I was reading the comments left underneath the video of Nicky and I noticed a lot of people are asking the same questions over and over again. But… just not to me, to the “wind”, so to speak. So, I want everyone to know it’s ok to ask me or Nicky questions. In fact, we encourage it. You can either ask it in the comments below this post or you can come on over to his FACEBOOK PAGE and either post your question or send a message to the page. Here’s a description of Epidermolysis Bullosa taken from my book Butterfly Child: “Nicky’s condition is called “Epidermolysis Bullosa”, he has the Recessive Dystrophic form. This is a long fancy name for a condition of the skin where a certain protein called “collagen”, which acts as a glue between the epidermis and the dermis, is missing or the body simply does notRead More →

Hello everyone! Here’s video #2 (Video #1 is here) of our series “Ask Nicky”. My son Nicky was born with the Recessive Dystrophic form of Epidermolysis Bullosa. He is 18 now. In this video his brother Connor (11 years old, EB free) is here as well answering questions. If you have any questions for Nicky about his life with EB please leave a comment below. Don’t assume what his life may be like, just ask! We love questions! Thank you so much for caring about Nicky! Love and Light Post Views: 725Read More →

A big thank you to those that sent their questions to Nicky! Here’s the video as promised. Connor said he feels left out, so please submit more questions for Nicky and some for Connor too for another video coming soon! Thank you so much for your kindness and for caring about Nicky. Let’s kick EB’s butt! Much Love, Post Views: 691Read More →

I will be done with my book real soon, and then comes the hard part of selling it or self-publish it, we’ll see. However, in the new year, I want Nicky himself to be able to answer questions on a video I will make of him which I will then upload to YouTube. So, ASK away by leaving a message below on the facebook plug-in. Please be kind and sensitive, it’s all I ask. Nicky is truly a trooper, he wants everyone to know about his condition, so we’re gonna run with it. I am hoping to make several videos each perhaps tackling a different subject per se depending on what Nicky is comfortable talking about. Remember, Nicky is 18 years old now, and he has the (Hallopeau Siemens-Severe Generalized) Recessive Dystrophic form of Epidermolysis Bullosa. So… go at it… ASK NICKY!!! Namaste! Post Views: 749Read More →