<\/a><\/li><\/div>
Creation of a national teledermatology service<\/a><\/h4>
Mali, faced with a regional dermatologist shortage, is assessing the feasibility of a telemedicine programme. Objectives: improve healthcare and create a true communications network.<\/p>31\/07\/2018<\/em><\/span><\/div><\/article><\/section><\/div>
<\/div><\/div><\/div>See also<\/span><\/h4>\n<\/div>
Prevention, diagnosis and treatment of sickle cell disease<\/a><\/h4>
Fondation Pierre Fabre supports the Comit\u00e9 d'Initiative contre la Dr\u00e9panocytose (Sickle Cell Disease Initiative Committee) in Burkina to pursue a project of unprecedented scale in the country.<\/p>30\/07\/2018<\/em><\/span><\/div><\/article><\/section><\/div>
<\/div><\/div><\/div>Follow our action<\/span><\/h4>\n<\/div>
![\"\"](\"https:\/\/sandbox.fondationpierrefabre.org\/wp-content\/uploads\/sites\/9\/2019\/09\/FU2I9889-700x441.jpg\")
<\/a><\/li><\/ul><\/div>tma25pf<\/a><\/span><\/span>2019-10-16T11:43:30+02:00<\/span>Fondation Pierre Fabre celebrated 20 years of commitment to healthcare in the Global South<\/a><\/h4>
Fondation Pierre Fabre celebrated 20 years of commitment to healthcare in the Global South 13\/09\/2019 The day brought together more than 300 leading figures from the scientific, medical, academic, humanitarian<\/p><\/div><\/article><\/section><\/div>
Improving management of noma<\/h1>\n\u2014 Burkina Faso \u2014<\/span><\/em><\/h3>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>![](\"https:\/\/sandbox.fondationpierrefabre.org\/wp-content\/uploads\/sites\/9\/2018\/07\/dsc_1283_0.jpg\" "\\"dsc_1283_0\\"")
<\/span><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>BACKGROUND<\/strong><\/span><\/p>\n<\/div>\n<\/div><\/div><\/div>Noma, often associated with extreme poverty, is a gangrenous stomatitis that develops in the mouth and destroys the face\u2019s soft and bone tissues. It is mainly caused by hygiene issues, malnutrition and immune deficiency related to infectious diseases.\u00a0Nearly 100,000 people worldwide are affected by the malady each year, mostly children<\/strong>. Of these, only 20% survive: such deformation means they have trouble eating and breathing.<\/p>\nIn 2000, anxious to put a face to these children, Dr Bellity carried out a first operation in Paris on Fati, a little girl from Burkina Faso. It was a success. However, seeing the separation trauma when time came for the girl to return to her home country, he decided that future operations would take place over there. Les Enfants du Noma (The Children of Noma) was born. This association arranges regular missions at the Maison de Fati, a local support facility for children and their carers. There, a total of 21 surgeons, 10 anaesthesiologists, four doctors and 37 nurses repair the disastrous effects of noma, but also address tumours, cleft lips and orthopaedic problems.\u00a0Since the association was founded, its staff has treated 2,500 children<\/strong>.<\/p>\nIn 2014, Fondation Pierre Fabre, well aware of the issues involved in tropical dermatology, decided to support Les Enfants du Noma.\u00a0It will fund nine missions in Burkina Faso through 2017<\/strong>. It will also create a scholarship and professional development in maxillofacial surgery for local specialists. The fellows will be received in teaching hospitals in Saint-Etienne, Caen and Marseille, and Marseille\u2019s army hospitals. Lastly, the Foundation will provide advocacy support by carrying out information campaigns on noma.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div>KEY FACTS<\/span>
\n<\/strong>_____<\/span><\/p>\nPriority<\/strong><\/span>
\nTropical dermatology<\/span><\/p>\nProgramme<\/strong><\/span>
\nSince 2015<\/span><\/p>\nType of involvement<\/strong><\/span>
\nDistributor and operator<\/span><\/p>\nActions<\/strong><\/span><\/p>\n\n- Scholarship (covering six months in France and on-site training during Les Enfants du Noma interventions)<\/span><\/li>\n
- Supply of academic training textbooks<\/span><\/li>\n
- Organisation of academic training presentations<\/span><\/li>\n
- Funding for 9 annual missions of Les Enfants du Noma (including purchase of medicines and equipment)<\/span><\/li>\n
- Information campaigns<\/span><\/li>\n<\/ul>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>
Enfants du Noma
\nCHU Nord – Service de Chirurgie Maxillo-Faciale
\nPr. Seguin
\n42055 Saint-\u00c9tienne CEDEX 2
\nContact :\u00a0secretariatedn@gmail.com<\/a>
\nhttp:\/\/www.enfantsdunoma.info<\/a><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>![](\"data:image\/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==\")
<\/div><\/div><\/div>![\"\"](\"data:image\/svg+xml,%3Csvg%20xmlns%3D%27http%3A%2F%2Fwww.w3.org%2F2000%2Fsvg%27%20width%3D%2775%27%20height%3D%2763%27%20viewBox%3D%270%200%2075%2063%27%3E%3Crect%20width%3D%2775%27%20height%3D%2763%27%20fill-opacity%3D%220%22%2F%3E%3C%2Fsvg%3E\")
<\/span><\/p>\nNoma is a particularly devastating disease. The repair techniques used to treat its manifestations are sophisticated and often require several operations spaced over a number of months. This surgery cannot take place if there is not highly professional medical oversight. With the help of the Maison de Fati, Les Enfants du Noma has created a facility to receive and treat these children, so that they can benefit from the monitoring and care they need until the repairs are complete.\u201d<\/span><\/p>\nDr Philippe Bellity<\/span><\/strong><\/span>
\nPlastic surgeon, Founder and President of Les Enfants du Noma<\/span><\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div>Future initiatives<\/span><\/h3>\n<\/div>The partnership between Les Enfants du Noma and Fondation Pierre Fabre is expected to expand to encompass treatment of giant keloids, which are skin growths due to abnormal scarring. Furthermore, both parties are considering spreading their work to other countries.<\/p>\n<\/div>
<\/div><\/div><\/div><\/div><\/div>PARTNERS<\/h2>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div>\n- Enfants du Noma<\/a><\/li>\n
- La Maison de Fati<\/a><\/li>\n
- CHU de Saint-Etienne<\/a><\/li>\n<\/ul>\n<\/div><\/div><\/div><\/div>
\n- CHU de Caen<\/a><\/li>\n
- CHU de Marseille<\/a><\/li>\n
- H\u00f4pitaux des arm\u00e9es de Marseille<\/a><\/li>\n<\/ul>\n<\/div><\/div><\/div><\/div><\/div><\/div>
See also<\/span><\/h4>\n<\/div>- <\/a><\/li><\/div>
Creation of a national teledermatology service<\/a><\/h4>Mali, faced with a regional dermatologist shortage, is assessing the feasibility of a telemedicine programme. Objectives: improve healthcare and create a true communications network.<\/p>31\/07\/2018<\/em><\/span><\/div><\/article><\/section><\/div><\/div><\/div><\/div>See also<\/span><\/h4>\n<\/div>
<\/span><\/div><\/div>BACKGROUND<\/strong><\/span><\/p>\n<\/div>\n Noma, often associated with extreme poverty, is a gangrenous stomatitis that develops in the mouth and destroys the face\u2019s soft and bone tissues. It is mainly caused by hygiene issues, malnutrition and immune deficiency related to infectious diseases.\u00a0Nearly 100,000 people worldwide are affected by the malady each year, mostly children<\/strong>. Of these, only 20% survive: such deformation means they have trouble eating and breathing.<\/p>\n In 2000, anxious to put a face to these children, Dr Bellity carried out a first operation in Paris on Fati, a little girl from Burkina Faso. It was a success. However, seeing the separation trauma when time came for the girl to return to her home country, he decided that future operations would take place over there. Les Enfants du Noma (The Children of Noma) was born. This association arranges regular missions at the Maison de Fati, a local support facility for children and their carers. There, a total of 21 surgeons, 10 anaesthesiologists, four doctors and 37 nurses repair the disastrous effects of noma, but also address tumours, cleft lips and orthopaedic problems.\u00a0Since the association was founded, its staff has treated 2,500 children<\/strong>.<\/p>\n In 2014, Fondation Pierre Fabre, well aware of the issues involved in tropical dermatology, decided to support Les Enfants du Noma.\u00a0It will fund nine missions in Burkina Faso through 2017<\/strong>. It will also create a scholarship and professional development in maxillofacial surgery for local specialists. The fellows will be received in teaching hospitals in Saint-Etienne, Caen and Marseille, and Marseille\u2019s army hospitals. Lastly, the Foundation will provide advocacy support by carrying out information campaigns on noma.<\/p>\n<\/div> KEY FACTS<\/span> Priority<\/strong><\/span> Programme<\/strong><\/span> Type of involvement<\/strong><\/span> Actions<\/strong><\/span><\/p>\n Enfants du Noma Noma is a particularly devastating disease. The repair techniques used to treat its manifestations are sophisticated and often require several operations spaced over a number of months. This surgery cannot take place if there is not highly professional medical oversight. With the help of the Maison de Fati, Les Enfants du Noma has created a facility to receive and treat these children, so that they can benefit from the monitoring and care they need until the repairs are complete.\u201d<\/span><\/p>\n Dr Philippe Bellity<\/span><\/strong><\/span> The partnership between Les Enfants du Noma and Fondation Pierre Fabre is expected to expand to encompass treatment of giant keloids, which are skin growths due to abnormal scarring. Furthermore, both parties are considering spreading their work to other countries.<\/p>\n<\/div> Mali, faced with a regional dermatologist shortage, is assessing the feasibility of a telemedicine programme. Objectives: improve healthcare and create a true communications network.<\/p>31\/07\/2018<\/em><\/span><\/div><\/article><\/section><\/div>
\n<\/strong>_____<\/span><\/p>\n
\nTropical dermatology<\/span><\/p>\n
\nSince 2015<\/span><\/p>\n
\nDistributor and operator<\/span><\/p>\n\n
\nCHU Nord – Service de Chirurgie Maxillo-Faciale
\nPr. Seguin
\n42055 Saint-\u00c9tienne CEDEX 2
\nContact :\u00a0secretariatedn@gmail.com<\/a>
\nhttp:\/\/www.enfantsdunoma.info<\/a><\/p>\n<\/div>![\"\"](\"http:\/\/sandbox.fondationpierrefabre.org\/wp-content\/uploads\/sites\/2\/2018\/07\/Sans-titre-1-1.png\")
\nPlastic surgeon, Founder and President of Les Enfants du Noma<\/span><\/p>\n<\/div>Future initiatives<\/span><\/h3>\n<\/div>
PARTNERS<\/h2>\n<\/div>
\n
\n
See also<\/span><\/h4>\n<\/div>
![\"\"](\"https:\/\/sandbox.fondationpierrefabre.org\/wp-content\/uploads\/sites\/9\/2018\/09\/img_0486_1440x710.jpg\")
Creation of a national teledermatology service<\/a><\/h4>
See also<\/span><\/h4>\n<\/div>
![\"\"](\"https:\/\/sandbox.fondationpierrefabre.org\/wp-content\/uploads\/sites\/9\/2018\/09\/proposition_photo_majeure_bg2.jpg\")
<\/a><\/li><\/div>