Posts tagged ‘empowerment’

August 3rd, 2011

First Health Activist Chat Recap: Empowerment!

by Amanda

Last Friday we hosted the very first Health Activist Twitter Chat (#HAchat) and it was a great success! Our topic of the chat was “empowerment” and we heard incredible feedback from our participants! We met some new Health Activists and were so glad to have them weigh-in on a topic our community cares so much about. One of our questions was “Are you over it? Is “empowerment” all talk?” and we learned, from your enthusiasm that this whole empowerment thing is just beginning! Thanks to everyone who joined us and look out for our next #HAchat later this month.

Our Topics were:

  1. “Empowerment” is a word thrown around often. What does “being empowered” mean to YOU?
  2. Topic 2: HOW do you empower yourself?
  3. Topic 3: How do you empower OTHERS?
     

    • What if someone isn’t ready to be empowered? How do you help?
  4. Topic 4: How do we take empowerment to the next level?
     

    • Are you over it? Is “empowerment” all talk?

Read on to check out the collected tweets (wisdom, really) from the amazing Health Activists participants…

read more »

July 28th, 2011

Interviewing Health Activists: Annie Martin on Empowerment

by Amanda

 

 

Today we have an empowerment-themed interview with wonderful Health Activist Annie Martin. Annie blogs over at Fragile Annie, where she focuses on moving past chronic illness into living well or, as her blog states boldly: “It’s Time To Get Over How Fragile You Are.” Her blog affirms this positive stance and it was a great experience to hear her take on our theme of empowerment and how she works to empower herself and those around her. Thanks so much for sharing with us, Annie! –Amanda

 

WEGO Health: How has the idea or goal of empowerment inspired you as a Health Activist?

Annie: When I first started my blogging journey, I was frustrated and needed to vent to someone who wasn’t in my direct family!  I had already been sick for about 10 years, and had been treated horribly by so many doctors who stated that this illness was all in my head.  I had no idea that I was going to find a massive family of fellow Fibromyalgia and ME/CFS sufferers along the way.

I felt like no one could understand me on Prince Edward Island, so I turned to the Internet instead.    People I know would listen and learn to be gentle with me (and others suffering from illness). I figured, if nothing else, I can put a face to these illnesses.As the blog grew, I collected more and more diagnoses, and expanded to being a health activist through the blog and through twitter.  Both keep growing every day, as I find more and more people who live like I do and need the support.

WEGO Health: How have you empowered yourself through your Health Activism?

Annie: Before I started being a health activist, I was incredibly hard on myself.  As I couldn’t relate to anyone, I blamed myself for everything that was happening to me.  Blogging about health made me realize that just because I am afflicted with something terrible does not mean I am any less of a person.  It gave me a goal, and became my pride and joy.  I would receive emails saying that a blog entry of mine changed someone’s life entirely, or saved them.  Those messages just made me strive to empower myself and others even more. People with illnesses may not be able to do everything that everyone else can, but we have a set of skills that are still very important and need to be embraced and loved.

WEGO Health: What does “being empowered” mean to you?

Annie: Being empowered, to me, means embracing what you have to work with and running with it.  I knew I felt empowered when I finally felt no shame toward my illnesses.  I could scream it from a rooftop and it wouldn’t bother me in the slightest.  My name is Annie Martin and I have Fibromyalgia, ME/CFS, Gastroparesis, PCOS, Asthma, and High Functioning Asperger’s. Do they cause me problems?  A million!  But do I let them rule my life?  Definitely not!  I know the abuse that people go through in the medical field when they have something that isn’t easily diagnosed.  I want to do every single thing I can to make sure that stops happening.  No one should have to live their life like that, and have their power stolen from them.

WEGO Health: How can others help empower those around them?

Annie: Be HONEST.  Honesty is how we connect with other people.  Everything that I used to keep bottled up, which I’ve since shared, is what draws people to me.  Everyone says – oh I totally have that too and didn’t know anyone else did!  After that, they feel less alone in the world.  Also, in order to help empower people, you have to genuinely care for others.  You have to want to give them your shoulder during the trying times.  You’ll be surprised at the support you get during your hard moments as a result.

WEGO Health: What tips do you have for others who want to share their story and impact others?

Annie: Work with whatever media style fits your personality.  People can write books, write blogs, Twitter information, update statuses on Facebook, and talk to radio or television.  It is crucial right now to get your voice out there.  So many illnesses have mediocre treatments and no cures.  We need to put faces to these illnesses in the hopes of achieving greater research.  It’s integral to our survival.  I really call to the readers of this blog to take a stand and get their voices heard.

A special thanks to Annie for taking the time to share with us – we can’t wait to see where your empowerment continues to take you and your community!

Be sure to check out Annie’s blog Fragile Annie and follow her on Twitter @fragileannie.

 

July 19th, 2011

Standing Up For Yourself Against Misconceptions and Stigma

by Amanda

Today’s post delves into an important topic with regards to our theme of Empowerment – standing up for yourself. Growing up we receive mixed messages about what it means to stand up for ourselves, when to do it, and how to go about it. Sometimes we’re told to turn the other cheek, ignore things that bother us, and avoid situations where we feel uncomfortable. Other times we’re expected to raise our hands, speak up, and protect ourselves and others. It can be a confusing lesson to learn but one that, over time, becomes essential to living well. The balance between advocating for ourselves and speaking up can be difficult to manage especially when so many feelings (anger, frustration, hurt, and more) come right along with it. Health Activists act as an excellent example for not only confronting tough issues like misconceptions and stigma personally but also offer guidance to others who are going through the same thing. Check out Tayla’s great post for more on this. –Amanda

Standing Up for Yourself Against Misconceptions and Stigma

by Tayla Holman

 

As part of this month’s discussion about empowerment, one of the things we want to talk about is how to stand up for yourself against stigma and misconceptions. Keep in mind, however, that standing up for yourself does not mean that you have to knock others down. You can be assertive without being hurtful.

 

Before we can talk about how to stand up against stigma, though, we have to define it. There are two definitions that we can use:

 

1)     A mark of disgrace or infamy.

2)     A mental or physical mark that is characteristic of a defect or disease.

 

For “visible” illnesses or conditions, like psoriasis, a chronic autoimmune disease that appears on the skin, for example – the related stigma often satisfies both of these definitions. People with psoriasis may get the blotches or lesions in highly visible places like their hands, necks, or faces. As a result, they are often treated differently, “like lepers” as some in the community have attested, by people who do not understand the disease. This is a familiar story for anyone who has dealt with a misunderstood health condition. Being treated differently is something many of us, regardless of health condition, go through. No matter the definition, there are ways to confront the stigma. Here are some tips that may be helpful to share with your community.

 

Educate others. – With a visible condition like psoriasis or even invisible illnesses that sometimes entail physical manifestations, encountering public stigma may be inevitable, especially if it covers a large or visible area of your body or affects your stature. If someone makes a comment, or asks you about your condition, explain to them that it is not contagious. Tell them that you are receiving treatment, and that they will not “catch” psoriasis from being around you. Remember that people who judge may simply be afraid or nervous. People are afraid of what they don’t understand, so helping them to understand better will help assuage some of their fears and correct prejudice or misconceptions. As with most things: practice makes perfect. The more you put yourself out there and educate others, the more comfortable you will be and the better you will feel about doing it.

Educate yourself. – Just as important as educating others is educating yourself. Understanding your symptoms, as well as what works and what doesn’t work, helps you empower yourself. Becoming an expert on the condition, especially as it relates to you, puts you in a better position to stand up for yourself when you are approached with misconceptions.

Don’t keep it a secret. – First, reach out to family and close friends. Look for organizations or support groups. If you need to, find a therapist that has worked with other people with your disease or condition.  If you don’t already, you may want to blog about your experiences. Think of how many other people are probably struggling with the same issues, and how your words and advice could help them. Reach out to others who write about it, too. Rely on those you connect with online – they will understand elements of your condition that your friends and family may not relate to. Work together to raise awareness.

Change your attitude. – This is probably the hardest thing to do when it comes to coping with stigma, but it is just as important as the other tips. Since stress can make chronic conditions worse, having a positive attitude can help keep things under control. When it comes to being confronted by others, do not get angry. Offer an explanation if you can. If you can’t, simply walk away. Again, the more you practice being positive and finding solace in your strengths – the more effective it will be. And, when you don’t feel like being positive – reach out to someone who you can vent with or talk to. Take the time to feel your feelings, then work through them as best you can. Taking your mind off of negative things with things and people you love is always a good bet.

 

These are just a few tips that I’ve found from my research – I’m interested in hearing what you’ve tried in your community. What other tips do you have for standing up against misconceptions and stigmas? How do you empower your community to stand up for themselves?

 

July 8th, 2011

First Friday: July Post Prompts

by Amanda

We’re focusing on empowerment this month and what it means to support yourself as a person and as a leader. In supporting yourself and grounding yourself, you will lead your community by example. In line with our theme, our post prompts will center around standing up for yourself and modeling empowerment for others. It is my hope that these prompts will inspire you and, by utilizing them, remind you how great you are and how important you Health Activist work is.

So, if you’re searching for something to write about, post about, or just think about this month – here are some prompts for you. Just come back here, borrow one, and customize if you’d like.

 

  1. Think back to a time you felt truly connected, present, and secure in yourself. Where are you? What are your surroundings? How did you get here? Why do you feel this way? And, if you’d like to bring it back to the present – how can you bring yourself that feeling again?

  2. Stigma plays a huge role in misunderstanding health conditions and can threaten our own well-being and make our missions as Health Activists harder. What stigma is at the top of your list to correct? What would you tell a community member who asked your advice on addressing this stigma in their own life?

  3. It’s easy to compliment others, but harder to compliment yourself. Write down three qualities you have that makes you feel unique, special, and strong.

  4. For some reason, we find ourselves apologizing for expressing ourselves sometimes. When was the last time you said “I’m sorry” for something that you didn’t need to be sorry for? Part of being empowered means having conviction and being ready to stand by your beliefs. Share 5 things that you will not apologize for and reaffirm your commitment to them.

  5. Elaborate upon this month’s FTT – write about what it means to be “empowered” and how you define not only the word but the spirit it evokes. “To me, empowered means ___”

 

As always – if you get inspired and bring one of these prompts to your community, share a link so we can see where you went with it and help share your work!

 

 

July 5th, 2011

Empowering Your Community and Yourself

by Amanda

Photo credit: ElvertBarnes on Flickr

For the month of July we’re going to focus on the emotional aspects of being a Health Activist and the strength, positivity, and tough stuff that comes with being an empowered patient, leader, and, well, person. The recipe for and definition of success isn’t the same for everyone, but by comparing notes – we can find key ways to improve and reinforce our commitment to advocacy and ourselves.

 

This month on the blog, we’ll discuss how to stand up for yourself as a patient or caregiver and how to translate that into standing up for your community. We’ll look into ways that people have rallied for their condition and gotten attention for their causes. We’ll see how people have combated stigma and share tips for starting conversations about stigma. In looking at our emotional empowerment, we’ll see how to utilize each of our online social networks to best take advantage of the resources and community there, while sharing how mindfulness and how disconnecting and getting “off the grid” can be managed and beneficial to your Health Activist well-being. As summer dances itself into full swing, we will see how making the most of opportunities to excel and grabbing precious vacation time are both important parts of being Health Activists. It’s not always easy to feel we’re in the right place with ourselves and our missions, but let’s take this month to emotionally check-in and be good to ourselves.

 

Now, these are probably topics you’ve discussed before and, if so – we hope you’ll share your ideas and posts with us so we can highlight what does and doesn’t work in the challenging world that is Health Activism. I’m looking forward to learning from all of you and helping to collect great tips and tricks for emotional health and self-empowerment – two things that are easy to put on the back-burner when we focus so much on others. Let’s take the time this month to share how we stay real and committed when it’s not easy and make sure we’re keeping self-empowerment as part of our Health Activist equations.