10 Things to take to the Hospital with You

IBDers often are hospital frequent flyers. While I don’t keep a packed bag around, over the years, I have gotten a routine down, and so have my loved ones in case I am not able to pack my bag. Here is what I find essential to take to the hospital- for practical reasons and because I need them for my mental well-being (which is equally important). Update Oct 29: I have included feedback that I got from the members ofRead more

Travelling with IBD- Tips to make the journey smoother I

I haven’t written much, life has been hectic, and, I was visiting my family in ze fatherland. I have been back and forth between Europe and the US since 2004, and I have traveled extensively within the US.  Here are a few things picked up along the way. The Planning phase: Talk to your doctor: No matter how well you may feel, no matter how great your blood work looks like, make sure your doctor is on board (pardon theRead more

What’s in my bag? -Post-op Crohn’s Edition

As a German, you get culturally conditioned to be prepared. We are a people of planners and what-iffers.  This can be debilitating, but it can also be empowering. In my case, it empowered me to leave the house after my surgeries, wound vac or not, trans-rectal drain or not. So, I packed my bag and went. Here are the absolute essentials that I have in that bag. Not everything is Crohn’s-related, but still useful. Sunglasses. Having lived in CA forRead more