I'm looking to interview someone with SPMS to discuss how they first noticed that their disease had progressed from the relapsing-remitting form, how they confirmed it, and how their treatment has changed.

Good Day, People with secondary progressive MS often describe the shift from relapsing to remitting as a slow creeping change rather than a sudden event. There is a weak, balancing, or fatigued symptom which starts to deepen, but the patient notices the absence of the acute flare-up. In most cases, the progression is especially concerning when the patient's neurologist examines MRI's periodically, then scans and evaluates the longitudinal function of the patient, then ascertains the absence of new relapsing and relapsing forms. In terms of treatment, the switch is most of the time no longer relapsing, but rather the attempt to fending off the steady progression with siponimod or other dissimilar medications while also trying to augment physiotherapy relapses, then striving to lessen the steady progression of unchanged symptom management. Hearing directly from someone about those first signs, how they felt using the treatment, and how the rest of day routine seems to center around deals the matter more intriguing. If you decide to use this quote, I'd love to stay connected! Feel free to reach me at gregorygasic@vmedx.com and outreach@vmedx.com.