r/alopecia

Dating with Alopecia Totalis: Does the Fear Ever Go Away?

I could really use some perspective from people who’ve been in a similar situation.
I’m talking to a guy who honestly checks every box for me, and then some. We met on a dating app, we’re long-distance, and things have been going really well. During the first week, I told him I have alopecia totalis. I don’t have hair, eyebrows, or eyelashes. He was incredibly kind about it and said it wasn’t an issue because he felt we had a genuine connection.
His response reassured me, but I’m still scared.
I’ve never been in a real relationship before, and I keep wondering what it’s actually like for people with alopecia or similar conditions to be in one.
One thing I can’t stop thinking about is the little everyday moments. I love wearing makeup, and it gives my face more contrast. Without it, I don’t think I look ugly, but I do feel like I look unwell, which makes sense given my condition. I’m nervous about things like waking up next to someone for the first time with no makeup, no eyebrows, no lashes..just me.
How did you navigate those fears? Did they ever go away? If you’re the partner of someone with alopecia, what was your experience like? And for anyone who has a visible condition, how did you learn to feel comfortable being fully seen by someone you cared about?
I’d really appreciate honest experiences, whether they’re encouraging or challenging. I just want to know what real life looks like.

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u/Sad-News3530 — 1 day ago

‼️15mo-old with extremely sparse hair, eyelashes, & eyebrows, despite visible follicles and normal blood work‼️BALD BABY GIRL ‼️

Hi moms ❤️

I’m looking to see if anyone has had a child with a similar experience.

My daughter was born with very little hair. Most of it fell out during her first 3 months, and now she is 15 months old and still has extremely sparse hair — I would estimate around 90 hairs on her entire scalp.

We have seen a dermatologist, and according to the doctor, the hair follicles are present and visible. The scalp doesn’t appear scarred, and there seems to be potential for hair growth, but very little hair is actually growing.

Her eyelashes and eyebrows are also very sparse. They are present, but there are only a few of them.

She has a history of eczema and cow’s milk protein allergy. We have also done blood tests, including thyroid function and vitamin levels, and everything came back normal.

One dermatologist suggested a possible explanation: that there may have been pressure on her neck while I was pregnant, causing reduced blood flow to the scalp, and then a sudden increase in blood flow after she was delivered by C-section. However, no other doctor has agreed with or mentioned this theory, so I’m not sure whether it makes medical sense.

Has anyone had a child with very delayed hair growth like this? Especially if they also had eczema, allergies, or sparse eyelashes and eyebrows?

Did the hair eventually start growing later on? I would really appreciate hearing any similar experiences. ❤️

Thank you so much.

u/dianaumkaram — 4 days ago

Hair growing back after 19yrs of alopecia universalis - weird sensations

I lost all my hair when I was 17, and had some level of alopecia for a few years before that as well. My hair has started growing back in the last year, aged 36 (no meds, just naturally).

Seemingly alongside this, I keep getting brief sensations on my skin, like crawling, or a breeze when it doesn't make sense. I'm wondering if its due to my brain not being able to process the slight information from the hairs? I keep thinking there is something on me (e.g. an insect), and feeling the need to brush something off with my hand. However, this isn't entirely inline with my hair growth - e.g. I've gone from zero leg hairs on my right leg to three visible hairs on one side of it, but I sometimes feel sensations on the other side of it. I don't know if this is because my skin has slightly changed in preparation for hair growth and I'm just feeling micro changes in the air that the average person is used to and can block out... Or if this is completely unrelated.

Has anyone else who hasn't had hair for a considerable length of time experienced this?

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u/Maleficent-Bet9660 — 5 days ago
▲ 6 r/alopecia+1 crossposts

Vitaminas q influyen en la caída del cabello

Gente quiero saber q estudio de sangre se hace para saber q influye en la alopecia y caída del cabello.

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u/El73rko — 6 days ago

Is it normal for spot to grow and have regrowth and diffuse shedding?

my spot has grown in just a few days and i’m wondering if this is normal? has anyone experienced diffuse shedding and a patch of hair loss? I know i am in an active flare because 1. the spot is growing 2. it feels burny and achey on my scalp. how long do flares last? i am trying to trust the process but im freaking out because i see my hairline changing too! thoughts on minoxidil?

u/Buffalochips1133 — 8 days ago

Female androgenetic alopecia – Has anyone had success with supplements or safe treatments?

Hi everyone,

I have androgenetic alopecia and I'm looking for advice from people who have actually found something that helped.

Has anyone had success with supplements such as biotin, or any other products? Are there any treatments that are considered relatively safe and low-risk?

The problem is that I have heart arrhythmias, so I'm quite worried about using minoxidil because of the potential cardiovascular side effects. I also have hormonal issues, which may be contributing to my hair loss.

My hair loss hasn't progressed too far yet, but my hair has become extremely thin, fragile, and breaks easily. I'd really like to do something before it gets worse.

I'd appreciate hearing about your experiences, what worked (or didn't work), and any suggestions I could discuss with my dermatologist.

Thank you ❤️

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u/Ok_Attention_7263 — 11 days ago

minoxidil for traction alopecia?

I’ve had braids for seven years straight and I am giving my hair a break now because my edges are thinning. I have been looking into minoxidil but I’m not sure if it works for traction alopecia or if it’s only for hormonal hair loss. If you used it for your edges would love to hear experiences.

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u/Teelaikhumbi — 13 days ago
▲ 3 r/alopecia+1 crossposts

Hair dye with FFA

Hello all!

I was officially diagnosed with Frontal fibrosing alopecia (FFA) back in November 2025 via biopsy. After 3 rounds of steroid scalp injections and then getting put on Hydroxychloroquine and using liquid minoxidil daily.

I haven't dyed or bleached my hair since Sept 2021. I am in a spot where I experience I want to go back to doing some hair color/highlights.

I am looking into just doing either straight pigment color drops or semi-permanent type color over my natural hair without any bleach etc.

Has anyone had recommendations for brands to use?

I went through Gemini for some ideas that wouldn't irritate (since I'm avoiding it going directly onto my scalp), but the brands are either hard to get or don't have the color I want.

I am perfectly fine with something that washes out and just does a tint

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u/Mcburgerdevil — 14 days ago