MY ALOPECIA STORY with photos - HAIR LOSS - Alopecia areata, totalis and universalis
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- Опубліковано 28 сер 2020
- Hi Guys, welcome to my channel! Here you can find both hair loss and pole fitness related content. In this video, I talk about my personal experience of alopecia (Alopecia areata, alopecia totalis and alopecia universalis) which started at aged 16. I hope this channel helps to spread some awareness to this auto-immune condition and help anybody experiencing hair loss themselves.
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I’m a man with alopecia universalis. Absolutely no relative that I know of has this condition. The benefits are: 1. I don’t have to spend money on hair care or shaving products 2. I don’t have to spend money on haircuts. 3. I don’t have to spend time in the morning shaving or getting my hair ready. It saves a lot of time.
Thanks for sharing. I have had alopecia universalis for nearly 20 years. 😊
Wow.. she's really pretty
I'm a guy with a thick beard & very long thick dense scalp hair (ofcorse they are, Im ethnically Asian after all & this is the one thing I always prided myself on) & noticed that i have various small patches in my beard after I got Covid. I'm in the last semester of university studying medicine & the cause of this disorder (Auto immune) crushed me mentally very brutally.....& is changing my personality for the worst i fear.....
Jess you’re so beautiful and I love hearing your story. I’m so proud to call you my friend... you are so strong xxxxxx
You are amazing Jess ❤️ loved watching your video, so brave and inspiring. Big hug xxx
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Your the most wonderful inspirational cousin, You are right it's your nans sister my aunt ❤ She's as strong and brave as you xx
I was just diagnosed with alopecia. I don’t know what type yet because it’s more of an overall thinning and not patches. I’m supposed to find out this week. I’m glad I found your video because I wanted to know how effective the treatments were. I’m not fond of medications.
I wonder if Alopecia is an Evolutionary thing....I am losing my hair too (Hair is retreating backwards across my scalp leaving no hair behind). No hair at all ever sounds fine to me :D...no more shaving my beard woot :D You are gorgeous...your Partner is super lucky <3
Thank you for sharing your story. I found it very helpful and informative.
Well done for highlighting this!
Are you okay? It has been a year since you uploaded a video . I am suffering the same . I understand you.
Thank you so much for sharing!
PLEASE Reply me 🥺 Can Alopecia Areata Convert Into The Alopecia Universalis 🥺 with time 😭😭 plzz Tell me About That I have alopecia areata
You not have any hairs how also please tell me sis
Have you tried the aip diet I have alopecia as well im trying the aip diet
Thank you for putting this video and for the detailed description. It must be a very tough expreince:( and I’m sure the video is very helpful for others. I would really be happy if you can give me your advice. I’m suffering from hair loss that started from nowhere,hundreds per day, from my scalp,eyelashes,eyebrows,and from all of my body. Almost 80% of my scalp hair and body fell out in 18 months. I don’t have bald patches but overall thinning. do you think alopecia areata can be the culprit? it sounds yours was more gradual. My nails turned yellow and have pitting(it was never like this). did you notice any change to your nails? Or other symptoms? because I have tingling in feet,hands,face,weight loss,extreme fatigue and constipation. everything is normal on my tests. my dr refered me to an endocrinologist because it sounds to him as an endocrine problem. Thank you🙏🏻
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