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.