Cultivating Kinship on Social Media

By: Stacie Prada

An estimated 2.8 million people worldwide are living with Multiple Sclerosis, and some choose to use social media.  They share their experiences, and they allow us to see their vulnerability for the betterment of all. Social media can be cold and hurtful, yet it can bring us community and kinship. It’s an individual decision to participate or avoid it.  It’s scary and risky to put ourselves out there, and we need to support those who are willing to share. 

I’m grateful for individuals living and speaking their truth.  Some have been sharing for decades, and some are just starting. I’m heartened by commenters who support with compassion and scroll past when things don’t speak to them.  I’m inspired by so many who cheerlead and model respectful interactions with exceedingly tough topics. I hope we can hang on to the benefits of social media and lose the hurt it can cause.  We need to protect our vulnerable peers, and I hope we can do this with compassion.  We are better for the myriad of voices and experiences. Suffering alone is misery.  Knowing we aren’t alone helps us get through the tough stuff.

It’s tough with any community where individuals are going through a lot personally.  Some people deal with it by lashing out or blaming.  It can be hurtful even when unintentional. I can give lots of examples I’ve experienced and seen, but I’ll share one of my earlier experiences that I think shows how people who understand MS can feel anger toward people who are doing their best. 

Years ago, I agreed to be interviewed for the local newspaper.  The article focused on how I have MS, am open with my health and was doing well professionally. The headline said I wasn’t going to let MS stop me. A comment on the article said I was doing a disservice to all people in the MS Community. She explained her husband had MS and continued working long after he should have left the workforce. It caused her a lot of stress and frustration, because he wasn’t accepting his limitations.  That comment stung.  I hadn’t written the story. I was interviewed, the reporter interpreted what I said, and they presented it in a way that was intended to be complimentary.  I don’t fault them for that.  That said, I didn’t say MS wouldn’t stop me, and it took much more time and brain space than I’d like to admit to accept her comment wasn’t about me. I felt compassion for her situation, but it hurt having her anger directed at me.

At some point the newspaper removed the comment.  I’m not sure if it was a broad-brush removal of comments on old stories or specific to this comment, but I appreciate that it isn’t there anymore.

This experience helped me to shift how I look at social media interactions. When receiving comments, I consider the following:

  • Are they disruptors pushing an agenda or are they genuinely trying to learn?
  • Can I show compassion for them while maintaining my own wellbeing?
  • What can I learn from them?
  • Is the comment about me or them?
  • Does the comment warrant a response?
  • Sometimes a lack of a response is more effective than engaging.
  • Remember comments can be deleted on some platforms.

When commenting on other people’s posts, I consider these questions and perspectives:

  • Does it apply to me?  Do I have anything useful to provide?
  • Why do I feel compelled to react or comment? Am I being supportive?
  • Is my response about me or about their experience?
  • Am I staying on point for what they posted, and is it helpful?
  • Remember each person has a different experience, and what’s true for one is not true for all. 

We all learn different lessons at different times. Things I needed to learn when I was newly diagnosed differ from what I need to learn today and what I’ll need to learn in the coming years.  I see newly diagnosed people expressing where they are in their health journey, and I try to meet them where they are.  Usually it’s just listening and validating their experience.

Some comments can be aggressive, cruel and scary. Others can validate and lift us up. The more we engage respectfully and compassionately, the less scary the internet may become. Cultivating kinship and community helps us individually and collectively. The MS Community is 2.8 million people, and the number of people who care for or about us is exponentially larger. We can make a difference.

*Stacie Prada was diagnosed with RRMS in 2008 just shy of 38 years old.  Her blog, “Keep Doing What You’re Doing” is a compilation of inspiration, exploration, and practical tips for living with Multiple Sclerosis while living a full, productive, and healthy life with a positive perspective. It includes musings on things that help her adapt, cope and rejoice in this adventure on earth. Please visit her at http://stacieprada.blogspot.com/ 

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About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

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