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| Magyar Dermatológiai Társulat |
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| SAM Digital 2021 |
 Rendezvény kezdete: 2021.03.11. | Rendezvény vége: 2021.03.12. |
| Helyszín: online, |
| A rendezvény Web oldala: https://www.eaaci.org/focused-meetings/sam-digital-2021 |
The EAACI-ESCD Skin Allergy Meeting is the leading European meeting in 2021 devoted to skin allergy. The sixth edition of this biennial event will be a digital event taking place on 12 – 13 March 2021 and you can now register!
SAM will be held in collaboration with the European Society for Contact Dermatitis (ESCD). The meeting provides up-to-date information for clinicians, covering basic, translational and clinical aspects on atopic dermatitis, allergic contact dermatitis, mast cell driven diseases, cutaneous drug allergy, anaphylaxis, food allergy and the skin, hand eczema and occupational eczema, among others. We will welcome acclaimed experts presenting keynote lectures.
Moreover, to enhance the learning experience, the meeting will be a platform for interactive discussions and case reports.
We are looking forward to joining you at the first SAM Digital 2021! |
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| Magyar Dermatológiai Társulat |
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| GlobalSkin and ILDS Webinar - Creating the Rare Disease Movement: The Power of the Patient Community |
| Rendezvény kezdete: 2021.02.25. | Rendezvény vége: 2021.02.25. |
| Helyszín: online, |
| A rendezvény Web oldala: https://globalskin.org/index.php?option=com_civicrm&task=civicrm/event/info&reset=1&id=46 |
GlobalSkin is excited to offer our Members programming as part of Rare Disease Day 2021 by co-hosting a webinar, with the International League of Dermatological Societies (ILDS. We are honored to have Dr. Ségolène Aymé, as our special guest speaker at this event. She is Emeritus Director of Research at the French Medical Research Council (INSERM) and the founder of Orphanet.
In 2008, Dr. Segolene Aymé co-authored a journal article entitled, Empowerment of patients: lessons from the rare diseases community. Reflecting on this essay, Dr. Aymé will speak about the power of patients and patient organizations with regards to the Rare Disease Community. She will share her unique perspective and talk about her important work with Orphanet and Expert centers.
We look forward to your participation in this webinar, as you continue to support your patients in new and innovative ways. |
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