

Unless we all come together, there is no global movement to end TSW. Your support matters now, more than ever.
If you or someone you love has had their life upended by TSW, this is your chance to take action and have your voice heard.

Because of the generosity of people like you, Abigel's mom was able to find ITSAN and discover the truth about topical steroids - but countless others are still unaware they are dealing with TSW.

It's not always the size of the donation that matters, it's how it all adds up.

Thanks to our amazing community, ITSAN recently took a massive leap towards better understanding the TSW journey by partnering with The National Organization for Rare Disorders in the development of a TSW patient registry.
With your help, we can:
We aim to provide a safe place for people going through TSW, and those who care for them.
We work tirelessly to build the evidence we need to prove the severity and prevalence of TSW.
We are a voice for all those affected and strive to raise awareness, so TSW becomes recognized globally.