826 comments
I have started a go fund me, no pressure to donate at all. Link is in my bio, I just wanna add that this isn’t covered by any health care-
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Not even private health.. once again please only donate if you can, I really appreciate the love ❤️
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girl start a gofundme. I’d donate a couple of bucks. collectively we can make a difference
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I would feel horrible asking for money for this since it’s classes as a “cosmetic” surgery 😭
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How is this not covered under Medicare? What about health insurance even?
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Neither! How crazy! Not even private health.. can’t believe there are people that can barely walk with this disease and can’t do anything about it
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My mum has lipoedema and I’ve seen how badly it’s affected her - wishing you all the best and thank you for raising awareness!
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Hi love I just donated my last $20 in my spending, but feel free to reply to this comment and remind me and I’ll donate again when I get paid x
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YOUR JOKING! my mum and myself also both have lipodema however ours show up a little differently, mainly in our ankles as fluid gets trapped,
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I’m so excited to see this stage of your journey! You should be so proud of your transformation already! 🥰 Hope it all goes well!
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holy cow on that price!! I hope it all goes well and you're able to get this all under control!! Sending lots of love
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I've just looked! you already have $450 raised and the gofundme has only been up for 2 hours I'm so happy for you! 😅😅😅
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So absolutely blessed, I’m going to be sharing my whole journey to hopefully spread more awareness and get this covered by health care! 🥺
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I’ve left a link in my bio if you’d like to sign to help get this diseased covered by Medicare in Australia 💛
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I went with a cosmetic surgeon and regret it. Love that you mention you’ve chosen a plastic surgeon. Hospital makes recovery way easier. Good luck! ❤️
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Yes I had many followers message to tell me they regret going with a cosmetic surgeon so that’s why I decided to go with a plastic surgeon 😅
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Ur literally the second person I’ve seen in two days say they have this new thing.
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It’s been a thing for a while but no one ever talks about it!! I feel like people are only now starting to spread the word about this disease
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Thank you for sharing your journey! I understand how overwhelming this is. But please document it. You could help so many people.
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Yes! I plan on making it a YouTube series because I can make it more in depth that way!
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is surgery the only way or is there any medication that can help? or is it not researched far enough?
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Hey! I have this too, stage 2 in arms and legs. I had surgery done on my arms recently, I’m literally in debt for it but it was worth it because (1/2)
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