Hydrocephalus Awareness Month

It is the thirtieth day of Hydrocephalus Awareness Month and I would like to share what I have learned over the thirty days of doing these posts. What I have learned from doing these posts is, that more people tend to read them and like them after I post them and then post them on Facebook. I've learned that I am helping people understand and educating them on what Hydrocephalus is. I feel that talking about it and writing about it has helped a lot of people understand what people like me have to live with. Hydrocephalus doesn't have a cure but it needs one. The only treatment for it, is a shunt. September is Hydrocephalus Awareness Month and It Matters. People like me living with It Matter. I hope you have enjoyed reading these posts, and I am glad that I can share them with you. I may continue doing these kinds of posts because it seems like, that's what keeps my followers or other people I don't know who may have found my blog interested in reading it. Help find a Cure. Spread Awareness and help someone understand what Hydrocephalus Is. Hydrocephalus Matters. I do too, along with everyone else like me who are going through the same things I am. Remember this, It is sometimes a struggle for those like me to have to go through surgeries so many times because their shunt malfunctioned. I am thankful I don't have to go through that many but for those who do, we can pray that they won't have to go through that again. Also remember for those who are like me, it is also hard for us to make and sometimes keep friends. That I think is hard for me, because I feel left out sometimes. I'm pretty sure that kids like me feel that way too, sometimes. This Month Matters.