Rare Disease Day – Do You Need to Change Your Home?

Rare Disease Day always falls on the last day of February. Rare Disease Day started in 2008 on February 29th…this year it will fall on February 28th.

The goal of Rare Disease Day is to create awareness across the entire spectrum. From making individuals become more aware of rare diseases and individual struggles, to making policy makers, researchers and health professionals more aware.

Why is it important? Studies indicate that one in ten to one in 20 people will experience a rare disease at some point during their lifetime.  That’s 5-10% of the population.

Most rare diseases do not have a cure. Often research funding is lacking even though the impact of the disease may be very significant for the person affected by it. Too often researchers and policy makers will overlook rare diseases.

Health professionals may not be aware of some rare diseases and critical treatment time may be lost.

Some rare diseases may force a change in your lifestyle that may require a change in the type of home that you have.

For instance, when a person is suddenly affected by a rheumatic disease, he or she may have difficulty navigating the stairs in a home. Daily struggles with can be difficult if a person has mobility issues and lives in a multi-level home.

A ranch style home is much more conducive for the long term. A split foyer can work if most of the daily living can be done on one of the levels. It can be particularly helpful to have laundry on the same floor to prevent the struggle of climbing or descending stairs while also carrying a load of laundry.

It’s good to explore other options in the home that can make things more convenient, such as having a garage that has easy access to the kitchen for transporting groceries.

If you or someone you know is thinking that it might be time to explore moving to a home with fewer stairs, I will gladly help and I work hard to make the process as stress-free as possible.

I have a greater understanding of the challenges of a rare disease. I have a rare disease and I am very fortunate that I was diagnosed early on. My rare disease is systemic scleroderma.

Scleroderma, or systemic sclerosis, is a chronic connective tissue disease generally classified as one of the autoimmune rheumatic diseases.

The word “scleroderma” comes from two Greek words: “sclero” meaning hard, and “derma” meaning skin. Hardening of the skin is one of the most visible manifestations of the disease.

The symptoms of scleroderma vary greatly for each person, and the effects of scleroderma can range from very mild to life threatening. The seriousness will depend on the parts of the body, which are affected, and the extent to which they are affected. A mild case can become more serious if not properly treated.

It’s estimated that about 300,000 Americans have scleroderma. About one third of those people have the systemic form of scleroderma. Systemic scleroderma can cause fibrosis in the lungs, cause kidney failure, and pulmonary arterial hypertension. Interestingly, many of the most severe symptoms are very similar to severe cases of COVID-19.

Since scleroderma presents with symptoms similar to other autoimmune diseases, diagnosis is difficult. There may be many misdiagnosed or undiagnosed cases.

Actor Robin Williams noted in an interview in 2002, “You can make up a joke about almost anything,” says Williams. “But to tell you the truth, there isn’t even one tiny aspect of this disease which lends itself to humor. Scleroderma is a horrible disease…” (USA Today)

Scleroderma also has an arthritic component to it and can sometimes present similarly to another rare disease, rheumatoid arthritis. I have experienced the challenges of navigating flights of stairs when having a rheumatic flair up. It’s not fun.

I am fortunate that I can be active. I am an avid runner. If I sit for too long, my body gets very stiff. As a result, I try to stay active and typically get 10,000 steps a day. The overwhelming majority of people with scleroderma aren’t that fortunate.

Thanks for taking some time to learn about a rare disease. If you need help moving to a different home that may be better for you in the long term, please give me call and I will gladly help you.

Agent

Ron Sasso

Ron Sasso

Phone605-593-3759