My June Experiment: A Chronic Voice Linkup

Welcome to my June experiment. My life will only get worse unless I try something different. Here’s what I intend to try this month to make living with the progression of fibromyalgia, arthritis, and endometriosis better.

Sharing – Word of the Week

Sharing is caring and that is what I am doing, not just this week, but all month long for fibromyalgia and arthritis awareness!

Psoriasis and Psoriatic Arthritis Connection

🧐 1 in 3 people with psoriasis may develop psoriatic arthritis. Learn more about it here!

Word of the Week – Adjusting

Everyone is currently experiencing some form of adjustment. But for the chronically ill, it’s just part of everyday life.

Living with Pain, Misunderstood and Ignored

Chronic pain is misunderstood by our family, friends, doctors, and even ourselves. If not careful those misunderstandings could lead to more pain.

What COVID19 and Social Distancing have Returned to the Lives of the Chronically Ill

COVID19 and social distancing have taken a lot away from us, but there are a few things they have given the chronically ill that are worth celebrating!

How COVID-19 has Changed the Lives of the Chronically Ill

COVID-19 has changed our lives in ways we never imagined. Let’s take a look at how it has impacted life with a chronic illness.

Spring Clean: Disinfect Your Diet

It’s time to spring clean your diet! How journaling helped me weed out the foods and ingredients that were increasing my chronic pain.

Spring Clean: Spruce up your view!

Today I am going to present you with a spring cleaning idea that you may not have thought of……. sprucing up your view!

My Word of the Week is Limited * How My Current Chronic Pain Flare is Limiting My Time, Energy, Ability, and Patience. How I am Getting By without Giving Up!

My current chronic pain flare has limited my time, energy, ability, and patience. This is how I am getting by without giving up.

Your Flare Will End In 5 Days! Would a Recovery Time Frame Make Getting Through Your Next Chronic Pain/Illness Flare Less Frustrating?

Lack of a chronic pain/illness flare recovery time frame leads to frustration, guilt, and depression. Is having one unrealistic? It may not be!

Word of the Week * TIRED * Living with Incurable Abdominal Chronic Pain

My word of the week is TIRED! Unless someone lives with chronic pain, they have no idea how tiring it can be or how long it takes to recover from a flare.

My Valentines Day Wish For All of You Chronic Pain Warriors Who Fight a Battle that NO ONE Understands

A Valentines Day wish from me to you, someone who understands and knows all too well how exhausting living with chronic pain can be!

What The Disabled Diva is Looking at, Playing, Joining, Invigorated by, and Ditching This Month. Living with Fibromyalgia and Psoriatic Arthritis

In this month’s linkup I share what I am looking at, playing, joining, invigorated by, and ditching to make living with my chronic illnesses easier, less painful, and more fun!

The Mandalorian Approach to Explaining What it is Like to Live with Fibromyalgia and Psoriatic Arthritis

Have you watched The Mandalorian on Disney Plus? My family had a weekly date to watch it together. Afterward, we would discuss the episode or show in general. One thing that surprised me was how deeply I related to the Mandalorian whenever he was questioned about not removing his helmet. What does this have to do with living with fibromyalgia and psoriatic arthritis? Read on to find out!

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