www.alopeciaworld.com
I wouldn't say I'm out of the woods yet but my big bald spot has been noticeably filling in, maybe due to my nightly clobex use and periodic kenalog shots (or maybe it would've happened anyway - who really knows?). The thing is, my scalp is still pretty itchy, even in parts where I've never lost any hair. The dermatologist says it's part of the autoimmune reaction which is worrying because if I'm still itching does that mean I could start losing hair again at any moment? If or when the autoimmune reaction is really over will the itching end too? So far it's been eight months since I discovered the bald patch and the itch isn't as intense but I still feel it at various times every day.
Tags:
Thank you, Dawn, for those suggestions! It's good to hear I'm not the only one but it's such an irritating thing. I've been using a sulfate free shampoo since discovering the bald patch. It's L'Oreal Everstrong and it really seems to work in strengthening my hair. I used to always lose so much when brushing and combing (even before being hit with alopecia) so I wouldn't want to change that out. The only other thing I use is an awesome detangler called It's a Ten. Whenever I skip it or switch in another detangler, I lose LOTS more hair (which is fairly long) during brushing and combing which is obviously the opposite of what I'd want. My hair has always been super fine and tangly and I use to basically railroad through it to the degree that now I have to wonder if what I have is not alopecia areata as diagnosed but some kind of traction alopecia. I'm super, super careful with it now but since the minimal products that I currently use seem to be helping me maintain the hair that I do have (no more has fallen out since I found the large patch last January) I'm reluctant to switch at this point. It's just the itch that's a problem. Has you hair grown back or is it in in the process of growing back too? Sending luck back your way and thanks for the suggestions. I'm bookmarking thing to keep tracking of the shampoo name.
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.
© 2024 Created by Alopecia World. Powered by