"As far as I know my white blood cell count is normal...I have regular blood tests and only the inflammation markers come back on the high side but even this has gone down lately and for the last 3 days I've been of prednisone completely.…"
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Deana DG
- Female
- Bristol, CT
- United States
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Deana DG's Discussions
What do you guys think I have AU or AT
Started this discussion. Last reply by kaye kirby Dec 9, 2011. 2 Replies 0 Favorites
I consider myself to have AU....I have no hair on my head, legs, arms or face. I do have to shave my under arms and the hair down stairs is there but is not much. My eye lashes come and go. After not…Continue
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Pat replied to Deana DG's discussion White blood cells and autoimmune diseases in the group M.A.D. (Multiple Autoimmune Diseases)
BTB (John) left a comment for Deana DG"Hi D i think this Tessy is a scammer she or he has messaged hundreds of members I got a message offering me pics and saying we should get to know each other etc etc the message varies for women but essentially its a phishing thing I am going to…"
Deana DG commented on Kaiana's group Alopecians with eczema"So I finally bought the Olive Body Butter and it is amazing. I have really bad eczema on my hands and I just got then olive butter yesterday and I can't even tell you all how much better my eczema is in just a day! Thank you so much Neil! I…"
Deana DG replied to Laura Adams's discussion Stronger immune systems? in the group Alopecia Universalis"I believe if you have no other autoimmune diseases or allergies, yes, your immune system is like a super immune system. That's how I was when I was young and first had AU. Unfortunately know that I am older and have other allergies I feel my…"
kaye kirby replied to Deana DG's discussion What do you guys think I have AU or AT"Hi Deana, you sound just like me and I have AU"
Deana DG commented on Kaiana's group Alopecians with eczema"Thanks Neil, I may try it. I am just cautious because I also have very sensitive skin."
Kathy D'Angelo replied to Deana DG's discussion White blood cells and autoimmune diseases in the group M.A.D. (Multiple Autoimmune Diseases)"Hi Deanna, When I was a child, my parents were told I may have leukemia, obviously a blood cell problem then. I lost my hair for the first time at 16, later went on to Addison's Disease, thyroid disease, and myasthenia gravis. I have had eczema…"
Deana DG commented on Carol's group Adults who have grown up with alopecia"Thanks Terri, for the summer I want to do a scarf or bandana but I want something i can tie in to a nice bow in the front....add the girly effect, but for the winter I have not found a hat I like that is also pretty. I tend to just wear my husbands…"
Deana DG commented on Carol's group Adults who have grown up with alopecia"Hi all, I am new to AW but have AU since I am 9. Like most of you have said it's just the way of life I know and have always known. I wear wigs when I go out because I feel it makes others comfortable and having worn one for over 20 years I…"
Deana DG joined Carol's group
Adults who have grown up with alopecia
This is a group for people who had alopecia nearly all their lives. The people who grew up with alopecia as children and still have it now as adults.See More
Deana DG commented on Kaiana's group Alopecians with eczema"Hi all, I have AU since I am 9 and eczema since before I could remember. I do notice a difference in my eczema with weather change and also with diet. I try to stay away from sugar and that started when I first had AU. As a kid it was so much easier…"
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- Relationship Status:
- Married
- About Me:
- Hello, I am 30 hrs old and have AU. It started when I was 9 with AA. I can't say it has impacted my life in a bad way. Growing up I still did things other kids did but then I wanted to keep my AA private and did all activities with caution. As an adult I could careless what others think. Although I still wear a wig but that is only because I would never want people to give me sympathy by thinking of me as a cancer patient, especially while out with my very young daughter. I am so happy I finally decided to see what groups are out there for AA because when I first lost my hair over 20 years ago there were very few groups. So thank you all for being here and sharing!
- Do you have alopecia?
- Alopecia universalis
- Are you age 18 or older?
- Yes - I am 18 or older
Comment Wall (3 comments)
- At 12:56am on January 14, 2012, BTB (John) said…
Hi D i think this Tessy is a scammer she or he has messaged hundreds of members I got a message offering me pics and saying we should get to know each other etc etc the message varies for women but essentially its a phishing thing I am going to report her to the coordinators John
- At 4:29pm on December 9, 2011,
LeslieAnn Butler said…
Hello and welcome, Deana!
How are you today? I have AU, too.
Leslie Ann
- At 2:17pm on December 6, 2011,
rosamosqueta said…
Hello, Deana! Welcome to Alopecia World. I have universalis too, and it´s good to share with others our experiences. Have a nice day!
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