So I’ve been dealing with PPMS for a few years now, and nothing has been easy. I don’t need to go through the extended list of side affects with you, because I’m sure we all suffer from this neurological monster in a very similar manner. I’m most concerned with where it has left me as a young father of two very young, wonderful and active boys.. I want to provide for them and give them everything I can. Unfortunately, I feel myself slipping away, both physically and mentally. The difficulty of these last few years have been a massive strain on many of my relationships, to say the least. As we all know, an invisible illness doesn’t garner much sympathy or understanding. I wish there was something I could do to bring more awareness of the affect this illness truly has on us, and those around us. I would travel the world to enlighten those who really don’t know of how serious and crippling MS is; but unfortunately I would be exhausted after about 15 minutes of a presentation… 🙃🙃 🤣