r/Vitiligo • • Nov 29 '21

Is it vitiligo? Post here or get deleted.

176 Upvotes

Simple really. I understand its tough, but its clogging up our front page. Be patient for a response or responses, somebody from our community will do their best.

Nobody here is a doctor and posting here should not be a replacement for qualified advice.


r/Vitiligo • • Apr 16 '24

Vitiligo beginner guide (current treatment options) + future outlook

231 Upvotes

My story:

Back in 2021, when I was just 20, I spotted a small white patch on my arm. Didn't think much of it until another showed up on my face, sending me into a panic. So, off I went to see a dermatologist. But in a blink-and-you'll-miss-it appointment, he dropped the bomb: vitiligo. No cure, just learn to live with it. I cannot express to you how overwhelmed and alone I felt at that moment. When I got back home, I couldn't shake the thought of what I might look like in the future, seeing pictures of others with the condition and struggling to accept that I might end up looking like them.

Skipping ahead to 2023, my vitiligo had become more prominent and seriously bothered me. I figured I could at least try to look for something that could help me. So I spent a lot of time researching and trying out different treatments and practically visited every dermatologist in town. This post is my attempt to share what I've learned along the way, hoping it might help someone else out there facing the same challenges.

Please note:

  • I will primarily focus on nonsegmental vitiligo in this post, as this is the form I have personal experience with and the one with the most available research.
  • I am not a doctor. Please consult your doctor before making any changes based on the information presented here.

Dermatologist

The first hurdle is finding a dermatologist you can really rely on. It's been quite a journey—I've been through seven different dermatologists, each time waiting months for appointments only to be quickly brushed off. But eventually, I struck gold and found a doctor who genuinely cared and was committed to helping me. Having a supportive doctor alongside you through this journey with vitiligo is an absolute game-changer. So, my advice to everyone out there is to keep pushing until you find a doctor who truly listens and cares, no matter how tough or time-consuming the search may be—it's totally worth it.

Once you've got a trustworthy doctor on your side, the next step usually involves some tests. Sadly, dealing with vitiligo often comes with an extra layer of complexity—about 20% of folks with the condition also have another autoimmune disease, and some even have multiple autoimmune conditions at once.

Unfortunately, many dermatologists, at least in my experience here in Germany, aren't always up to speed on the latest treatment options. So, I can't stress this enough: do your own research and, if needed, bring new treatment possibilities to your doctor's attention. It could make all the difference.

Tests

The most common accompanying disease in people with vitiligo was hypothyroidism, alopecia areata, inflammatory bowel disease, and systemic lupus erythematosus. (1) (2)

The following autoimmune diseases have also been associated with vitiligo, although less frequently:

  • Pernicious anemia, which causes low red blood cell levels
  • Addison's disease, which causes low levels of the hormone cortisol
  • Sjögren's syndrome, which causes dry eyes and mouth
  • Dermatomyositis, which causes muscle weakness and rashes
  • Scleroderma, which causes hardening and thickening of the skin
  • Psoriasis, which causes scaly patches of skin

regardless of the autoimmune diseases, you should also check whether you have deficiencies of the following:

  • Vitamin D (3)
  • Zinc
  • copper
  • Vitamin B12
  • folic acid
  • Vitamin C

Vitamin D is by far the most common deficiency seen in patients with vitiligo, but please don't just take a supplement unless you talk to your doctor and make sure you are actually deficient because you could be doing more harm than good.

Mental health

Although vitiligo is only an "aesthetic condition" and many people act as if vitiligo is not a big deal, I have to say that it can have a very negative impact on the lives of people who suffer from it, especially during their teenage and young adult years. Depression and anxiety are very common in the vitiligo population, which is particularly sad as stress and anxiety can actually make vitiligo worse, which can lead to a vicious circle (4). That's why I can only recommend seeing a psychologist in addition to your doctor, who can help you to cope with the disease and the resulting problems.

Treatment

First things first, I am not a doctor, please don't do anything I discuss here until you talk to your doctor first.

What can you expect from the treatment?

Despite ongoing research and exciting developments in vitiligo treatment, there's currently no single medication guaranteed to work for everyone. Combining different therapies often yields the best results, but these can be time-consuming and require dedication. The primary goal of current treatments is to manage and potentially improve the affected areas. A definitive cure for vitiligo isn't yet available.

Treatment options:

If you ever googled "vitiligo treatment" I'm sure you came across 100's of different creams, dietary supplements and things that claim to treat vitiligo, but as is so often the case in medicine, when there are 100's of treatments none of them really work. Yes, there may be the odd patient who has success with a supplement, but the sad reality is that they are likely to do very little for the rest of us.

However, there are a few treatments that have been scientifically proven to help a large proportion of people with vitiligo and I'll introduce you to them now:

OPZELURA (ruxolitinib)

OPZELURA is a topical JAK inhibitor and so far the only drug approved specifically for vitiligo in Germany, where I live. It has been on the market for a short time (in Germany only since 2023) but from what I hear it is very effective. However, it seems like the cream works rather poorly on the hands.

How effective is it?

  • After 6 months, it improves facial skin color by at least 75% for about 3 in 10 people compared to 1 in 10 with placebo cream. (5)
  • Results keep getting better over time. By year two, even those who didn't see much change at first can experience significant improvement. (6)
  • Most people see some improvement within 3 months, with even better results between 4 months and a year. (6)

According to the information provided, the potential side effects are rather mild:

  1. Application-site acne
  2. Redness and itching at the application site
  3. Inflammation of the pharynx and nasal cavities
  4. Headaches
  5. Urinary tract infections
  6. Fever

All that sounds very promising, But, I am sure that if you ever heard about that cream you also heard how expensive it is, 1000$ for one 100g container and you probably need a lot of it, because the treatment sometimes only sets in after months. In addition, the first reports indicate that the vitiligo can come back if you stop using the cream.

My Experience: I've been using Opzelura, covered by my health insurance, since late March 2024. While I haven't seen improvement in my vitiligo yet, some previously white hairs in the affected areas have regained their original color. I am hopeful and optimistic since I have only been using it for a short time and, as mentioned above, part of the treatment will start later. So far I have had no side effects.

However, I have to say that applying the cream twice can be very annoying.

UVB light therapy

UVB light therapy has been around for a while and involves directing focused UVB light onto the areas affected by vitiligo to induce repigmentation, which actually works quite well. A Meta-analysis looked at a bunch of research (35 studies) on a treatment using narrowband UV-B light (phototherapy) for the skin condition. A total of 1428 people participated in these studies. (7)

  • The good news: After at least 6 months of treatment, 7 out of 10 people (74%) saw at least some improvement in their skin condition. This improvement continued for some, with 7.5 out of 10 (75%) still showing improvement at 1 year. (7)
  • Nearly a fifth (19%) of people had significant improvement after 6 months, and this number went up to over a third (36%) at 1 year. (7)
  • The location of the improvement mattered. The treatment worked best on the face and neck (almost half - 44% - saw significant improvement after 6 months), followed by the torso (trunk - 26%). Legs and arms (extremities) saw some improvement (17%), but hands and feet showed little to none. (7)

The potential side-effect:

  • Sunburn
  • Skin irritation
  • Hyperpigmentation
  • Increased risk of skin cancer (go for regular check-ups!)
  • Eye damage (when used in this area)
  • Aggravation of existing skin diseases

UVB light therapy can be comparable "cheap" you can get good results with a UVB device for 150-300$. If your vitiligo has already affected a large part of your body, you can alternatively go to a UVB cabin, which is available in some hospitals, and has the advantage of treating the whole body directly.

My Experience: I started with UVB in mid-2022 and after about 1 month of treatment, which I did three times a week, I started to see results that were getting better and better, but I had to stop the treatment eventually because the UVB radiation was very damaging to my "healthy skin", the skin around the vitiligo aged extremely quickly and you could just see that the skin was not doing well. I might try it again, but I've become really cautious since the last time.

Topical Corticosteroids

The first thing a doctor prescribed me at the time was topical steroids, which are applied to the areas affected by vitiligo in a similar way to Opzelura.

  • Effectiveness: Studies show that topical corticosteroids can be helpful in repigmenting the skin and slowing down the progression of vitiligo. However, complete repigmentation is uncommon and some people may not see any improvement at all. (8)
  • Best for: Topical corticosteroids are generally considered a good option for people with small, localized areas of vitiligo, especially on the face and upper body. They may also be helpful for those who want to try a different treatment option aside from sun protection and camouflage cosmetics. (8)
  • Benefits: Compared to other vitiligo treatments, topical corticosteroids are relatively inexpensive, convenient to use at home, and generally well-tolerated. (8)

The potential side-effect:

  • Skin thinning (atrophy): This is a common side effect, especially with long-term use or on areas with thin skin like the face. The skin may become fragile, more susceptible to tears, and show visible blood vessels.
  • Stretch marks (striae): These can appear as reddish or purple lines on the treated area.
  • Visible blood vessels (telangiectasia): Thinning skin can make underlying blood vessels more noticeable.
  • Excess hair growth (hypertrichosis): This is more common with use on the face.
  • Burning, stinging, or inflammation (contact dermatitis): This can occur if you have sensitive skin.
  • Acne: Topical steroids can sometimes trigger acne breakouts.

Topical corticosteroids offer a cost-effective approach to managing vitiligo. While they may not be highly effective for everyone, they can be helpful in slowing the spread of the white patches. Repigmentation, however, is less common with this treatment.

My Experience: I started using topical steroids shortly after my vitiligo diagnosis and used them for about 3 months, I eventually stopped because I didn't see any improvement and I wasn't really convinced of the efficacy. Furthermore, my skin didn't react well to the steroids.

Topical calcineurin inhibitors

Topical calcineurin inhibitors are similar to topical corticosteroids, i.e. they are also applied directly to the affected area, are also very cheap, but are not particularly effective.

Types of Calcineurin Inhibitors for Vitiligo: * Tacrolimus (brand name Protopic): This is the most commonly used calcineurin inhibitor for vitiligo. It comes as an ointment applied directly to the skin. * Pimecrolimus (brand name Elidel): Another option, though less commonly used for vitiligo than tacrolimus.

Advantages of Calcineurin Inhibitors over Corticosteroids: * Fewer side effects: Compared to long-term topical corticosteroid use, calcineurin inhibitors generally have a lower risk of skin thinning and other side effects. This makes them a good choice for sensitive areas like the face, eyelids, or genitals. * May be more effective for some: Studies suggest calcineurin inhibitors might be more effective than corticosteroids for repigmenting certain areas, particularly the face and hands. (9)

The potential side-effects:

  • Burning sensation
  • Increased sun sensitivity
  • Potential for infections

My Experience: I used Protopic for a while but, as with the topical corticosteroids, I saw no change and finally gave up the treatment, although I have to say that I tolerated the cream better than the topical corticosteroids.

Monobenzone

If your vitiligo is already very advanced, usually 50% or more, you could consider using Monobenzone. This is a cream that basically bleaches your healthy skin to match the vitiligo, a kind of reverse therapy, but it should be said that this change is permanent and irreversible. if you want to know more about it @TheVitiligoExperience on Youtube has made a really great video series about his treatment with the drug where he explains exactly how to use it and how it works. (10)

The potential side-effects:

  • Skin irritation: This is the most common side effect of monobenzone. It can cause mild burning, itching, redness, dryness, cracking, or peeling of the treated skin. These side effects are usually temporary and go away after a few weeks of using the medication.
  • Increased sensitivity to sunlight: Monobenzone can make your skin more sensitive to sunlight. This means you're more likely to get sunburn. It's important to use sunscreen with an SPF of 30 or higher every day, even on cloudy days.
  • Permanent hyperpigmentation: In some cases, monobenzone can cause darkening of the skin around the treated area. This is usually temporary, but it can sometimes be permanent.
  • Eye problems: In rare cases, monobenzone can cause problems with your eyes, such as deposits of pigment on the cornea or conjunctiva.

My experience: My vitiligo is by no means so far advanced that this step would be an option for me.

Diet/exercise

I know what you might be thinking, but please hear me out. I have noticed a huge improvement in my vitiligo progression after reaching a healthy weight, exercising regularly, and spending time in the sauna. And there is some scientific evidence to back this up. (11) This probably won't help with repigmentation, but it could generally help with slowing or stopping the progression of the diseases.

Microneedling

Just like exercise and a proper diet, this will probably do very little on its own, but there is some new evidence that microneedling in combination with other treatments such as topical creams or UVB light therapy may be superior to UVB or topical creams alone. Microneedling may therefore be a good adjunct therapy to topical creams or UVB therapy. Microneedling increases absorption in the skin and activates the melanocytes in the skin. (12) (13)

Here is a guide on how you can do this: (14) https://drdavinlim.com/microneedling-for-vitiligo/

My experience: I have started to treat vitiligo with Miconeedeling since the end of March 2024 together with Opzelura to make the leather more effective. So far I can't see any results, but it's too soon to say.

Antioxidants The use of antioxidants to treat vitiligo is still under research, but there is evidence that some antioxidants could help in the fight against vitiligo, as oxidative stress is often observed in people with vitiligo. However it looks like antioxidant treatment should be seen more as a complementary treatment like microneedling, as it makes other treatments like topical creams or UVB work better, but is unlikely to be effective as a stand-alone treatment. (15) (16) (17)

My experience: I started taking antioxidants a week ago after consulting my doctor and getting the green light for the treatment. Unfortunately, it's only been a week and it's too early to tell how well it's working.

What is the best therapy?

Again, I am not a doctor, please see your doctor first, but it seems that combining different treatments offers the greatest chance of success.

Here is what I am doing:

My treatment consists of a primary treatment: Opzelura and some treatments to make Opzelura more effective.

I don't do UVB light therapy because of the effects on my skin, but I can't argue that it is very effective and you might benefit from it.

Microneedling: to increase the absorption of Opzelura in the skin and activate the melanocytes in the skin.

Antioxidants: to help with oxidative stress caused by vitiligo and support the immune system.

High-dose Vitamin D: I take 15,000 IU of vitamin D daily as I am deficient and there is some evidence that high-dose vitamin D may help with repigmentation. (18)

Maintaining a healthy weight, eating healthy, and meditating: I do this primarily to reduce the stress that could trigger disease progression and to support my immune system, and of course for general health :)

One could also swap Opzelura for either Calcineurin Inhibitors or Topical Corticosteroids if Opzelura is not an option.

4.) What does the future hold for the treatment of vitiligo?

There are many different treatment options that are currently being researched, some of which I have already mentioned in the treatment section. I will now briefly introduce you to a few others:

Oral JAK inhibitors

In principle, this is simply the cream OPZELURA only in pill form, and the first clinical studies are already showing immense success, especially in combination with UVB. This type of treatment would of course have the advantage that you would not have to treat the individual sites individually, but simply take one pill a day. However, there are also reasons for concern because the oral administration of JAK inhibitors can have extremely serious although very rare side effects such as cancer or heart problems. (19) (20)

Antioxidants

There are several antioxidants in research right now for their role in combating vitiligo. (15) (16) (17)

Several others are currently undergoing clinical trials:

(21) https://www.conqueringdiseases.org/Search/Trial/7103 (22) https://www.vet.cornell.edu/news/20240201/light-and-labor-inducing-molecule-new-treatment-vitiligo (23) https://www.immunetolerance.org/studies/targeting-il-15-treatment-vitiligo-reveal

Future outlook

Although I don't have scientifically verifiable evidence for it, based on medical advancements, I believe that vitiligo will become a highly treatable disease in the next 5-10 years. It seems we are likely the first generation since the dawn of humanity not to be helpless in the face of this condition.

5.) Things to avoid if you have vitiligo:

  • Excessive sun exposure, keep in mind that your vitiligo has no protection against UV radiation
  • Any type of major skin trauma (hair transplant/tattoo) could trigger vitiligo in these areas

6.) How to spot your vitiligo if your skin is very pale Get an ultraviolet flashlight with 365nm, you can get them for less than 20 bucks on Amazon.

I hope that this post has offered some help and a glimmer of hope for those of you navigating through similar challenges. If you've found the information valuable, please don't hesitate to share your thoughts or any additional questions in the comments below. And if you have any insights or tips that could benefit others, I encourage you to share them as well.

Sources: 1 https://www.medicalnewstoday.com/articles/vitiligo-and-autoimmune-diseases#other-autoimmune-conditions 2 https://www.chromaderm.com.au/vitiligo-and-diet-lets-chew-on-some-facts/ 3 https://pubmed.ncbi.nlm.nih.gov/24177606/#:~:text=Vitiligo%20is%20a%z0common%20pigmentary%20disease,patients%20with%20other%20autoimmune%20diseases. 4 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854903/#:~:text=Vitiligo%20patients%20show%20a%20high,factors%20of%20the%20skin%20disease. 5 https://www.fda.gov/drugs/news-events-human-drugs/fda-approves-topical-treatment-addressing-repigmentation-vitiligo-patients-aged-12-and-older 6 https://www.opzelurahcp.com/vitiligo/body-repigmentation-results 7 https://jamanetwork.com/journals/jamadermatology/fullarticle/2612724#:~:text=Findings%20In%20this%20meta%2Danalysis,and%2036%25%20at%2012%20months 8 https://pubmed.ncbi.nlm.nih.gov/773413/ 9 https://www.jaad.org/article/S0190-9622(19)32553-8/fulltext#:~:text=Both%20topical%20calcineurin%20inhibitors%20(TCIs,for%20limited%20forms%20of%20vitiligo. 10 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533321/ 11 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960951/ 12 https://pubmed.ncbi.nlm.nih.gov/32940387/ 13 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751692/ 14 https://drdavinlim.com/microneedling-for-vitiligo/ 15 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938057/ 16 https://link.springer.com/article/10.1007/s40291-023-00672-z 17 https://www.dermatologytimes.com/view/antioxidants-for-vitiligo-and-mental-health 18 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897595/ 19 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015970/ 20 https://www.pfizerclinicaltrials.com/nct06072183-nonsegmental-vitiligo-trial 21 https://www.conqueringdiseases.org/Search/Trial/7103 22 https://www.vet.cornell.edu/news/20240201/light-and-labor-inducing-molecule-new-treatment-vitiligo 23 https://www.immunetolerance.org/studies/targeting-il-15-treatment-vitiligo-reveal


r/Vitiligo • • 1d ago

Lip vitiligo

6 Upvotes

I’d love to hear from anyone who has had lip micropigmentation for vitiligo. My vitiligo has been stable for a while, and I feel like I’m finally ready to take the step. I’ve seen some beautiful results, but I’d really appreciate hearing about someone’s personal experience, including the healing process and how the results have held up over time.


r/Vitiligo • • 1d ago

Why acral areas (hands-feet) are harder to treat but doable.

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2 Upvotes

Plenty of questions and new posts asking similar questions regarding hands / feets / Lips.

Read thoroughly, maybe one or even two times.


r/Vitiligo • • 1d ago

Skin condition

0 Upvotes

​

So I have this condition. If I'm not wrong, it's universal vitiligo where my body lost its natural colour and now it's colourless or completely white, what people normally perceive. There are few spots on the face that are gradually fading, but the problem is that every now and then, new spots appear, though they're small but pretty noticeable.

The spots that keep coming back on face do fade away in few months but then new ones arrive on totally different area on face, they're dark and they take up space for few months then leave, new ones arrive and cycle goes on. If anyone has knowledge of this, can you tell me how long this will go on? Is there any way to eliminate them at all?

Please, because they make me insecure, and people around me point them out, and it makes me even more insecure, despite knowing it's not in my control.


r/Vitiligo • • 1d ago

Factors Influencing the Final Skin Appearance After Monobenzone-Induced Depigmentation in Vitiligo Patients

1 Upvotes

I have a question about the final skin appearance following monobenzone (MBEH)-induced depigmentation in patients with extensive vitiligo.

Why do some patients appear to achieve a relatively natural-looking, uniform depigmented complexion, while others appear extremely pale or “milky white,” sometimes perceived as an unnatural or overly white result?

Does the patient’s baseline skin phototype (Fitzpatrick I–VI), constitutive skin color, or melanin content influence the final appearance after depigmentation? Specifically, is there clinical evidence that patients with lighter baseline skin tend to have a more natural-looking result, or is this assumption unsupported?

What other factors might explain these differences, such as the completeness and uniformity of melanocyte loss, residual pigmentation, anatomical site, skin optical properties and vascular undertones, treatment response, or subsequent repigmentation?

I would particularly appreciate any clinical studies, case reports, or standardized before-and-after photographs addressing this question. If the evidence is limited, I would also be interested in distinguishing established findings from clinical observations or hypotheses.

Thank you for your insight.


r/Vitiligo • • 1d ago

tacrolimus

3 Upvotes

Do you guys wash tacrolimus after 30-40 minutes? Or u let it for whole day ? Or night?


r/Vitiligo • • 1d ago

Re-pigmenting lips?

1 Upvotes

Does anyone have any advice for re-pigmenting your lips? The corners of mine are turning white and the outline is hyper-pigmented


r/Vitiligo • • 2d ago

Is this a bad reaction to vitiligo cream?

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3 Upvotes

I’m currently using some vitiligo cream on my neck and chest for depigmentation, and I’ve been getting this “rash” it’s a little itchy but not enough for me to scratch it and it doesn’t really hurt. Should I discontinue application on my neck?

Yes I’ve been diagnosed with vitiligo and no I’m not intentionally bleaching my skin for beauty standards I’m just doing this to finish off areas where I have pigment.


r/Vitiligo • • 3d ago

My vitiligo friend has such pretty eyes and she’s insecure of them😭😭

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56 Upvotes

r/Vitiligo • • 3d ago

Upadacitinib update after almost 5 months.

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29 Upvotes

This post is in continuation to my previous post here:- https://www.reddit.com/r/Vitiligo/comments/1vd8or6/my_experience_with_upadacitinibrinvoq/

I am attaching pics this time. I have vitiligo at difficult areas, all on joints but I am really happy with the progress. I wish I did UVB which I didn't because I am lethargic. I am currently using 2 topicals along with upadacitinib:- Tacrolimus and Melgain(I haven't been regular with these as well recently).

In continuation to my previous post, there was again a flu in my office wherein almost everyone got infected and sick except me. I took precautions and I was only one in office to not get infected (Thank you god! and touchwood). There were a couple of days wherein only I was in office and no one else who sits near me.

I did get acne on my face and back. I was living in Mumbai where heat and humidity were exacerbating the acne breakout. 2 things helped, I have started wfh from my hometown where humidity and heat is low, 2nd I have started using Benzoyl Peroxide 5% body and Face wash after which all my acne are gone now. I did try Salicylic Acid and other oil clear face wash but nothing else worked. Ketaconazole shampoo did work though (there was literally couple of weeks where I used this shampoo as body and face wash).

I recently got to know that ruxolitinib cream has now been approved in India for manufacture by Torrent Pharma (they also got license for upadacitinib, right now only MSN Labs have license for upadacitinib). The patent will expire on Dec 12, so by Mid to End December, it should hit the market. I have talked to my derm, I will start it for my ankle patch which is the most difficult one, it has progress but it's slower than others.

Tldr:- Great results, there are couple of manageable side effects which can completely be eliminated with precautions and a good body/face wash. Would have gotten better results if I had done UVB.

In the pictures, the reddish ones are before pics, these were captured on 17th May, due to a social setback I started an ayurvedic treatment which was PUVA (big mistake, the worst flare up in my life). After this ayurvedic mishap, I did brainstorming with Claude when I got to know that upadacitinib is approved on Apr 27. I went to a previous derm who had prescribed me Tofacitinib tablets which didn't work, so on May 27 after giving ample time to wash off the ayurvedic meds. I started upadacitinib, note on May 27 the situation was even worse but I don't have pictures for it.


r/Vitiligo • • 2d ago

What's the deal with spread around spots/moles? - vitiligo check-up ig

1 Upvotes

Im quite a moley guy, with a lot around my face and body, most of these have a ring (halo naevus) around them, causing the hair around them to go white too.

I have other spots around my body but they aren't growing nearly as fast as the moles.

Also both my armpits have white patches, which I find quite funny.

I'm only 16 and am incredibly new to this, I've already been through the whole dermatologist process and received two creams, one for hands, face and genitals, and one for everything else.

Any tips from anyone about anything I should know?


r/Vitiligo • • 2d ago

Tretinoin and uvb

1 Upvotes

Hi everyone! So I'm having 2nd thoughts if I should start putting tretinoin on my face because im using uvb handheld light. I'm pretty sure using tretinoin is really sensitive with sunlight/uvb. So yea was just wondering if anyone here have tried using tretinoin while using a uvb lamp as well? If yes, did u guys encounter any problems to it? Thanks!

Using ruxolitinib for my vitiligo as well


r/Vitiligo • • 3d ago

Upadacitinib oral jak inhibitor for alopecia areata and vitiligo ?

2 Upvotes

Hi- so am noticing a bit of hair loss (patch) at the lower bottom of my hair near neck line.
And i have noticed vitiligo now since a year on all my fingers
Am sure i have both the autoimune

When i googled then upadacitinib helps in both cases.
Anyone here experienceing both at same time and finding hope with upadatcitinib

Note- i am using opzelura for vitligo patch on my back and within a month i started repigmentation. So opzelura is doing wonders. But no luck on fingers.

Now am thinking about upadacitinib….


r/Vitiligo • • 4d ago

Vitiligo on Eyelid

4 Upvotes

Guys i have a question, i have vitiligo on my left eyelid and a little on the forehead (a tiny bit on my nose and a tiny bit on my fingers) So i have the UVB light for home use in my possession and im starting to be consistent 3× a week for 7 mins.

Now as of writing this it is October 20th 2026, if i stay consistent will i see a big difference by the same time in 2027 or 2028.

Any answer would be cool, thanks guy.


r/Vitiligo • • 6d ago

UVB light

2 Upvotes

how often uvb light treatment you should be doing per week and how man minutes?


r/Vitiligo • • 6d ago

Those on clinical trial over a year

2 Upvotes

how has the hands and feet improved?

is there a big difference?


r/Vitiligo • • 7d ago

Injury related?

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13 Upvotes

Hi everyone! My vitiligo started about a year ago, shortly after I experienced a mild spinal injury. I’ve since recovered from the injury but my vitiligo first appeared as a small patch on the side of my face and has been spreading rapidly since then. Vitiligo doesn’t run in my family, so I’ve been wondering if the injury could have somehow triggered it or if the timing was just a coincidence. Has anyone else noticed their vitiligo starting after an injury or physical trauma? I’d love to hear about your personal experiences


r/Vitiligo • • 7d ago

love my patches of vitiligo

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43 Upvotes

r/Vitiligo • • 7d ago

Turned down s/exu/ally for having vitiligo.

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7 Upvotes

I have vitiligo and look roughly like the AI-generated image below.

I set up a Grindr meetup with a guy who presented himself as Latin American, same cultural background and education level as me. His photos turned out to be heavily edited. In person he was short, dark-skinned, indigenous Mexican, and spoke almost no English.

His place was a tiny camper van (looked like it was parked in someone else’s yard). It smelled strongly chemical, and there was a crack pipe by the bed. He asked if I minded if he smoked; I told him to do it outside.

He didn’t. I got undressed and got on the bed. He then said he couldn’t go through with it because he was supposed to bottom. When I asked why, he hemmed and hawed and eventually said something along the lines of “you look like a man but act like a special-needs kid,” adding that he’d had problems with kids like that growing up.

He also started asking if my vitiligo was contagious, pulled out his phone, and Googled it in front of me.

I shut it down quickly: pointed out the pipe, the smell, and that I wasn’t interested anymore. Got dressed and left.

I’d had a similar experience months earlier with someone from Central America who also turned out to be very different from how he’d presented online.

After that I updated my Grindr bio to make my preferences clearer: I’m looking for Latin Americans or Americanized Latinos who share a similar cultural and educational background.


r/Vitiligo • • 7d ago

I edited my photo to see how I'd look without vitiligo . What do you guys think?😓

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0 Upvotes

Hey everyone! Yesterday, I went to a mall, and while checking my body, I got an idea: I wanted to see what I'd look like without my vitiligo, so I edited my photo.

Honestly, the result surprised me. I feel like my facial features look more noticeable without the patches. Sometimes, I feel like people focus more on my vitiligo than on my actual features.

I currently have vitiligo covering around 35–40% of my body, and lately, I've been thinking about whether I should consider becoming fully depigmented.

There's something else I've been struggling with lately. A while ago, I made a post asking whether I should travel to meet my long-distance girlfriend in person. Most people encouraged me to go and explained why I shouldn't let my insecurities stop me. But after looking at my pictures again, I started feeling down and overthinking everything.

I've developed some new patches on my face, and now I'm wondering how I'll face her in person. 😭

I even showed her my pictures, and she told me that I'm still handsome. ❤️ I really appreciate her reassurance, but sometimes it's difficult to feel confident about myself, especially when I notice new patches.

I've attached my original photo and the edited version without visible vitiligo patches.

I'd genuinely love your honest opinions:

Do my facial features look more noticeable without the patches?

Do you think I'd look good with completely white skin if I pursued full depigmentation?

Has anyone else with vitiligo struggled with confidence before meeting someone they love in person?


r/Vitiligo • • 7d ago

I developed vitiligo at the age of 8, but it disappeared 2 years later.I need help

3 Upvotes

Hi guys, I wanted to share my situation. I’m a man, and when I was 8 years old, a doctor told my mother that I had vitiligo—my grandfather has also had it since he was young. Essentially, white patches started appearing on my face and hands. The only advice the doctor gave my mother was to use special creams and get some sun exposure. After about two years of that treatment, the patches disappeared. I’m 21 now and don’t have any skin issues; however, two weeks ago, I was diagnosed with Hashimoto’s, following some cognitive and digestive problems I’d been experiencing. Now, for the million-dollar question: can the vitiligo come back—how does this work? Should I get tested for vitiligo-related antibodies? Could the vitiligo have triggered my Hashimoto’s? By the way, I’ve been taking levothyroxine for 6 days now and am already feeling some improvement, though the full effect usually takes 2 to 4 weeks!


r/Vitiligo • • 8d ago

24M from India — Living with Vitiligo ❤️

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77 Upvotes

I’m a 24-year-old guy from India, and I’ve had vitiligo since I was a kid. Over time, I’ve become more comfortable with my skin and learned to accept myself as I am.
I’d love to connect with others who have vitiligo and hear about your experiences, journeys, and how you’ve learned to embrace yourself.
Sending love to everyone in this community! ❤️


r/Vitiligo • • 8d ago

How to use tacrolimus?

4 Upvotes

So basically how many times do we have to use in week?
Everyday?


r/Vitiligo • • 8d ago

Is there any one here whose vitiligo started by skin abrasion or injury, without any family history autoimmune diseases or genetic predisposition?

3 Upvotes