Swimming For Psoriasis Press Conference 28 October 2014.

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Transcription de la présentation:

Swimming For Psoriasis Press Conference 28 October 2014

Welcome Prof. Myrto Trakatelli – Dermatologist Miss Dufourny Dominique – Alderwomen of Ixelles

Prof Erwin Tschachler Presentation of the Campaign

Carle Paul, MD, PhD Dermatology department Paul Sabatier University,Larrey Hospital,Toulouse Treatment of psoriasis in 2014 EADV 2014

Psoriasis affects 2 to 3 % of the population

Psoriasis Chronic inflammatory skin disease Non- infectious, non-transmissible Genetic factors Environmental factors : aggressions, bacteria Skin immune system activation and increased skin proliferation and renewal Psoriatic arthritis (15 to 30%)

Psoriasis has a significant impact on quality of life Pruritus, pain, loss of productivity Anxiety and depression Reduced self-esteem, loss of confidence Stigmatisation

Psoriasis does not only affect the skin ! Increased risk of: High blood lipids Diabetes Hypertension Cardiovascular diseases 1. Prey S et al. JEADV 2010;24(Suppl. 2):23– Armstrong AW et al. Br J Dermatol 2013

Treatments of psoriasis s Increased disease severity Oral drugs Methotrexate Ciclosporin Acitretin Injectable Biologicals Anti-TNF Anti-IL-12/23 Topicals : creams Ointments, gels Phototherapy Treatment paradigm is driven by disease severity and burden to patients The different disease severities can be successfully treated Treatment selection is a shared decision by patient and physician

Conclusion – Q&A Start relay

Somes testimonials Politician, Vip’s, Patient Associations

Politician - Miss De Cloedt "De toutes les maladies, l'ignorance est la plus contagieuse. C'est donc elle qu'il faut combattre."

VIP - Thomas Gunzig "Quand j'étais ado, j'avais des boutons partout. Des gros, des rouges, des blancs. Je crois que si quelqu'un avait pris la peine de nager pour me soutenir, ça m'aurait peut être aidé"

VIP - Ben Heine ‘’Vaak wordt gedacht dat psoriasis besmettelijk is maar dat is niet waar. Ik denk dat dit evenement zal het grote publiek tonen dat we kunnen zonder probleem zwemmen met mensen die psoriasis hebben. Het is een heel belangrijk doel en ik ben gelukkig om deel te nemen aan deze nationale sensibiliseringactie.’’

VIP - Vandecaveye Gella “Psoriasis mag geen belemmering zijn om te sporten ondanks de ongemakken en het nakijken. Ik wil heel graag meehelpen om het taboe rond deze huidziekte te doorbreken door samen met “psoriasis patiënten” te zwemmen.”

VIP - Virginie Claes ‘’1) never judge a book by its cover 2) Beauty starts in your head. Not in your Mirror 3) La vie, ce n’est pas d’attendre que les orages passent, c’est d’apprendre comment danser sous la pluie - sénèque’’

VIP - Sophie Nollevaux ‘’Les personnes atteintes de psoriasis doivent savoir qu’elles ne sont pas seules. La solidarité est une valeur très importante pour moi ! Si participer à cette action peut, un tant soit peu, faire changer le fameux « regard des autres », j’aurai bien fait de mouiller le maillot ! ’’

Patients associations – France Psoriasis Today patients wish to be well-informed about treatments options, especially with a condition such as psoriasis. An informed patient is an empowered patient and clearly we still need help and must continue to focus on information and develop even further in our future strategic work. The WHO psoriasis resolution, points out the need for multilateral efforts to promote and improve human health, providing access to treatment and health care education, so this should be definitely a priority. It is a quite common disease which also carries with it an extensive physical, psychological and socioeconomic burden, there are still many gaps in the understanding of the disease itself and its management. Patient’s organisations need support for : Educating the patient about treatment options Educating and supporting patient to better manage their psoriasis in daily life Educating patients about psoriasis as a serious, inflammatory, noncommunicable disease Educating policy makers about psoriasis and its socioeconomic and psychosocial impact Educating the General Public (non communicable disease, non psychological disease)