Susan Innes
  • Female
  • Waunakee, WI
  • United States
Share Twitter

Susan Innes's Friends

  • Chris
  • Emz
  • Edward Brown
  • N
  • Debbie
  • N. Rana
  • Jean
  • ziba
  • imtoosexyformyhair
  • Katie
  • lunablue
  • Deborah
  • godfreygirl143
  • Figarosmom
  • sendrifter

Susan Innes's Discussions

Anyone aware of Harold Battiste Jr., New Orleans Jazz Musician?

Started Nov 16, 2011 0 Replies

Hi- Someone special is featured in AARP magazine, November 2011 issue. His name is Harold Battiste Jr, a New Orleans jazz musician who at the age of 80 is still actively participating in his music.…Continue

Gifts Received


Susan Innes has not received any gifts yet

Give a Gift


Susan Innes's Page

Latest Activity

Susan Innes commented on Susan Innes's group Alopecians in Wisconsin.
"Hope love, compassion and kindness is bestowed upon all of you over the holidays, and thanks Josh and Kiah for all of your wonderful events and support! Susan"
1 hour ago
Susan Innes left a comment for Jolene
"Hi Jolene. I'm sorry about your hair loss but glad that you found the website. There are many with whom you can share your frustrations and heartbreaks. If you'd like to see others from the Wisconsin area, please click on the groups block…"
1 hour ago
Susan Innes left a comment for Ann Wilson
"Hello Ann, I confess that not only is this to welcome you to Alopecia World but your little Shih Tzu as well. My family had adopted Shih Tzu rescue dogs for years but one of the two last adopted had alopecia universalis. Of course, no one wanted the…"
1 hour ago
Damani commented on Susan Innes's group Alopecians in Wisconsin.
"Josh. Wishing you a great meeting tonight. Unfortunately with schedule changes, I won't be able to join, tonight. Appreciate you and your leadership!"
Dec 4
Josh and Kiah commented on Susan Innes's group Alopecians in Wisconsin.
"Hey all here are the details of tonights support group meeting. Hoping some of you can make it. "
Dec 4
Susan Innes and Chris are now friends
Nov 15
Susan Innes left a comment for Marlee Hutchison
"Hello Marlee, I'm very sorry to hear that the condition is now becoming worse. It's only been 2 years since the total loss so it's relatively soon to be able to accept the change but the day will come when the hair will not be the…"
Nov 15
Susan Innes left a comment for Tina
"Hi Tina, Welcome. Several of my friends have this type of alopecia; in some respects I think it's more difficult than universalis. I hope you were able to find a good hairdresser to help with the problem. We have a special group for those of…"
Nov 15
Susan Innes left a comment for sarbar
"Hello - Glad that you decided to become a member of Alopecia World. There is a group at this site for Wisconsin residents called "Alopecians in Wisconsin" ; we'd love to have you join us. Susan"
Nov 15
Chris joined Susan Innes's group

Alopecians in Wisconsin.

A group for Wisconsinites to meet and greet. We also welcome Wisconsinite friends and folks who have been here and love our state as we do. Remember if you don't have anything kind to say about our Midwest accent, best not to say anything at all:).See More
Sep 26
Chris left a comment for Susan Innes
"I would love to join the group from Wisconsin.  It would be great to talk to other people who have AU."
Sep 26
Susan Innes left a comment for J-me
"Hi J-me, Welcome to Alopecia World. I just returned from a trip to Brainerd, MN, passing through your lovely area. I hope despite this disease, you've been able to enjoy this beautiful September. I'm living in the Madison area but we have…"
Sep 25
Susan Innes left a comment for Chris
"Hi Chris, Welcome to Alopecia World. If you'd like to see others from Wisconsin, there is a group entitled Alopecians in Wisconsin. We are from all over the state and of many ages. There are some announcements on the site regarding fundraisers…"
Sep 25
Susan Innes left a comment for Kathy
"Hello Kathy, Welcome to Alopecia World; I'm from the Madison area. A few years ago in order to perhaps help keep the Wisconsin residents informed of local groups and/or meetings, I created Alopecians in Wisconsin which can be located under…"
Sep 25
Susan Innes left a comment for Hosch
"Welcome to Alopecia World from a fellow Madisonian. I'm sorry that we're communicating because we share severe hair loss. There are quite a few of us in Wisconsin so I started a group here called Alopecians in Wisconsin that we'd love…"
Sep 25
Josh and Kiah commented on Susan Innes's group Alopecians in Wisconsin.
"Hey Josh. Not positive when next support group meeting will be. We just finished held or big fundraising event, Rock for Locks and Morgans Ride for Alopecia last weekend and are still wrapping that up. We do however, have another event tomorrow.…"
Sep 11

Profile Information

Relationship Status:
About Me:
Retired art educator and medical transcriptionist whose retirement includes drawing, painting, and rescuing small dogs. Some of my favorite places are the local dog parks:).
Do you have alopecia?
Alopecia universalis
Are you age 18 or older?
Yes - I am 18 or older

Susan Innes's Photos

  • Add Photos
  • View All

Comment Wall (47 comments)

You need to be a member of Alopecia World to add comments!

Join Alopecia World

At 12:49pm on September 26, 2014, Chris said…

I would love to join the group from Wisconsin.  It would be great to talk to other people who have AU.

At 12:29am on October 13, 2013, N. Rana said…

You're welcome!

At 11:33pm on August 16, 2013, Mary said…
Susan, I am having a bit of trouble navigating the site. Thanks for your post...I will join the WI group as soon as I figure out how to
At 11:05pm on August 16, 2013, Mary said…
Susan, Thank you. I am having some trouble figuring out how to navigate around the website, leave comments, or join groups. It probably doesn't help that right now I am out of town & on a slow internet connection. I will join the WI group when I figure out how to do so.
At 4:56pm on May 23, 2013, Michelle said…

Thank you so much, Susan! I was intending to join the Wisconsin group, as I would like to get to know some people in my own neck of the woods. I was first diagnosed with AA in March, and now that I'm seeing it progressing, I'm starting to really need support from others who suffer from this, too. I really appreciate your reaching out -- it's so good to know we are not alone! :)


At 12:49pm on May 15, 2013, bkundert7 said…

Thank you for your kind words. I really appreciate it! I am so glad there is a group in Wisconsin. I would really like to join. I has been very stressful going through this alone. I am so glad I found this website :) We should definitely meet sometime. I am in the process of moving to another place in Madison so maybe this summer we can get together. Thanks again for your support!

At 12:29am on February 22, 2013, DANNI said…
Thank you Susan for inviting me to your group I appreciate it! :)
At 8:29am on January 24, 2013, Debbie said…

Hi Susan,
After a long day at work I went home and had myself a good cry last night. I am feeling better this am and ready to take on a new day. I thank you and others on this site for helping me come to terms with the fact that my hair mostlikly will never grow back. It helps to know their are others that are like me,and look forward to the day when I can help someone else who is looking for support.

At 3:42pm on January 23, 2013, Debbie said…

thank you ,Susan would love to join the group from Wisconsin :)

At 6:18pm on November 19, 2012, Jean said…

Hi Susan,
Thank you for the words of encouragement!
I have 2 wigs, but have found them to be very uncomfortable, hot and itchy. One was very expensive and one not. My husband has been a rock through all of this. He understands when I have my crying jags and just sees me through it all.
I am considering seeking the help of a counselor, and do have some names from my doctor. I just haven't made that step and I don't know why.
It's nice to have found this website. The other one I used only asked for money, which if they really thought about it, we spend most of our "extra" money trying to find ways to have hair!





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. It's hair loss support at its best!

© 2014   Created by Alopecia World.

Badges  |  Report an Issue  |  Terms of Service