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LIPESE Blog: The thing with lipedema diets
http://blog.lipese.com/2015/07/the-thing-with-lipedema-diets.html
You Are Not Alone. Saturday, July 25, 2015. The thing with lipedema diets. By Tatjana van der Krabben. Recently I read a blog by The Well-Rounded Mama. With a very accessible overview of lipedema symptoms. Something in her introduction resounded with me:. She was referring to websites, but truthfully you see this in support groups as well. We say you can’t diet it off and then talk about diet, recommend diet, compare diets. What is. We are all size-conscious. Is talk of diet wrong? Something used, enjoye...
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LIPESE Blog: May 2015
http://blog.lipese.com/2015_05_01_archive.html
You Are Not Alone. Thursday, May 28, 2015. 75 years of lipedema: treatment depends on your funds. By Tatjana van der Krabben. I could get it through health insurance on grounds of obesity. Wouldn’t we want to prevent. But what if you don’t have the sort of income to make that happen or a nest egg? What if you have been muddling through life with this unrecognized ‘thing’ that got your clothes size to go up and your energy levels to go down? Let’s face it: liposuction doesn’t cure lipedema, bu...Christina...
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LIPESE Blog: March 2015
http://blog.lipese.com/2015_03_01_archive.html
You Are Not Alone. Thursday, March 26, 2015. Dutch lipedema petition just won’t fly. By Tatjana van der Krabben. In December 2014 José Boekelmans, an edema therapist who also has lipedema, started a petition to rally up support to have the costs for liposuction in case of lipedema covered by health insurance in the Netherlands. She had the support of 2 TV personalities, connected to the TV show. You can argue the job was a little big for just one person and not even the TV personalities managed to create...
blog.lipese.com
LIPESE Blog: July 2015
http://blog.lipese.com/2015_07_01_archive.html
You Are Not Alone. Saturday, July 25, 2015. The thing with lipedema diets. By Tatjana van der Krabben. Recently I read a blog by The Well-Rounded Mama. With a very accessible overview of lipedema symptoms. Something in her introduction resounded with me:. She was referring to websites, but truthfully you see this in support groups as well. We say you can’t diet it off and then talk about diet, recommend diet, compare diets. What is. We are all size-conscious. Is talk of diet wrong? Something used, enjoye...
blog.lipese.com
LIPESE Blog: Lipedema film fun
http://blog.lipese.com/2015/06/lipedema-film-fun.html
You Are Not Alone. Monday, June 1, 2015. By Tatjana van der Krabben. First there was a little and then there was a lot: filmed material about lipedema. The most treasured ones are those made by women with lipedema. They made it visible to the world what it is like to have lipedema. They gave lipedema awareness wings on social media. This blog features some of these initiatives. Last year the Dutch also felt they really needed something more visual, in their own language, to share on social media and use ...
blog.lipese.com
LIPESE Blog: Highlights from Dutch Lipedema Day Conference – Part 2
http://blog.lipese.com/2015/06/highlights-from-dutch-lipedema-day_19.html
You Are Not Alone. Friday, June 19, 2015. Highlights from Dutch Lipedema Day Conference – Part 2. By Tatjana van der Krabben. On May 30, 2015 I attended the 5. Dutch Lipedema Day in the lovely southern part of the Netherlands. It’s impossible to cover everything I heard and learned that day. In this blog - part 2 - I will point out some interesting facts and figures I picked up that day. To be continued, then? Interesting detail was that Ms. Smeets-Taubitz referred to women sweating who were ‘n...Ms Smee...
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LIPESE Blog: Lipedema Sister Laura Deese Reaches Out
http://blog.lipese.com/2015/04/lipedema-sister-laura-deese-reaches-out.html
You Are Not Alone. Wednesday, April 1, 2015. Lipedema Sister Laura Deese Reaches Out. Laura Deese, a fellow Lipedema sister, has reached out to lipese.com through our Twitter page. She's also reached out to her local community by sharing her story with Channel 5, WNEM, near her home in Iosco County, MI. You can see the story reported by WNEM here:. WNEM TV 5 Laura Deese. It took Laura 14 years to discover she had lymphedema and she was recently diagnosed with lipedema last November. Laura Deese needs hel...
blog.lipese.com
LIPESE Blog: June 2015
http://blog.lipese.com/2015_06_01_archive.html
You Are Not Alone. Friday, June 19, 2015. Highlights from Dutch Lipedema Day Conference – Part 2. By Tatjana van der Krabben. On May 30, 2015 I attended the 5. Dutch Lipedema Day in the lovely southern part of the Netherlands. It’s impossible to cover everything I heard and learned that day. In this blog - part 2 - I will point out some interesting facts and figures I picked up that day. To be continued, then? Interesting detail was that Ms. Smeets-Taubitz referred to women sweating who were ‘n...Ms Smee...
blog.lipese.com
LIPESE Blog: Highlights from Dutch Lipedema Day Conference – Part 1
http://blog.lipese.com/2015/06/highlights-from-dutch-lipedema-day.html
You Are Not Alone. Monday, June 15, 2015. Highlights from Dutch Lipedema Day Conference – Part 1. By Tatjana van der Krabben. On May 30, 2015 I attended the 5. Dutch Lipedema Day in the lovely southern part of the Netherlands. It’s impossible to cover everything I heard and learned that day. In this blog I will point out some interesting facts and figures I picked up that day. Lipedema is very uncommon in South East Asia. At the same time most cases are reported in the western world. Dr Veraart mentioned...
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