recent posts
- 🪶Feathered Friends | Three Gulls and a Road Trip: Waterbirds of the Pacific Coast Highway
- ⚾ Game Day Stories | Three Stadiums, One Coastline, and A Whole Lot of Baseball
- 🧡 My MS Journey | You With The Sad Eyes A Memoir by Christina Applegate
- 👟 The 10K Chronicles | June Steps on the West Coast
- 🪶 Feathered Friends | West Coast Birding on the Pacific Coast Highway
Category: MS Journey
MS Journey is where I share the personal stories, reflections, and lived experiences that shape my life with multiple sclerosis. These posts highlight resilience, daily habits, advocacy, and the moments that help me navigate MS with strength and honesty.
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The author reflects on discovering the podcast MeSsy and Christina Applegate’s memoir You With the Sad Eyes, which resonates deeply due to their shared experience with multiple sclerosis (MS). Applegate’s openness about her struggles offers inspiration, encouraging a positive lifestyle change in the author while highlighting the importance of honest conversations surrounding MS.
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The author shares their experience discovering the MeSsy podcast hosted by Christina Applegate and Jamie Lynn Sigler, relating to their journeys with multiple sclerosis (MS). The podcast features candid discussions blending humor and vulnerability, focusing on MS and life. The author appreciates the balance between the hosts’ perspectives and looks forward to learning more through…
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The author reflects on the changes in their life following an MS diagnosis, highlighting the importance of community and shared experiences. Attending an MS patient event, they learned that MS manifests differently for everyone, emphasizing personal journeys. They realized the need for self-advocacy and the value of individual stories in navigating their path.
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The post discusses the author’s journey with multiple sclerosis (MS) and the impact of Selma Blair’s memoir, “Mean Baby.” Blair’s candid storytelling highlights her experiences with MS, weaving it into her broader life narrative. The author emphasizes the uniqueness of individual MS journeys and the importance of personal advocacy.
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When Doctors Started Asking About Mono During my first neurologist visit after my MS diagnosis in 2023, I heard a repetitive question. The doctor asked if I ever had mononucleosis. The same question came up multiple times during my hospital stay when the diagnosis became official. At first, I wondered why everyone suddenly cared about…
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The author shares experiences from a recent infusion treatment amidst personal turmoil. Living in Mebane, NC, the author navigates new lab procedures and a change in medical facilities. This day coincides with a family crisis as the author’s grandmother suffers a heart attack in Ohio, facing recovery challenges. Optimism persists amid adversity.
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The author reflects on the emotional and financial challenges following a diagnosis and treatment for multiple sclerosis. Despite the support from friends and family during infusions, the staggering costs—rising from $131,000 to $167,400 at a hospital compared to $96,643 at an infusion center—highlight the systemic issues in healthcare pricing.
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Palmer Kippola’s “Beat Autoimmune” emphasizes six lifestyle keys crucial for managing autoimmune conditions. The author shares her transformative journey, detailing significant changes in nutrition, gut health, stress management, toxin reduction, infection awareness, and hormone balance. This holistic approach led to remarkable improvements in her health and vitality.
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After months of lifestyle changes post-MS diagnosis, the author approached their May 2024 MRI appointment with cautious optimism. The results revealed healing with no new lesions, indicating significant progress. The journey continues, marked by perseverance and determination, balancing health habits with joy, reinforcing a positive outlook.
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The author reflects on experiencing persistent symptoms after a medical diagnosis, describing a particularly challenging moment at a grocery store where they struggled to maintain balance. As they navigated the store using a cart for support, they learned the importance of taking small steps forward, even amidst discomfort and awkwardness.