MultipleSclerosis.net

A community for people affected by multiple sclerosis. Learn, share, and connect with peers and healthcare professionals.

[MultipleSclerosis.net @MS_HealthUnion]

“It sure didn’t feel like my disease was in remission, even though my relapse was over,” Devin writes: https://t.co/0dlkWuEuF5 #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

“When someone is diagnosed with MS or a chronic disease, we may not know what to say or do,” Dixie writes. “Start with empathy.” https://t.co/et7tcaZwb4 #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

Mike talks about trying to figure out whether symptoms are MS-related, or something else: https://t.co/H42ogyr6mB #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

“Stress is bad. It’s bad for everyone, but it’s really bad for people living with multiple sclerosis (MS),” Matt writes: https://t.co/bFmUIDFwN3 #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

New forum!
"I'm not diagnosed but have been having some odd visual disturbances for the last week. My vision has had a rippling water effect, bright flicking circle, flashes appearing right in the corner over half my eye... Read more here: https://t.co/wCsP1eX8kz... #ms

[MultipleSclerosis.net @MS_HealthUnion]

“I was worried that I would fail. But I’m very pleasantly thrilled that I’m thriving instead.” Lisa offers tips for working with MS: https://t.co/6M8Ei1Cz9Z #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

Devin talks about what it could mean when MS symptoms have worsened, but an MRI still shows no changes: https://t.co/YjDBvpRWaU #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

“Most of us have had the experience of someone who keeps forgetting that we are a person living with multiple sclerosis,” Anita writes: https://t.co/MNeW6RQPgB #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

When Matt sat down to think about where things went wrong, he realized why his anxiety and depression had worsened – and what he could do to help manage it: https://t.co/6zOEWkt8Mn #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

“I was diagnosed with MS when I was 21. I’ve now lived with MS for longer than I lived without it,” Devin writes: https://t.co/5rlRHVYr7u #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

Friends and strangers want to "help" with everything. Sometimes I don't want or need help, yet feel their hurt feelings should be taken into consideration. Do I risk making others feel dismissed by saying no thanks or instruct them how to help?
https://t.co/qmDuNVqVwW #ms

[MultipleSclerosis.net @MS_HealthUnion]

Community members share their experiences with symptoms that are worse on one side of the body: https://t.co/PfAhCnWEst #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

“I simply want all things that get on my nerves to leave me alone … and that includes all things multiple sclerosis (MS),” Dianne writes: https://t.co/zip3ijjGvd #MultipleSclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

Kim talks about setting goals and why it’s important to her: https://t.co/LcOjAHV2hX #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

Community Submitted Story: "I proposed to my then-girlfriend 10 days before I was admitted to the hospital for numbness in my legs. I sat my fiancé down and told her if she wanted an out, this was it." https://t.co/PI5RkS4SK7 #multiplesclerosis

[MultipleSclerosis.net @MS_HealthUnion]

“I decided to take a chance and try something new: working for a company full-time.” Lisa writes about working with MS: https://t.co/RsbsXbSzxU #multiplesclerosis #ms

[MultipleSclerosis.net @MS_HealthUnion]

“Most of us have bad days, so how could I discern a relapse from an extended bad MS day?” Jenny asks: https://t.co/OWUwDZMtbs #multiplesclerosis #ms #thisisms #mswarrior

[MultipleSclerosis.net @MS_HealthUnion]

“Often referred to as ‘cog fog,’ the cognitive problems that I’ve developed because of MS have had a profound impact on my life,” Devin writes: https://t.co/SRjg1oJV4T #multiplesclerosis #ms #thisisms #mswarrior

[MultipleSclerosis.net @MS_HealthUnion]

“Reading about his diagnosis didn’t push me away from him – it made me want to know more about him.” Dixie talks about dating and MS: https://t.co/J49aPSIsTf #multiplesclerosis #ms #mswarrior #thisisms

[MultipleSclerosis.net @MS_HealthUnion]

“How can I not think ‘what if?’” Dianne worries about her daughter having MS, too: https://t.co/D9XS7Th7Uv #multiplesclerosis #ms #thisisms #mswarrior