Hi friends!
Can you believe June is just around the corner? You know what that means – it’s time to get ready for Lipedema Awareness Month! I’ve been planning a new campaign that focuses this year on sharing information outside of our circle, in a BIG, TREMENDOUS, RIDICULOUS way. I can’t wait to share it with you.
I always look forward to this time of year because it gives us a chance to band together and spread the word about this often misunderstood and underdiagnosed condition that impacts so many of us. The more awareness we can raise, the better chance we have of getting proper treatment, support and understanding.
I know living with lipedema can be an uphill battle some days. The pain, swelling, easy bruising and other symptoms are no joke. But you are all such fierce warriors! I’m constantly in awe of your resilience and determination to live your best lives despite the challenges.
That’s why Lipedema Awareness Month is so important. It’s our chance to use our voices and make some noise! When more people understand what lipedema is and how it affects us, it chips away at the stigma and brings us closer to better care and resources.
Here’s the exciting part – there are so many ways YOU can get involved!
Maybe you’re a gifted writer and can pen a powerful blog post or article to educate others. Or perhaps you’re a social media wiz and can spread awareness through eye-catching posts and videos. You could even make and sell lipedema awareness merchandise as a fundraiser.
If you’re more of an offline warrior, you can print out informational flyers and factsheets to distribute in your community. Reach out to your local newspaper about doing a story. Or start a lipedema support group if there isn’t one in your area already. Maybe it’s a one time meet and greet in your area – anything goes!
The possibilities are endless because every single one of you has unique talents and skills to offer! I encourage you to tap into whatever creative outlets you have and use them for lipedema advocacy this June.
It doesn’t matter how big or small your efforts are – anything you can do to raise awareness makes a difference. Even just speaking openly about your own experience can help break down barriers.
So let’s get ready to make some noise, lipedema warriors! I’ll be right there with you, cheering you on every step of the way. Together, we’ve got this!
Wishing you all a wonderful Lipedema Awareness Month filled with impactful advocacy and, as always, unwavering strength.
Stay tuned here and on all my socials. Watch for my hashtags: #LipedemaAwareness #LegsLikeMine and feel free to tag ME in your posts!
Good luck and I can’t wait to see what everyone does!
Susan
