New to forum(3)

Cherjer

 For the past 4 months I have been reading all the posts and have finally got the nerve to join. My husband was diagnosed with AD in 2015. I must admit I thought there would be a cure in the near future. Our neurologist was on the "cutting edge" of a cure...a scientist besides being a great neurologist. We were able to do a lot of traveling and enjoying our family and friends. However, I came to the realization that there will never be a cure in my husband's life time. He has the APO 4 gene which makes me nervous about my son's chance of AD. Right now my DH is showing great progression. I am not sure what stage he is...I appreciate all the knowledge that I have gleaned from this site and thank you all for giving me insight. 

Sorry I posted on the wrong place!!

M1

No worries, and welcome.  This is an excellent place to share and learn.  Good luck....sorry for your need to be here.  Each journey is the same, but individual.  What's the saying--you're unique, like everyone else?!?

Cherjer

Thank you! I noticed that it says I joined in 2016 but that is incorrect...just joined in 2021!

janeymack

Hello, and welcome! Not one of us wants to be here, but at least we have each other. My H was diagnosed EOAD in 2013, at age 60, and has progressed slowly, until recently. He's now firmly in Stage 5.