Rare diseases are considered rare, as it afflicts a small number of people in any population; according to the WHO it is less than one per thousand. Therefore, it hardly gets enough attention from governments or from the people in the medical world.
My collaboration with IIT BHU on the #RARE_IS_STRONG campaign also built awareness of India’s national policy on rare diseases. In this discussion, I analyzed the significant provisions of the policy its effectiveness, and its shortcomings.
As part of my efforts to spread awareness about rare diseases, I started a Change.org petition which also requested empowered authorities to help the community of people suffering such diseases. This petition received a boost from IIT BHU.
In coming to terms with my rare health condition, I learnt the importance of keeping my emotions balanced, and the difference acceptance can make to life.
I have tried to convey my journey of the past several years in my writings, the latest of which is a song of acceptance and acknowledgment, but also fear and longing.
Laughter therapy is one of the many alternative therapies I tried to overcome my rare health condition. My experience with it taught me that it is easier to succeed with a smile than fall flat.
The treatment I was undergoing for my rare health condition at times made me feel like I was crawling on broken glass. I focused on searching for a more enduring approach to healing.
In June 2020, I travelled by road from Tamil Nadu to UP with someone who did not share a single language with me. The challenging journey brought me home laden with new learnings, such as the fact that interpretation often matters more than understanding.
My search for alternative, drug-free therapies led me to take up table tennis again, as sports therapy. In the process, I re-educated myself about my health condition.
While battling the health condition, my career took a hit and I also had to face indignity when I tried to revive my career and wondered how companies and offices can become more welcoming for people suffering from rare diseases.
What does it mean to be diagnosed with Isaacs’ Syndrome? What kind of treatment do you seek? What challenges does it throw into your family life? This article about my experience with Isaacs offers some answers.
Rare diseases are considered rare, as it afflicts a small number of people in any population; according to the WHO it is less than one per thousand. Therefore, it hardly gets enough attention from governments or from the people in the medical world.
My collaboration with IIT BHU on the #RARE_IS_STRONG campaign also built awareness of India’s national policy on rare diseases. In this discussion, I analyzed the significant provisions of the policy its effectiveness, and its shortcomings.
As part of my efforts to spread awareness about rare diseases, I started a Change.org petition which also requested empowered authorities to help the community of people suffering such diseases. This petition received a boost from IIT BHU.
In coming to terms with my rare health condition, I learnt the importance of keeping my emotions balanced, and the difference acceptance can make to life.
I have tried to convey my journey of the past several years in my writings, the latest of which is a song of acceptance and acknowledgment, but also fear and longing.
Laughter therapy is one of the many alternative therapies I tried to overcome my rare health condition. My experience with it taught me that it is easier to succeed with a smile than fall flat.
The treatment I was undergoing for my rare health condition at times made me feel like I was crawling on broken glass. I focused on searching for a more enduring approach to healing.
In June 2020, I travelled by road from Tamil Nadu to UP with someone who did not share a single language with me. The challenging journey brought me home laden with new learnings, such as the fact that interpretation often matters more than understanding.
My search for alternative, drug-free therapies led me to take up table tennis again, as sports therapy. In the process, I re-educated myself about my health condition.
While battling the health condition, my career took a hit and I also had to face indignity when I tried to revive my career and wondered how companies and offices can become more welcoming for people suffering from rare diseases.
What does it mean to be diagnosed with Isaacs’ Syndrome? What kind of treatment do you seek? What challenges does it throw into your family life? This article about my experience with Isaacs offers some answers.