MS is a condition that occurs when the body attacks the central nervous system. One million Americans are estimated to have this condition. Symptoms can range from numbness and tingling to speech problems, tremors, and vision issues.
Research is essential to understand better MS and the people who are affected by it. To conduct successful studies, researchers must find willing volunteers. This means finding individuals who will be suitable for clinical trials.
In our whitepaper, we provide insights into the patient population of multiple sclerosis that can help advance this mission. By surveying MS patients to learn about their experiences, what they want to gain from participating in research, and other factors that could influence their views on clinical trials, we can provide valuable information. This will help sponsors reach out and connect with patients personally, ultimately saving time and money. Download the whitepaper for free by clicking the link below.
Resources for Melanoma Patients
MRA’s Melanoma Exchange is another resource that’s worth mentioning. This community was created for patients and caregivers to exchange insights about their diagnosis, treatment, clinical trial experience, and more. This online group is a great resource for anyone affected by melanoma. It can answer questions on melanoma stages, how to manage the condition and much more.
Melanoma trials are enrolling people and they need to be involved. Start searching for clinical trials today if you are considering one. You can find a clinical trial by answering a few simple questions in the Clinical Trail Locator of the MRA or by clicking on the button below.
