Finding out you have a serious disease can be an isolating time.

But thanks to your heartfelt generosity, Meg’s blood cancer experience has been full of support from people who understand.

Facing uncertainty

In February 2020, Meg’s life changed when she was given an inconclusive diagnosis of either myelodysplastic syndrome (MDS) or aplastic anaemia.

Facing the COVID-19 pandemic and an uncertain diagnosis, the 27-year-old felt alone and vulnerable.

Finding her online community

However, it was your support that ensured Meg could access a community of Australians who knew how she felt.

From the moment she logged on to her first online Leukaemia Foundation support group, Meg felt reassured meeting others who had walked a similar path.

“I get so much out of it. The emotional support and strategies you get are just brilliant,” Meg explains.

“You can’t replicate that feeling of being seen or heard”

Being able to share and learn from others has meant so much to Meg, giving her the chance to feel empowered about all aspects of her blood cancer experience.

“Sometimes I’ll learn about a treatment, or I might just listen to someone who is feeling the same as I am. You can’t replicate that feeling of being seen or heard,” reflects Meg.

No boundaries

The flexibility and welcoming nature of the online groups have given Meg the chance to share from wherever she is and with no filter.

“I’ve even dialed in from my husband’s soccer game! Other participants have joined from their hospital bed,” said Meg.

“They’ve given me space to express exactly how I feel without fear of judgement.”

“I feel more prepared for what’s ahead of me and have learnt so much. This support has meant the world, thank you!”