From our partner Irene Tarragó

2023 has already ended and we begin 2024 with 366 days ahead (this year is a leap year) where we can write the numerous blank pages they represent.

First of all, I want to wish you all a year full of challenges achieved. To people with epilepsy, we wish you to control the disease in the best possible way, that it does not stop you from achieving your dreams; To the family members, that you do not suffer for us more than necessary; that, sometimes, we are more capable of doing things than you think; that you have to let us experiment and fail, because, above all, we are people, children, adolescents, young people or, like me, already grandmothers, who have to have as normal a life as possible, like any other person. Having our own experiences, with successes and failures, like everyone. We are not made of glass. We need your support but, also, that you give us space and freedom.

In my life I have been able to do what I have set out to do. It is true that my medication has controlled me wonderfully; but, it is also true, that I have been constant, that I always took it, that I never drank alcohol, that I organized my life so that I could sleep 8 hours and, at the same time, enjoy friends and activities and, at the same time, I have always I had the unconditional support first of my parents and then of my husband and my children. I have always been truthful, I mean that I have never hidden the fact that I had epilepsy. It’s not that I was always talking about it, but when I arrived at a new place where I was going to be for a while (for example, a new job, a gym…) I would mention it to the person closest to me (my boss or my coach). ) and thus they were informed of what they had to do in case of a crisis. That I have done sports such as swimming, horse riding, basketball, golf… that I have carried out cultural activities such as theater or singing… that I have developed the jobs that I have liked and dedicated my time to politics… Come on, I have done what I have always done. I have proposed. You can do it too. Come on!

I have always been truthful, I mean that I have never hidden the fact that I had epilepsy.

Well, nothing more to say at this beginning of the year. Enjoy life, we don’t know what expiration date we have. Many kisses.

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Save the date

The next Saturday 21st of November at 4 pm, you will be able to know first hand our product: mjn-SERAS.
mjn-SERAS is a healthcare product that sends a warning signal when the risk of epileptic seizures is high, to the affected person and their trusted contacts.

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    mjn-SERAS is a medical device with CE marking according to the European Directive 93/42/EEC and the Royal Decree RD. 1591/2009.
    Contraindications: Do not use the product if you suffer from an infection in the ear canal or if you suffer from a skin lesion in the vicinity of the product's area of influence.
    Considerations: This medical product works with an APP only on Android phones. The results tested are 96% sensitivity and 94% specificity.

    Save the date

    El próximo sábado 21 de noviembre a las 4 de la tarde, podrás conocer de primera mano nuestro producto: mjn-SERAS.
    mjn-SERAS es un producto sanitario que lanza una señal de aviso cuando el riesgo de crisis de epilepsia es elevado, a la persona afectada y a sus contactos de confianza.


      mjn-SERAS es un producto sanitario con marcado CE conforme a la Directiva Europea 93/42/EEC y el Real Decreto RD. 1591/2009.
      Contraindicaciones: No usar el producto en caso de padecer una infección en el canal auditivo o en caso de padecer una lesión cutánea en las proximidades del área de influencia del producto.
      Consideraciones: Este producto sanitario funciona con una APP solo en teléfonos Android. Los resultados testeados son 96% de sensibilidad y 94% de especificidad.