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She obtained a merit scholarship at the Romano
Rancilio school in Villastanza of Parabiago. Subsequently, she embarked on a path to scientific high school because her wish was to become a doctor, a wish which did not come true due to her mother's serious health problems which forced her to enter the
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She is a speaker at RAINBOW DIVERSAMENTE RADIO to bring to light the difficulties of people with disabilities in dealing with entertainment or leisure events in general and, of course, Invisible
Disability, with her weekly radio show “Le disabilità Invisibili”.
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With APMARR, for which she is national councilor, she has participated in various projects, such as "Passione Accesa", "good to eat" and has held some lessons on the subject of invisible disabilities in some schools of her Region.
395:. The original draft creator came back and tried to edit it, but does not seem to read their talk page or doesn't understand how the draft process works. I have taken their edit as a request to restore per
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From an early age she had to deal with pain, which however did not prevent her from practicing numerous sports: volleyball, basketball, athletics and above all rhythmic gymnastics, sponsored by REDE of
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With the Luca
Coscioni Association she participated in the collection of signatures as a promoter in her area for the Legal Euthanasia Referendum and in some conferences on Invisible Disabilities.
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tags using the button below. This will let reviewers know a new draft has been submitted in their area of interest. For instance, if you wrote about a female astronomer, you would want to add the
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She loves cooking, even though illness often prevents her from doing so. She has 3 cats, she loves animals, to travel because she want to learn about cultures that are different from her own.
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It has done its utmost to collaborate with the institutions to resolve the particular situations that people with disabilities face regarding the difficulty for disabled stalls.
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Around the age of twenty, the health problems worsened and Pamela had to face numerous visits to get a diagnosis, which never officially arrived.
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The origins of the parents are from Puglia and
Basilicata, of which she is very proud and maintains the traditions, especially culinary.
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fights for the
Sunflower Lanyard to enter the culture of citizenship to make visible disabilities that are not visible at first sight.
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For about 10 years Pamela De Rosa actively participated in the political life of the city of
Parabiago, first in the
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from experienced editors. These venues are only for help with editing and the submission process, not to get reviews.
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Milan srl as an employee. She is very satisfied with her working life and the sensitivity that the company has for
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She is a volunteer at APMARR, NATIONAL ASSOCIATION OF PEOPLE WITH RHEUMATOLOGICAL AND RARE DISEASES and at the
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when addressing this issue). If no additional references exist, the subject is not suitable for
Knowledge.
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PENSALIBERO https://www.pensalibero.it/donne-e-politica-la-parita%E2%80%99-non-sia-solo-numerica/?amp
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https://www.pubblicanow.it/2023/03/21/pamela-de-rosa-cavaliere-al-mertio-della-repubblica-italiana/
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IL POST https://www.ilpost.it/2023/02/07/disabilita-invisibili-nastro-segnalare/
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IL POST https://www.ilpost.it/2023/02/07/disabilita-invisibili-nastro-segnalare/
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Advocate of rights of disabled in Italy. Order of Merit of the
Italian Republic.
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Pamela De Rosa appeared on a article on “Le disabilità invisibili”, year 2020
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In 2021 she got married in a civil ceremony after four years of relationship.
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Referendum
Eutanasia Legale https://referendum.eutanasialegale.it/lombardia/
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world of work to support the family. She’s extremely proud of her choice.
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In 2018, after numerous tests, she was diagnosed with a form of
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Pamela De Rosa was born healthy but at about 10 months due to a
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He has two sisters: Paola, the eldest and Tania, the youngest.
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APMARR https://www.apmarr.it/chi-siamo/il-team-di-apmarr/
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