told her fans, “Side effects of lupus include uncontrollable shaking in my hands so that’s what’s happening in the first video.” Gomez then showed herself in an interview, with both of her hands shaking.
Gomez added, “My health is what I live for, and I try to be as open and honest about that as possible. For all those out there living with an autoimmune disease, I want you to know that you’re not alone and it’s OK to feel the way you do. Let’s keep fighting, keep smiling, and let’s keep living.”
The revelation is an important reminder to Gomez’s fans of the physical struggles those with lupus must often face. Gomez’s candor about her battle has allowed her to become an inspiring representative for the 1.5 million Americans that suffer from a lupus-related illness or condition.
Gomez’s courage in sharing her story has resonated with many of her fans, and has provided an important reminder of the physical hardship those with lupus must often face. It is clear that her honesty and advocacy are a powerful reminder that those with lupus should never be silent about their struggles or their triumphs. In the words of Gomez, “Let’s keep fighting, keep smiling, and let’s keep living.”
