SAPL Surgery – the second step!

Update on SAPL surgery …thanks for sharing…

The Lymphosaurus Rex

Hey all,

Gosh its been a while since I did an update on the blog; but not much has happened up until recently. (If you want more regular news from me, its best to follow me on Instagram @lymphosaurs_rex)

I recently went to Paris for “stage two” of my Lymphedema surgery plan and had a liposuction procedure (SAPL) with Dr Becker. The goal was to remove the fibrous tissue (mainly on the exterior side of my left left) that has accumulated over the years of living with LE. To the naked eye, it looks like nothing but a fat leg, but when you touched my leg it was kind of harder in some spots than others.

The procedure took about one hour and I was a day patient at the hospital (no overnight stay required). I never really had a huge amount of pain (stopped taking the pain killers around day…

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8 months post-op

Thanks for sharing your progress with us

The Lymphosaurus Rex

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Hi everyone,

It’s been 2 months since my last blog and lots has happened in between now and then. These last two months have really been an emotional rollercoaster for a variety of reasons. I’ve been very immersed in my own little Lymphedema world, researching, learning more and more (and also being disappointed with the lack of up-to-date information on the internet). I’ve been connecting more and more with others who suffer from this condition, listening to their experiences and stories (2 hour long phone calls to the USA, United Kingdom, Solvenia!), which has been incredible! It always feels like I’m listening to an echo of my own story when I speak with other Lymphies; the similarities are fascinating.

I’ve really had the urge to do something more with my blog, my story, my mission to raise awareness of Lymphedema, which in turn has been pretty draining on me mentally. I feel like there…

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Lymphoedema Awareness Week

Support the awareness campaign in the UK… Wear your odd socks and donate.. Thanks Lauren for this… As always an inspiration 😃😃

LymphFashion Lymphoedema

Hey Beautifuls!

This week in the UK has been Lymphoedema Awareness Week. Lymphoedema gets less press than it deserves. It’s also more common than people realise. There are at least 240,000 sufferers in the UK and around 6 million in the USA. The condition has been ignored by medical professionals for so long. NOW IS THE TIME FOR CHANGE! We will be ignored no longer.

The Lymphoedema Support Network (LSN) are taking a stand! They have started a social media campaign- ‘Sock it to Lymphoedema’. The aim is to donate as much to charity as possible through wearing odd socks for a day and nominating someone else to do the same.

Many of us have already taken part. SO SHOULD YOU! Follow these 3 steps:

1.Take a picture of yourself wearing odd socks, upload it to social media

2. Text 70070  with the code LSNS14 followed by an amount of…

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