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SUMMARY:International Albinism Awareness Day
DTSTAMP:20221224T172438Z
SEQUENCE:0
UID:309-7-014e54df8e55db0ddedbc25b476240ab@moraga.se
ORGANIZER;CN="Julio Moraga":julio@moraga.se
DESCRIPTION:\n	(A/RES/69/170)\n\n\n\n	Albinism is a rare\, non-contagiou
	s\, genetically inherited difference present at birth. In almost all types
	 of albinism\, both parents must carry the gene for it to be passed on\, e
	ven if they do not have albinism themselves. The condition is found in bot
	h sexes regardless of ethnicity and in all countries of the world. Albinis
	m results in a lack of pigmentation (melanin) in the hair\, skin and eyes\
	, causing vulnerability to the sun and bright light. As a result\, almost 
	all people with albinism are visually impaired and are prone to developing
	 skin cancer. There is no cure for the absence of melanin that is central 
	to albinism.\n\n\n\n	While numbers vary\, it is estimated that in North Am
	erica and Europe 1 in every 17\,000 to 20\,000 people have some form of al
	binism. The condition is much more prevalent in sub-Saharan Africa\, with 
	estimates of 1 in 1\,400 people being affected in Tanzania and prevalence 
	as high as 1 in 1\,000 reported for select populations in Zimbabwe and for
	 other specific ethnic groups in Southern Africa.\n\n\n\n	Health challenge
	s of people living with albinism\n\n	The lack of melanin means persons wit
	h albinism are highly vulnerable to developing skin cancer. In some countr
	ies\, a majority of persons with albinism die from skin cancer between 30 
	and 40 years of age. Skin cancer is highly preventable when persons with a
	lbinism enjoy their right to health. This includes access to regular healt
	h checks\, sunscreen\, sunglasses and sun-protective clothing. In a signif
	icant number of countries\, these life-saving means are unavailable or ina
	ccessible to them. Consequently\, in the realm of development measures\, p
	ersons with albinism have been and are among those “left furthest behi
	nd.” Therefore\, they ought to be targeted for human rights intervention
	s in the manner envisioned by the Sustainable Development Goals.\n\n\n\n	D
	ue to a lack of melanin in the skin and eyes\, persons with albinism often
	 have permanent visual impairment. They also face discrimination due to th
	eir skin colour\; as such\, they are often subject to multiple and interse
	cting discrimination on the grounds of both disability and colour.\n\n\n\n
		People with albinism and human rights\n\n\n\n	People with albinism face m
	ultiple forms of discrimination worldwide. Albinism is still profoundly mi
	sunderstood\, socially and medically. The physical appearance of persons w
	ith albinism is often the object of erroneous beliefs and myths influenced
	 by superstition\, which foster their marginalization and social exclusion
	. This leads to various forms of stigma and discrimination.\n\n\n\n	In som
	e communities\, erroneous beliefs and myths\, heavily influenced by supers
	tition\, put the security and lives of persons with albinism at constant r
	isk. These beliefs and myths are centuries old and are present in cultural
	 attitudes and practices around the world.\n\n\n\n	United Nations Independ
	ent Expert on the enjoyment of human rights by persons with albinism\n\n	T
	he United Nations Human Rights Council adopted a resolution in 2013 (A/HRC
	/RES/23/13) calling for the prevention of attacks and discrimination again
	st persons with albinism. Moreover\, in response to the call from civil so
	ciety organizations advocating to consider persons with albinism as a spec
	ific group with particular needs that require special attention\, the Coun
	cil created the mandate of the Independent Expert on the enjoyment of huma
	n rights by persons with albinism. In June 2015\, the Human Rights Council
	 appointed Ms. Ikponwosa Ero as the first Independent Expert on the enjoym
	ent of human rights by persons with albinism. In August 2021\, she was suc
	ceeded by Ms. Muluka-Anne Miti-Drummond.\n\n\n\n	Violence and discriminati
	on against persons with albinism\n\n	While it has been reported that perso
	ns with albinism globally face discrimination and stigma\, information on 
	cases of physical attacks against persons with albinism is mainly availabl
	e from countries in Africa.  \n\n\n\n	Persons with albinism face more sev
	ere forms of discrimination and violence in those regions\, where the majo
	rity of the general population are relatively dark-skinned. In other words
	\, a greater degree of contrast in pigmentation often gives rise to a grea
	ter degree of discrimination. That appears to be the case in some sub-Saha
	ran African countries where albinism is shrouded in myth and dangerous and
	 erroneous beliefs. The figures on violations against persons with albinis
	m are telling. There have been hundreds of cases of attacks and killings o
	f persons with albinism reported in 28 countries in Sub-Saharan Africa in 
	the past decade. The attacks have several root causes including ignorance\
	, longstanding stigma\, poverty and most abhorrently\, harmful practices e
	manating from manifestation of beliefs in witchcraft. The alarming reality
	 is that these horrendous practices continue today.\n\n\n\n	The manner in 
	which discrimination faced by persons with albinism manifests itself\, and
	 its severity\, vary from region to region. In the western world\, includi
	ng North America\, Europe and Australia\, discrimination often consists of
	 name-calling\, persistent teasing and bullying of children with albinism.
	 Little information is available from other regions such as Asia\, South A
	merica and the Pacific etc. However\, some reports indicate that in China 
	and other Asian countries\, children with albinism face abandonment and re
	jection by their families.\n\n
DTSTART;VALUE=DATE:20140613
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