[vc_section full_width=”stretch_row” css=”.vc_custom_1585128400841{background-color: #576283 !important;}”][vc_row][vc_column][vc_empty_space][/vc_column][/vc_row][vc_row][vc_column width=”1/3″][/vc_column][vc_column width=”2/3″][vc_empty_space][mk_fancy_title strip_tags=”true” tag_name=”h1″ color=”#ffffff” size=”60″ line_height=”90″ font_weight=”bolder” margin_bottom=”0″ font_family=”none”]Silke Rotter (Austria)[/mk_fancy_title][mk_divider style=”thick_solid” divider_width=”custom_width” custom_width=”70″ align=”left” border_color=”#a1aabe” visibility=”hidden-sm”][mk_fancy_title strip_tags=”true” tag_name=”h5″ color=”#ffffff” size=”16″ font_weight=”400″ margin_bottom=”0″ font_family=”none”]Patient advocate[/mk_fancy_title][/vc_column][/vc_row][vc_row][vc_column][vc_empty_space height=”64px”][/vc_column][/vc_row][/vc_section][vc_section full_width=”stretch_row” css=”.vc_custom_1585137324203{background-color: #ffffff !important;}”][vc_row][vc_column][vc_empty_space][/vc_column][/vc_row][vc_row][vc_column width=”1/3″][vc_wp_custommenu title=”Patient advocates” nav_menu=”275″ el_class=”leftsubmenu”][/vc_column][vc_column width=”2/3″][mk_fancy_title strip_tags=”true” color=”#576283″ size=”24″ font_weight=”bold” margin_top=”20″ margin_bottom=”0″ font_family=”none”]Silke Rotter – Mother of Niklas[/mk_fancy_title][vc_row_inner][vc_column_inner width=”1/2″][vc_column_text disable_pattern=”false” margin_bottom=”10″ css=”.vc_custom_1593678643256{margin-bottom: 0px !important;}”]My name is Silke Rotter and I’m 39 years (2019) old. I received my education in Vienna and have worked since 2000 for the Viennese Government. In 2002 I married Alexander (1979). He works as a truck driver for a global pharmaceutical company.
We have three children; they were born in 2003, 2005 and 2016. Our little son Niklas was born with DCMO (Diffuse Capillary Malformation with Overgrowth).
We are very grateful for the CMTC-global Community.[/vc_column_text][/vc_column_inner][vc_column_inner width=”1/2″][mk_image src=”https://www.cmtc.nl/wp-content/uploads/2023/12/cmtc_jubileum25jaar_12.jpg” image_size=”full”][/vc_column_inner][/vc_row_inner][vc_empty_space][mk_custom_box bg_color=”#576283″][vc_row_inner][vc_column_inner width=”1/2″][vc_empty_space][vc_video link=”https://player.vimeo.com/video/596407314″][/vc_column_inner][vc_column_inner width=”1/2″][mk_fancy_title strip_tags=”true” color=”#ffffff” size=”24″ font_weight=”bold” margin_top=”20″ margin_bottom=”0″ font_family=”none”]Our son Niklas[/mk_fancy_title][mk_fancy_title tag_name=”span” color=”#ffffff” size=”16″ font_family=”none”]When Niklas was born in February 2016, he had large red/purple spots on his right foot, leg, buttocks and lower back. The dermatologist told us the next day that he thought he had seen something like this in a book and that he thought it could be CMTC. But he also immediately admitted that he had no idea and had never seen anything like it.[/mk_fancy_title][mk_button dimension=”flat” size=”large” url=”https://www.cmtc.nl/en/blog/2021/02/07/niklas-rotter-austria/” fullwidth=”true” bg_color=”#fad869″]Read Niklas his story[/mk_button][/vc_column_inner][/vc_row_inner][/mk_custom_box][vc_empty_space][vc_row_inner][vc_column_inner width=”1/3″][vc_video link=”https://player.vimeo.com/video/596407423″][vc_column_text css=”.vc_custom_1634915676456{margin-bottom: 0px !important;}”]
Deutsch
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Español
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Français
[/vc_column_text][/vc_column_inner][/vc_row_inner][vc_empty_space][vc_video link=”https://vimeo.com/757484275″][vc_empty_space][vc_btn title=”Facebook page Austria” shape=”square” color=”primary” link=”url:https%3A%2F%2Fwww.facebook.com%2FCMTCOVM.Austria|target:_blank”][mk_fancy_title strip_tags=”true” color=”#576283″ size=”24″ font_weight=”bold” margin_top=”20″ margin_bottom=”0″ font_family=”none”]Want to know more or have any questions?[/mk_fancy_title][vc_raw_html]JTVCY29udGFjdC1mb3JtLTclMjBpZCUzRCUyMjExODAzJTIyJTIwdGl0bGUlM0QlMjJQYXRpJUMzJUFCbnQlMjBiZWxhbmdlbmJlaGFydGlnaW5nJTIwLSUyME9vc3RlbnJpamslMjBFTiUyMiU1RA==[/vc_raw_html][vc_empty_space][mk_custom_box bg_color=”#fad869″][mk_fancy_title strip_tags=”true” color=”#576283″ size=”24″ font_weight=”bold” margin_top=”20″ margin_bottom=”0″ font_family=”none”]Support CMTC-OVM and children like Niklas[/mk_fancy_title][vc_column_text css=”.vc_custom_1612960492326{margin-bottom: 0px !important;}”]With our community we want to improve the quality of life of people who have vascular malformations. CMTC is a rare condition and therefore we think it is important that everyone who has CMTC, or other blood vessel abnormalities, can come into contact with each other. We cannot do this without the support of our donors.[/vc_column_text][vc_row_inner][vc_column_inner width=”1/2″][mk_button dimension=”flat” size=”large” url=”https://www.cmtc.nl/en/members/registration/one-time-donation/” fullwidth=”true” bg_color=”#576283″]Become a donor[/mk_button][/vc_column_inner][vc_column_inner width=”1/2″][mk_button dimension=”outline” size=”large” url=”https://www.cmtc.nl/en/members/registration/membership-registration/” fullwidth=”true” outline_skin=”light”]Become a member[/mk_button][/vc_column_inner][/vc_row_inner][/mk_custom_box][/vc_column][/vc_row][/vc_section][vc_row][vc_column][/vc_column][/vc_row]
