Hi Dense,

I wanted to welcome to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us.

Cheryl

HI Denise,
We have the same name, I go by Dee. Hope you are having a great day!!

Hi Denise,
Nice to meet you. I am the same Dotty that posts the inspirationals on MSN. I also am good friends with Micaela(Flgirl). I miss her so much. We have been trying to get together since she moved to Boston. Hope to get to know you much better.
Love and Hugs,
Dotty

hei, Denise, glad to hear that your sports are not longer there....I gave up with the injections, but not with my hope! Let's meet again soon at our support group.

HI there, I think you will learn alot by reading others profiles! This is a great site!!!

Hello Denise I'm a mother of two whos youngest daughter twelve began going bald last Easter 2007 no hair anywhere now, I'm like you and don't know whether to accept this and get on with it or are there people out there who have had this, and now have a full head of hair? What things work what things don't work?
Good luck keep me posted !!! Di

Hello,Denise

Thanks for the suggestions about Aldera cream. I haven't heard of it but looked at the web and found it interesting. As you said, there is not a evidence-based therapy studies other than the shots and minoxidil, and some works for some people and others not. Glad to hear that your experience asking for God's healing was a truly one. Personally, God always work on my heart at such time of discouragement from the AA, and He promised me that " He even counts the hair on my head". I am so glad as I would already missed the count! Hope to see you again at AA meetings. And thanks for the cream suggestion: by the way, who prescribed it to you, a dermatologist?
Silvia

Thanks Denise for the comment left re my 12 year old daughter, tomorrows a big day her teacher is going to share with the class her predicament! so hope that goes well for her, shes a great kid, who has dealt with this issue soooo welll!!!! I'm very proud of her. At this stage we are not undertaking any treatment just hoping when her teenage hormones click in they might get the ball rolling Regards Di

Hi Denise,
Hope all is well with you and yours. I haven't heard of the Celiac Disease thingy but it doesn't surprise me at all. But, now that you mention it, I somehow remember that a friend of mine had been diagnosed with it and had an issue with hairloss for a bit but it stopped before it got bad. Hope this helps and thank you for the nice comment. Chat soon my friend. Love and Hugs, Dotty

Hi Denise,
How are you doing? I've had aa for 30 years.
LeslieAnn

This little doggie is Darby, a pomeranian puppy. When my son first brought him home, (a surprise to me) I thought he had AA or was in the process of AU. However, the vet said he had mites. His hair loss was extensive, no sores or anything, so it looked just like my AA spots, but much, much greater. Anyway, after we applied a liquid between his shoulders twice, his hair has started growing back. He will one day look like a big ball of fur. Anyway, that is why his picture is on my Alopecia World page.

I haven't...but I was wondering if the support group in B'ham will continue or has just stopped. I wish we could get together again.

Hi, Denise. Thanks for sharing the MSN AA message bord, I will check it. I still have 2 large areas with AA. My dermatologist does not want to prescribe the Aldera cream, and I do not want the steroids shots because of their side effects and mainly because they were not effective anymore. So I am using Rogaine, and not thinking too much about it. I am swimming laps this Summer with my kids at the public pool and decided not to wear any hat to cover the areas. It seems that nobody notice, or if they notice my bald spots (which certainly they do as they are very visible), there is no comment. What I have learned during this journey is that we are wonderfully made by God, and what happens with our physical body does not identify us as who we are. It is so important to accept ourselves with ou physical limitation.... Thanks for praying for me. I will keep you in my prayers as well and do not worry if/when the AA com back: He is in control.
Have a great weekend,

Silvia

Hi Denise,
Thank you so much for the love and support for Kristin. She got home from the hospital yesterday and I had my first good night sleep in 10 days!!! Everyone's thoughts and prayers have truly been heard. Thank you!!!
Love and Hugs,
Dotty

Denise, that is the cutest little doggy!

Hei, Denise! I will certailnly let Andrea know of changes if the group comes together again. I am doing OK, but my alopecias are increasing and I have an apointment with the dermatologist for October. I guess I am part of the resistant group:-) Glad the Lord sustains me, and know every single hair that falls.
Take care and keep writing,
Silvia

Oh thank you for the story about Darby! Give him a big cuddle for me. My dog Huey says hello too!

Hi, Denise.
So good to hear form you. I have not heard of the AA support group or Andrea....I am still fighting the AA, and I was diagnosed last week with AA difuse, all over the head. But the Lord is so good that HE still alows me to keep living and nowbody notice my hair style covering all the spots! I went for dinner with my husband yesterday and he said: your hair looks so good! The dermatologist is trying a new natural medication on the scalp( stearic acid), and I am using it all over my head.
I started a new job which is a real blessing to keep my mind off.
Have a happy New Year and remember to count your blessings. Always,
Silvia

Hi Denise,
Thank you for thinking of me. My holidays were wonderful. We got to see my hubby's family in North Carolina. Although, I didn't get to see my older daughter Kimi for the first Christmas ever in all of her 27 years! (she couldn't get the time off work). I hope all is well with you and your family. I think about my Alopecian family daily and send up prayers of peace and hapiness. Love and Hugs to you my friend and please keep in touch.....Dotty

Hey, Denise
Just reconnecting to the alopecia world again. So glad to find you message . Amazing to learn about your family history of alopecia. I never heard in my family. I was doing fine until this July, when suddenly hair felt non stop. I went back to UAB to see my dermatologist, and we are trying an old treatment that has been used in Europe and Canada. I bought a real hair wig to use at work, but stay bald at home and using hats. It was a hard hit emotionally again.

Hello my friend.....thanx for the message. Thinking of you and hoping all is well. Happy Halloween and hope the upcoming holiday season is wonderful.