COVID-19 has amplified patient expectations about the quality and safety of care, particularly for the growing number of patients with autoimmune diseases. New provider alternatives for ongoing infusion and injection therapy are reshaping how and where specialized care is delivered.
Winter can be a tough time for people with rheumatoid arthritis. The cold weather can make joints feel stiff, so it can be tempting to stay put inside all season. Whether or not you are on a biologic like Remicade, Entyvio or Orencia to treat your rheumatoid arthritis, the truth is that lack of movement can make your symptoms worse, so it’s important to make moving your body a priority, especially during the winter months.
There’s so many traditions to look forward to when the Thanksgiving holiday rolls around – from the Macy’s Thanksgiving Day Parade to the traditional dinner feast to endless hours of football. However, if you’re one of the many people living with IBD, traditional Thanksgiving foods might be the tradition you look forward to the least.
October 29th is World Psoriasis Day — an annual day dedicated to raising awareness for the people living with psoriasis and psoriatic arthritis. In the US alone, it’s estimated that over 8 million people live with psoriasis.
The month of September celebrates yoga — an ancient practice combining physical, mental and spiritual strength — which many people find challenging, yet incredibly rewarding for their mind and body. It’s no surprise that yoga is known to be a beneficial practice in people’s lives, but it’s also one of the most commonly recommended exercises for those living with multiple sclerosis.
Many people are finding this summer with the outbreak of COVID-19 abnormal at best, but it can be especially challenging for those living with Crohn’s disease as they have to be extremely careful to avoid exposure to COVID-19. As we enter into the home stretch of the summer months, we’re taking a deeper dive in how to live well in the heat, sunshine and Coronavirus while managing Crohn’s disease.
When someone has migraines more than 15 times monthly for several months at a time, doctors typically classify this as chronic migraines. Finding the right balance of medicine, treatment and likely triggers to manage this condition can be overwhelming.
As important as it is to stay active while living with MS, it’s even more important to exercise safely. During the heat of the summer, that means taking extra precautions to ensure you break a sweat while keeping yourself safe and healthy.
With the growing cost of care – especially for specialty pharmaceuticals like biologics – combined with new health plans designed to shift more of the financial responsibility to patients, every penny counts. Worrying about covering healthcare costs shouldn’t be at the forefront of anyone’s thoughts. Fortunately, there are a number of non-profit organizations and drug manufacturers that provide patient assistance programs (PAPs) to help shoulder some – and sometimes even all – of the financial burden.
As patients navigate the day-to-day of chronic disease management, it can be difficult to track medication, manage symptoms, and receive the support they need to live a healthy and fulfilled life. Fortunately, several companies took note and introduced apps to help patients understand, manage and provide insights into their condition.