Lupe and Brian talk about brain Fog, It comes it goes. The feeling of not being able to communicate with confidence in today’s topic.
Lupe and Brian talk about Lupe’s recent travels to Mexico and how she managed her symptoms for a week of air travel and activities.
Lupe sends greetings from Guadalajara and Brian talks about 5 items that have helped alleviate some of Lupe’s complaints regarding having Sjogren’s Syndrome.
Lupe and Brian share some exciting information about new support groups. The first being with the Sjogren’s Syndrome Foundation of America and the second a MeetUp group called “Chronically Active”
Lupe and Brian speak with Cristina Montoya, the Arthritis Dietician.
Lupe and Christina have been talking on Instagram and her knowledge, experience and Sjogren’s journey is remarkable.
Lupe & Brian discuss a few realizations in regards to Sjogren’s Syndrome they had grieving the loss of Ali, the family dog of ten and a half years.
Chair of the Board of Directors and keynote speaker for the Sjogren’s Syndrome Foundation, Janet Church joins us this week on “Sjogren’s Strong”
Her journey with Sjogren’s is unbelievable and you will not want to miss it!
Brian and Lupe wrap up the 2019 L.A. Area Walk for Sjogren’s this past Saturday.
This episode discusses the added workload that was put on Lupe as Brian fought off an illness over the weekend. These little things we didn’t think of, but if we had, we could have planned for an easier experience for Lupe.
Susan Barajas joins us in the studio to talk about her journey and involvement with the Sjogren’s Syndrome Foundation.