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I got up this morning, got a shower and tried to style my hair like have have done my whole life, only to end up in tears when I tried to blow dry what is left of my pathetically thin hair. I finally gave up trying to style basically nothing, and plopped on my topper to hide the stringy mess. I just don't know how I am going to face the rest of my life with this condition. It seems like there are no treatments that work and very few success stories once AA had reached an advanced state. I just feel like crawling under a rock and disappearing. Sorry for being so depressing, I just feel so blue today.
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Well....remember you are going through a process of grief. which can take time and has its ups and downs. I still have moments when I wish I had my soft comforting hair back, yes. however, the pain of loss gets less and less. There are also times when I like being bald (like when it is super hot) and when I feel sexy with the new look. I am one of the 5% I have read about that start with patches and lose pretty much all of their hair. So pretty sure I am not getting it back. I have come to terms with that for the most part. You, however, might not lose it all. Which in some respect might make the journey more difficult because you have that emotional weight of not knowing hanging over you. Keep reaching out, talking helps.
it is interesting to me that you were taking acutane, because I was too. I have wondered if that had anything to do with the hair loss as they have correlated it with other autoimmune disorders.
Keep looking up - God is looking down!
I have been agonizing over getting a wig for months now. I could not get a topper. My hair loss on the sides and starting on the top now. I could cover it with my own thin hair, but it looked like crap. I went to a wig salon yesterday in Denver and bought two wigs. My husband thought I would not wear it if I bought it. Anyway, I wore it home and loved every minute of it. I felt like a huge weight had been lifted. I wasn't afraid to be in the wind. I wore one to church this morning. I got four compliments at church. People came up and told me they like my hair. My son was shocked how natural it looked and how much better I looked with hair. One person even said I looked gorgeous. I haven't felt gorgeous for months, but today I actually felt great. I don't like the fact I have to wear a wig, but now I can concentrate on getting my hair to grow back. Before I worried about it too much. I could not use any therapy in the morning because it weighted my hair down. Tomorrow I am going to wear it to work for the first time and I even have to conduct a staff meeting. Believe me, I have to ask for strength from the Lord to get through this, but just ask and he will help you. I want to start smiling again. I think I can now that have hair! God Bless.
I got a synthetic wig to start with. Yes I was very nervous wearing it to work. Everyone liked it and they knew it was a wig because the color was different than I normally wear. I'm lucky to have support coworkers. I told them about my diagnosis immediately.
Right now I am undergoing cortisone injections, had my first ones about 3 weeks ago. I wanted to use Rogaine in the a.m. and p.m. to see if that would help. I am also trying aromatherapy. I wear hats with my own hair or scarves. Some days I don't wear the wig and just try to do the best I can with my own hair.
I bought a Raquel Welch wig. For my first wig I guess it is okay, but my scalp was itching with it. I did not want to spend too much the first time, but maybe it would be worth it if you get something comfortable and that you feel good in. Keep me posted on your journey and God Bless!
I feel your pain. It has been since 2009 and I struggle each day. Why? why me? why this? can people tell? or this wig is wrecked . the money I have spent on wigs is approx $4,000.00 and over 12 wigs later.............Just keep looking and you will find diff ones to try and there are some nice ones. I really miss swimming under water. I do not go out bald, only at home when I have headaches cause wigs hurt your head when you have a headache. I shave my head as It is depressing to see bald spots & then some shadowed hair spots that never grow enough, and you know the whole time that it will not come back and then the fear of ok, if it comes back "could I be in line at the bank and a huge part of it will fall out again?" NOt worth the stress....... I really struggled when my eyebrows and lashes fell out that sucked, but I now wear eyebrow wigs they make me feel better. SO yes today was a bad day, but tomorrow will be better. Hang in there. And remember you are alive and this can be lived with. It is not easy I won't lie but Alopecia is life altering not life threatening this I keep telling myself. It helps me get thru the bad days. I gave up on the shots they hurt too much and made me sick for the whole day. Well Your not alone. :) I wish I could wave a wand and make both of us back to what we use to be...... But I cannot. :) Journal, talk with family and friends but do not keep your feelings in. :) Thinking of you Denise
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