I am Jessica Langenhoff, Human Movement Scientist and biomedical information specialist. Diagnosed chromodiverse as an adult. Mom to a teenage son. My aim is to make biomedical information accessible to as many people as possible. Especially scientific biomedical information to people living with diagnoses. In this way, I try to build a bridge between science and everyday living. Also the reverse can be true: giving scientists and healthcare professionals input for their efforts to help people with diagnoses. Both by retrieval and summarizing of scientific evidence and by voicing what lives within the community of chromodiverse people.
I started XXs2info (access to info) in 2020 as my brand name being self employed. I saw an opportunity to combine communication and information services in one. After two years, I stopped as XXs2info suffered failure to thrive. I look back without regrets: at least I gave it a try and I learned so much from it.
As a volunteer, I am still active, supporting several patient advocacy groups. I am webmaster for the Dutch Contactgroep Triple X-Syndroom, write new texts and translate from English to Dutch, make plain language summaries. Because ging access to information is still a good description, the name XXs2info stayed.