Connecting with the Community: Lymphoedema United Meet-Up
- rachaelboggiano
- Apr 15
- 1 min read
Updated: May 20
Connecting with the Community: Lymphoedema United Meet-Up
As part of my efforts to connect more deeply with the lymphoedema community, I recently attended a community meet-up at St. George's Hospital. It was an informal, welcoming event, complete with tea, biscuits and open conversation. We shared our personal journeys, our biggest challenges and the top tips and tricks we’ve discovered along the way.
The group was diverse in age and background, with a mix of both primary and secondary lymphoedema patients. Despite our different stories and experiences, there was an incredible sense of solidarity in the room. It was so refreshing to speak candidly with people who truly understand the emotional and physical impact this condition can have. I also found it incredibly helpful to hear how others are managing their swelling, whether that was through specific routines, garments or mindsets.
The event was sponsored by Sigvaris Group Britain and a representative from their compression garment team joined us to showcase some of their latest products. A big focus of their presentation was donning and doffing ad how to make the process easier and more accessible for all users, regardless of age or mobility.
I left feeling empowered, supported and much more confident in continuing to share my own journey and strategies. I’ll definitely be attending more events like this in the future. It’s comforting to know there’s a community of people out there who truly get it and who are just as determined to live fully despite the condition.
Links:
Lymphoedema United - https://lymphoedemaunited.com/
Free Membership for Lymphoedema United - https://lymphoedemaunited.com/free-membership/
Lymphoedema United 'You Are NOT Alone!' Meet-Ups - https://lymphoedemaunited.com/whats-the-latest/
