I read in the self-help groups, on the pages of the various lipedema bloggers and one thing catches my eye again and again.
Envy, resentment, even hateful comments.
But why? Aren't we all in the same boat? Shouldn't it be a platform where we can talk openly? Can you let off the stink? Without being directly attacked?
Don't get me wrong, constructive criticism is great - but please only if an opinion is asked.
Would you say that in real life too?
It's really frightening how easy it is for some people to get really mean things. The Social network has unfortunately lost the barrier to treat each other with respect. Would these ladies also say on the street
“It's your own fault that your lipedema has become so severe. You also have to exercise enough and not just sit on the sofa with chips! "
Seriously people? It's just plain unfair. It is not true. Each of us has our story and only through a small post you don't know the woman behind it. Why did it get so bad, what happened in your past? Can you help her find a better way? But mean comments do not help at all.
We can do better - less envy, more respect
I would like more respect, more understanding from within our own ranks. Who should we expect respect from, if not from us, when we know exactly what life with lipedema feels like.
Since I myself successfully operated I was also approached very meanly. From women who have been robbed of all decency and understanding by lipedema. Yes, it is terrible that the health system is failing us so much that we do not receive adequate support with this disease. I am very sorry that only a few women can afford the operations and many cannot. But believe me when I say that none of the women operated on pays this insane sum out of the postage. We too do without any luxury for a long period of time or - even if it is very difficult - we accept help from friends or acquaintances, or even a loan.
It hurts that one is not granted this new life. You almost feel bad that you have the chance to start over. But that's not how it should be. Nevertheless, we always remain chronically ill and will probably always bear the burden of lipedema on our shoulders.
Thank you for letting me share my thoughts with you ... spray love and respect!