Episode 15 of Through MYeloma Eyes explores how to search for trustworthy information after a cancer diagnosis without becoming overwhelmed. Solomon guides listeners to prioritise their health team, reputable organisations, and supportive communities while avoiding late-night panic, miracle-cure claims, and harmful comparisons.

This episode offers practical advice on setting limits, asking questions of your care team, and choosing information that helps you stay present and sane through uncertainty.

In this episode Solomon Alexis shares an honest, unfiltered look at life after a multiple myeloma diagnosis, covering pain, sleep, mobility, emotions, finances, friendships, and daily routines.

He gives personal ratings for symptoms like pain, neuropathy, fatigue, and mobility, explains social and financial impacts, and describes what improves his quality of life — concluding his current overall quality of life is 7 out of 10.

Through Myeloma Eyes offers lived experience, resilience, and practical perspective for anyone navigating cancer.

Host Solomon Alexis shares a personal account of getting shingles while living with multiple myeloma, explaining how a weakened immune system and cancer treatment can allow the virus to reactivate and cause severe nerve pain and a one-sided rash.

He urges listeners not to ignore sudden rashes, to seek medical attention early (including antivirals), and to pay attention to bodily warning signs, as minor symptoms can reveal larger health issues.

Host Solomon Alexis explains why he began podcasting about his multiple myeloma — not to be brave or to set an example, but as a personal pressure valve and a way to breathe.

He contrasts public sharing with private coping and stresses that neither is morally superior.

The episode mixes honesty and quiet humour, reminding listeners that laughter and vulnerability can both help, but staying private is equally valid. The central message: cope however you need to—your journey is real whether you speak about it or not.

In this episode the host answers common questions about living with multiple myeloma — covering the current lack of a cure, treatment progress, and the reality of maintenance therapy after a successful stem cell transplant.

He discusses practical lifestyle topics like diet, vaccinations (including repeat shots after transplant), ongoing medications, main side effects such as fatigue and neuropathy, and how the disease has affected travel, work, and relationships.

The episode also shares personal coping strategies, the role of family support, the cautious view on alternative therapies, and a message of hope, connection, and continued conversation.

In this episode of Through Myeloma Eyes, Solomon explores the confusing question "Why me?" as he examines known risk factors for multiple myeloma—age, race, gender, workplace exposures, obesity, family history, and past infections like H. pylori—while sharing his personal experience and reflections. Honest, personal, and a bit light-hearted, he admits that despite deep research, the exact cause remains unclear, but life and resilience continue.

Solomon shares his post-stem cell transplant results — a complete metabolic response confirmed by scans, biopsies, MRD testing and blood work — and explains the next medical steps, including consolidation therapy.

He also recounts his first trip home to Saint Lucia 143 days after transplant: the careful preparations, travel anxiety, a heat wave and a persistent cough, and the quiet courage of choosing to live fully while staying cautious.