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Misinformation around psoriasis

Community of Psoriasis supporters initiative led by DakshamA Health is organizing a session on 27th of January, 2023, Friday 06:00 PM to 07:00 PM IST. with Dr. Krupa Shankar D.S, Consultant Dermatologist, Mallige Medical Centre, Banglore. Ask your queries live from the expert.

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Psoriasis and COVID-19

Community of Psoriasis supporters initiative led by DakshamA Health is organizing a session on 01st of October, 2022, Saturday 12:00 pm to 01:00 pm IST. with Dr. Vibhu Mendiratta, Dermatologist, Head, Dept of Dermatology, Lady Hardinge Medical College Ask your queries live from the expert.

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UNITING FOR ACTION- BUILDING A VOICE FOR PSORIASIS PATIENTS IN INDIA

On the occasion of World Psoriasis Day, 27th October,2022, Community of Psoriasis Supporters (Initiative by Dakshayani and Amaravati Health and Education) in collaboration with Indian Association of Dermatologists, Venereologists and Leprologists (IADVL) is organizing a virtual event with the theme “Uniting for Action- Building A Voice for Psoriasis Patients in India”, 04:00 PM IST onwards.

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Meditation & Healing session- De-stressing yourself

: Community of Psoriasis supporters initiative led by DakshamA Health is organizing a meditation and healing session on 27th September 2022, Tuesday 04:00 pm to 05:00 pm IST. with Prianca, Yoga and meditation facilitator. We invite psoriasis patients, and caregivers to attend the session. Join our meditation session to release your stress.

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Open House Meeting

Community of Psoriasis supporters initiative led by DakshamA Health is organizing an open house meeting on 17th September 2022, Saturday 12:00 pm to 01:00 pm IST. Let us meet up and discuss about our journey.

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Psoriasis and its co-morbidities

We invite a psoriasis patient and caregivers to join the session Rare Psoriasis Disorder-What you need to know? on 27th of August, 2022, Saturday 03:00 pm to 04:00 pm IST with Dr.Rashmi Kumari, Dermatologist, Prof, and HOD of dermatology, JIPMERDermatologist, Prof, and HOD of dermatology, JIPMER.

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Roadmap for the inclusion of new rare diseases—Discussion on stakeholder responsibilities and accelerated regulatory pathways

The round table discussion deliberated about the roles and responsibilities of the stakeholders involved in the identification, treatment, and inclusion of new rare diseases, as well as explored accelerated regulatory pathways for new rare dermatological disease treatment options.We would like to thank all our experts who have made this discussion insightful and fruitful.

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Psoriasis and its co-morbidities

Community of Psoriasis supporters' initiative led by DakshamA Health is organizing a session on the 16th of July 2022, Saturday 04:00 pm to 05:00 pm IST with Dr. Vishalakshi Viswanath, Prof and Head of Dept. Of Dermatology, Rajiv Gandhi Medical College and CSMH, Kalwa, Thane Municipal Corporation, Maharashtra.

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Open House Metting

Community of Psoriasis supporters' initiative led by DakshamA Health organised an open house meeting with psoriasis supporters and caregivers on the 14th of May 2022, Saturday 12:30 pm to 01:30 pm IST.

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Living with Psoriasis - You are not alone

Community of Psoriasis supporters' initiative led by DakshamA Health organised a session on the 15th of April 2022, Friday 03:00 pm to 04:00 pm IST. To watch the full session, click below

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Rare Disease Policy- scope for inclusion and treatment of New Rare Diseases not included in National Rare Diseases Policy.

On the occasion of World rare disease Day 2022, Dakshayani and Amaravati Health and Education organized a round table discussion to explore opportunities for inclusion of rare diseases not included in the National rare diseases policy and pathways for inclusion and access to treatments. This round table discussion emphasized the need and importance to explore the opportunities and challenges in rare dermatological conditions in India. There are several challenges that make the diagnosis and treatment of rare skin diseases difficult. Limited advanced clinical resources and far-to-reach, sporadically localized service facilities and the high cost of treatments have hampered the services’ reach to patients in low and middle-income countries like India. Disease categorization in the Rare Disease Policy often makes it difficult to categorize some of these diseases into straight-jacketed silos as there are varying stages of the disease. To know more about the event, click on the link below