Where acceptance is all there is!
I have been getting Kenalog 10 ( injections of steroids) for about the past 5 months. I go every month on the exact day. I have notice only in spot hair growth, however every time I go I also notice 2-3 new bold spots and some older ones just spreading. I get sick every time I get the injections ( head hurts, nausea, dizzy) I just cry, not to mention the side effect of the dents in the skull ( Atrophy) . I started to get panic attacks and major anxiety that led me to the ER. I am now taking beta blockers and other medication due to the stress of having alopecia and receiving the injections. My question is, should I stop the injection and just let the hair take its cycle of falling and hope it returns some day? Can I be comfortable being bold, how can any get through this. I need help, its a first for me and I just want to cry.
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Hi,
I am suffering from Alopecia Areata since 2 years.As suggested by doctor at the initial stage, i.e 2 years back I was given injection in my scalp(Kenacort injection). Within a week after taking the injection, my hairs started falling rapidly and I lost 100% scalp hairs as well as 70%body hairs. After that I never took injection. Started and tried lots of home remedies and ayurvedic medicines. Now 60% of hairs are back. Waiting for rest 40%.
So I suggest not to take injections.
Thank you all for response. I agree about the stress thing, I was NOT stressed when this all started, in fact I was the happiest I can remember. I did stop the shots and that's when I notice my stress, anxiety, and health started feeling better. I think I will invest in a wig so Chris for hair yes I would like more information. Thank you all I have found that this website helps me so much, I am learning to cope with this. My AA is a bit more worse then it actually says when you research info, I currently have more bold spots then it says and they are spreading I can see myself going bold.
Wow, Please take Deb's advice with a huge grain of salt....and really everyone for that matter. It is NOT caused by stress. It "may" be related to stress, but it is not caused by it. Many of us got AA at a time in our lives where everything was great and didn't have a care in the world. I can say for certain, that my AU is NOT caused by any stress. Also, do not listen to her about "you should continue the injections". It's your body, and only you know how you feel and how your body responds to the injections. My AA responded to the injections for about a year, then it didn't. My sister also just recently got diagnosed with AA (10 years after me). Stress? I think not.
Not going to lie and say this is going to be easy to deal with. It will be an emotional roller coaster as you learn to cope. But I promise it will get better. The best thing you can do is to surround yourself with loving, supportive people. Learn to be open about in front of them first, then you will learn to be comfortable in public.
Or....maybe Deb has a certain incense or candle flavor that can help all of our hair grow back along with playing in the park with children, then we'll all be cured!?
While I do believe that any chronic condition is exacerbated by stress, this does not mean that stress is the cause. Our immune system's can get knocked out of whack by many things. I do agree that the shots are not worth the side effects you are experiencing. They could have life-long changes to your body that you are not thinking of at this time but down the road might be very important.
BTW, I noticed you are from a town where I have a client that I am sure would be willing to connect with you. She has been through most of what you describe. if you are interested contact me through my site www.thehairreplacement.co
What's more important, hair or your health? Even if the injections work, it could be only temporary; I thought the shots worked for me, until they didn't. Your hair loss may or may not be caused by stress; how anybody can definitively say your AA is caused by stress is beyond me. I think the condition is different for everyone. I have zero stress in my life, yet I was diagnosed w/AA at 58; my hair came back twice, but it progressed to AU 3 years later. Some people get their hair back, some people never do. All of us probably try whatever "solutions" medical science has for us, but the truth is, your hair will either come back, or it won't.
I found having hair only to lose it again more stressful than giving up and living without it. I have always been open about my AA/AU with friends, family, new friends, strangers; everyone has been supportive and I find being open and talking about it therapeutic (but that's me).
Personally, I don't like wearing a wig; I do, I've gotten used to them, but they are not my preference. I can wear a hat all day, but I can only wear a wig for a few hours. I wish I could be comfortable going without something on my head, but I'm not. I prefer some kind of head covering and have soft caps for comfort and hats and scarves if I want to be more stylish. You just have to do what's comfortable for you.
Good luck to you.
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