"Hi Bon Thanks and sorry delay and you didn’t see my msgs on Seattle group page. I am sending you a private message with my number, on this site you can once people accept friend request. Or least that’s my experience and…"
"Hello Suzie, I guess I have to break down and create a Facebook account...I haven't because I have enough what I consider possibly invasive sites on my computer. At any rate, I will create one. I have to find another post on…"
"Hi again, I AGREE not enought hair dressers know how to customize faux hair! Luckily Collier Design in Seattle does just that and does it well. I am learning how to use the soft velcro wig band (?) to keep my wigs in place. So! I…"
"Good Morning All-mom thank goodness, so appreciate you friending me! Any advise you have re: faux hair is appreciated and head wraps, etc. I still have hair but profuse loss scarring around hair line. Have rare form; Lichen Planoparlisis…"
"Good Morning Lea, this is Bon still not sure how this site works. I have been so busy learning about my 'condition' that I haven't been able to spend enough time perusing it. I REALLY want to connect with the Seattle group…"
"Yes, I would attend. Just been diagnosed with Lichen Planopaliris. Tough to hear. I live in Everett and don't care for driving long distances but I will. I've tried to get responses on this site to no avail. Perhaps…"
"I would attend for sure. I live in Everett and don't like driving long distances but I have just been diagnosed with Lichen Planopaliris. I have tried repeatedly to get a response from someone but perhaps since I'm new to this site…"
I am most interested. I had beautiful thick curly hair but as a former cosmetologist I have always liked faux hair to change out my style and color.
Just diagnosed with Lichen Planopaliris...rare. Anyway, am moving into acceptance.…"
Find a shampoo that is all natural.....like Castile at a co-op or natural grocery store such as Whole Foods. I've tried every shampoo every high end essential oil.....you name it. I've found CBD oil to be very…"
I am learning my way on this website trying to connect with your group. I live in Everett. Last week I was diagnosed with Lichen Planopiliris. A rare form of scarring hairless/alopecia. The photo was taken in 2017 I don't…"
Hi Bon Thanks and sorry delay and you didn’t see my msgs on Seattle group page. I am sending you a private message with my number, on this site you can once people accept friend request. Or least that’s my experience and couldn’t before. Please call or text me. Thank you & good thoughts your way -know is challenging!
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.
AlopeciaWorld.com: It's hair loss support at its best!