“MS cannot stop you from living your life and following your dreams” – an interview with patient advocate and PatientsLikeMe member Starla Espinoza

Posted February 7th, 2014 by

Multiple Sclerosis Awareness Month is fast approaching in March, but we just couldn’t wait until then to share our recent interview with patient advocate and PatientsLikeMe member Starla Espinoza, also known as baebae. On top of being a PatientsLikeMe member since 2007, tracking her health and sharing experiences with the community, she’s also a blogger and big advocate for raising MS awareness all year round. Check out what she had to say about her supportive family, her passion for MS awareness and the simple pleasure of riding a motorcycle.

 

 

 

Can you remember what your first signs or symptoms were? And what was your diagnosis experience like?  

My first significant symptom was a buzzing sensation in my left hip. I always describe it as “a microscopic bee or hummingbird” trapped in my hip that is desperately trying to escape. It was the strangest feeling, especially since I didn’t know what was going on. My diagnosis took almost a year from the time that the buzzing in my hip started. I had more symptoms like numbness from the waist down, a tight gripping sensation around my midsection (MS hug), and dizziness for 6 weeks, just to name a few. Within a 6 month time frame, I underwent tons of testing, including blood tests, spinal taps, MRI’s of my brain and spinal cord, a CT scan, and an x-ray of my spine. I was eventually told that I had Transverse Myelitis. On December 13, 2007, I was finally diagnosed with MS. My neurologist showed me my latest MRI scans and sent me home with a bag of information and a prescription for my MS treatment to be started immediately. I cried as soon as I left his office. Within 3 minutes I heard God’s voice saying, “Don’t cry, I will never leave you nor forsake you. So do not let your heart be troubled, nor let it be afraid.”

As a mom with three daughters, how has MS impacted your family life?

As a mom of 3 girls, my MS diagnosis brought us all closer than we already were. Their names are Daesia, Dayna, and Aliya and they were only 12, 7 and 6 when MS presented itself. The girls saw me at my worst before we knew what was wrong with me. They know how to support my condition and me. My first treatment involved daily shots, and they even participated in the beginning by helping their dad care for me and give me my shots. They, along with my husband, are very active in my efforts to raise money for the MS Society every year. We bake goodies for our bake sale and we have all pounded the pavement together to solicit donations from local merchants for prizes to include in our annual raffle drawing. My girls and my husband are true MS Warriors and advocates for MS. Makes me teary-eyed just thinking about all we have done together for the past 6 years to show people that MS cannot stop you from living your life and following your dreams. My girls are now 18, 13 and 12, and they want to do everything that they can to fight MS. We are all in this together.

You mention your religious faith and passionate activism to raise awareness for MS. Can you tell us a little about that?

My story proves that God can use me. You see, God has been by my side since the beginning of my MS journey and even longer than that. He showed me His purpose for me in this MS journey. I discovered that He could use me to raise awareness for a condition that a lot of people were unaware of. A passion was sparked inside of me by God to take ownership of this cross that I had to bear, known as MS. I developed the strongest desire to tell everyone everything that I knew about MS. That even though I have MS, it does not have me. I wanted to use my voice in the most effective way possible, and He made me a patient advocate about 3 years ago. I often get the opportunity to speak at events and dinners, radio and news interviews, and now an interview here on PatientsLikeMe.  All I can say is, wow, 🙂 I’m really doing this.

It looks like you use your Multiple Sclerosis Rating Scale, and track you symptoms and treatments a lot on your PatientsLikeMe profile. What inspires you to share and donate so much of your health data with the community?

Sharing my health information with the community is part of being an advocate. If I am willing to be transparent, hopefully others will be inspired to do the same. Together, we are soldiers in this battle against MS. Sharing helps me track important health information and improve research about this disease. It’s very easy for me to do, and I can even do it from my phone. In turn, it benefits us with new treatments and ways to deal with MS. I get excited just thinking about it. Tears again, oh my.

For those who might not follow your blogs yet, can you share what they’re all about?  

My oldest daughter Daesia gets credit for the creation of my MS blog. She was 12 when I was diagnosed and after 2 years, she started to realize that most of the people she encountered had never heard of MS. Her peers and teachers had no idea what it was. She wanted me to blog about how MS personally affects me. I was already a blogger so it was a no brainer. Daesia named my blog, Did I Mention My MS. What a genius idea for a 14 year old! In my MS blog, I share personal details about my MS journey. I even shared a post that Daesia wrote for a school paper.  Wow, it sure does give me a lot of insight about how she viewed MS in her young mind. My blog posts include information about my MS treatments, medications that I take to combat the side effects of MS, what I’m doing in my community to raise funds and awareness, personal struggles with doctors and how I fought for my rights at work as someone with an “unseen” disability. It’s all about the good, the bad and even the ugly issues that I have personally dealt with as an MS patient.

What’s it been like to connect to others living with MS on PatientsLikeMe?

The first time I heard about PatientsLikeMe, I thought, “What a great idea!”  Connecting with others who live with MS on PatientsLikeMe has been super beneficial in so many ways. MS patients are sooo resilient because after all, MS is not limited to one area of our bodies. It affects us from head to toe, physically and emotionally. We draw so much strength from each other, and PatientsLikeMe gives us the platform to share how we cope with everything from new treatments, clinical trials and social security disability benefits, to name a few of the topics discussed in our forums. I have even established a relationship with a patient who lives in my area via PatientsLikeMe, and she has even joined my walk MS team, The MS Warriors. I love the fact that PatientsLikeMe brings all kinds of patients together. I have shared the PatientsLikeMe website with so many people, including a friend fighting bipolar disorder and even my husband, who struggles with chronic pain.

Finally, we see that you like to ride motorcycles! Awesome! Tell us about your travels on the open road.

Aww, the joy of riding a motorcycle. I ride with my husband and it is such an exhilarating, invigorating and therapeutic experience, all at the same time!  We live in Northern Nevada (Reno/Sparks), and with the mountains in the background, we discover some of the most beautiful and picturesque scenery on the “open” road. You have no fear; it’s like flying like an eagle (the symbol often seen on motorcycle clothing and gear). I started out riding with my husband as a passenger until he bought me my own small bike for my birthday. It was only 550 cc’s, and he taught me how to ride it. Before I knew it I was following him on his 1850 cc Harley Davidson Electraglide Classic around town. I used to love it when we would go to downtown Reno. You see so much more when you are on a motorcycle. After 3 years, I sold my bike, and now I am a passenger again on my husband’s big (custom painted) Harley Davidson Electraglide Classic. We even have matching helmets to match our bike. Not meaning to brag, but a motorcycle enthusiast such as myself cannot talk about riding motorcycles w/o specific details. This gives the whole experience to non-riders and understanding to riders. Sometimes we ride in groups and take trips to Lake Tahoe, my favorite place. Surrounded by tall pine trees, cabin homes and casinos with the lake in the background makes the drive such a vibrantly wonderful experience. Every year in Reno, NV there is an event called Street Vibrations. It’s all about motorcycle enthusiasts. People travel from all over the country, sometimes on their bikes alone or in a pack with their club. It is a loud 3-day event, and we always look forward to it every year.


2 Comments

  1. I am proud to say I. Am Starla’s Mom and this has always been an experience I will never forget of course From my point of view MS is a very unwelcome presence in our lives but Starla has taught me so much about real courage in the time of storms I pray that God continue to use her as his vessel of encouragement to others with this illness “you go baby girl !” For you are a warrior I’m every sense of the word Mommy loves you.

  2. For many or most of us, chronic diseases like MS, PD, CFIDS, FMS and other cognitive, immune and neurological diseases result from unfortunate combination of gene variants and toxins. These include biotoxins like lyme, chemotoxins like pesticides, metallotoxins like mercury, mycotoxins like molds, exitotoxins like MSG, and more. The gene variants are those that impact methylation, detoxification, immune system, and other metabolic processes. When the wrong toxins come in contact with people with glitches in these pathways, we do not clear them well, and they trigger inflammation, which is the root of all chronic disease. Inflammation in turn can open us up to infections of various kinds, which create additional toxins.

    To recover our health, we need to discover and uncover the sources of the toxins, and learn more about our gene types, and how our bodies are functioning in terms of allergies, food and chemical sensitivities, digestion and nutritional absorption, that are markers and results of healthy functioning and of problems that result in chronic diseases.

    We are in the early stages of building a Coalition for Good Health, that will work to unite people around a vision and framework for promoting discovering, uncovering and addressing the common causes of chronic diseases. Everybody has different factors involved, it is likely that they vary, but commonalities emerge.

    For example, a number of people have recovered from the diseases mentioned above when they found out they had gene glitches that make them especially susceptible to mercury toxicity. A number got better, in whole or part, working with a team of a biologic dentist and a skilled allergist, functional medicine or integrative MD. Biologic dentists test for biocompatibility of dental materials, safely remove it when indicated and minimize re-exposure with stronger protocols, ventilation, techniques and safety equipment than a simple dental dam. Functional medicine and integrative MDs can diagnose and treat problems somewhat along the lines of how a mechanic runs diagnostics and fixes acar. Test for proper functioning, review the owner’s manual (gene variants), and make adjustments and tuneups to get everything humming again.

    The Coalition for Good Health is working to spread awareness of the role of genes and toxins in triggering and treating chronic diseases. It is convened by Hidden River Health Challenge and the International Academy of Oral Medicine and Toxicology. If you would like more information, please contact me. Thank you!

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