Dr. U Hair & Skin Clinic | FUE Hair Restoration, Dermatology and Laser Surgery | Los Angeles, Manhattan Beach | Dr Sanusi Umar MD

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This article describes one person’s experience and is not medical advice or evidence that a particular approach will work for others. Gashee products are not FDA approved to diagnose, treat, cure, or prevent disease. Consult a qualified healthcare professional about diagnosis and treatment decisions.

Video: Cheyenne on John’s Acne Keloidalis Nuchae and Losing Hope

Jason Thompson — Thu, 08 Oct 2026 23:31:43 +0000

For Cheyenne, watching John live with acne keloidalis nuchae meant witnessing changes she could not stop and questions she could not answer. In this chapter, she speaks about the frustration, the difficult treatment experiences, and the loss of hope that followed years of searching for help.

Watching the Changes Add Up

Asked what it was like to watch John go through his experience, Cheyenne answers plainly: “It was hard. It was really hard.” She recalls seeing gradual changes, depression, weight gain, and a growing sense that John was losing hope.

Her perspective adds another dimension to John’s account. The condition affected him directly, but Cheyenne also lived alongside the uncertainty, watching someone she loved struggle while trying to understand what might help.

Cheyenne reflects on how difficult it was to watch John struggle.

A Difficult Experience With Injections

Cheyenne remembers one especially frustrating period during John’s visits to doctors. She says that after injections, he experienced hiccups that continued for about a week. This was not an occasional hiccup that quickly passed, she explains, but something that seemed to go on without stopping.

She recalls John describing the experience as an allergic reaction to the injections and says he stopped receiving them. Her account describes what the couple experienced; it does not establish a medical cause for the hiccups or independently confirm an allergy.

For Cheyenne, this episode added to the feeling that John already had too much to deal with. Seeking answers had become difficult in its own right.

Supporting Someone Without Having the Answers

“It’s hard to see somebody that you love going through something so difficult,” Cheyenne says. She explains that she was not a doctor and did not have the answers he needed. When the conversation turns to feeling powerless, she agrees.

What she could offer was encouragement: supporting John and urging him to continue exploring treatment options. But encouragement did not erase the frustration of going from one doctor to another over roughly 20 years without finding the answers they were seeking.

Cheyenne discusses the long search for answers while images of the couple appear in the chapter.

When Years of Searching Wear Down Hope

Cheyenne describes those repeated appointments as a “revolving door.” Over time, she says, frustration set in and hope faded. She recalls a doctor telling them the condition would never go away.

The chapter does not resolve what comes next for John. Instead, it makes room for the experience of the person beside him: someone who saw the struggle up close and kept offering support even when she could not change the situation herself.

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Continue following John’s story in the next chapter.

Medical Disclaimer

This article shares a personal experience and is for informational purposes only. It is not a diagnosis or individualized medical advice. Consult a qualified healthcare professional about symptoms and treatment options.

Video: Marcus Describes Daily Pain From Acne Keloidalis Nuchae

Jason Thompson — Wed, 07 Oct 2026 17:31:25 +0000

In Chapter 6 of The Bumpinator, Marcus gives Dr. Sanusi Umar a direct account of what his scalp keloid feels like day to day. Beyond what can be seen, he describes pain at the highest point on the scale, frequent itching, and a past period of bloody discharge.

A Keloid That Has Grown Over Three Years

As Dr. Sanusi Umar examines Marcus, the conversation turns to the size of the keloid and the symptoms underneath it. Marcus says it has grown significantly over the past three years. The chapter then moves from appearance to the physical experience he is living with every day.

Dr. Sanusi Umar examines Marcus as their conversation turns to the symptoms associated with the scalp keloid.

“A 10” on the Pain Scale

When Dr. Umar asks Marcus to rate the pain on a scale of 1 to 10, Marcus answers simply: “A 10.” He adds, “Yeah, it hurts every day.”

The pain does not require a particular activity to begin. Marcus explains that he can be sitting down when it starts hurting. His description makes the symptom burden central to this chapter rather than treating the keloid only as something visible on the scalp.

Marcus says the area can hurt every day, even while he is simply sitting down.

Itching and Past Bloody Discharge

Marcus also reports that the area “itches a lot.” When Dr. Umar asks whether he gets bloody discharge, Marcus says that he has in the past and recalls one period when it continued for about a month.

For Dr. Umar, the examination and conversation bring the patient’s reported symptoms into focus alongside the visible growth. Marcus’s account makes clear that his concern is not limited to bumps on the back of the head. Pain, itching, and discharge are all part of what he describes experiencing.

Following Marcus Into the Next Chapter

Chapter 6 centers on listening closely to Marcus as he describes what the keloid has been like to live with. His 10-out-of-10 pain rating, daily discomfort, frequent itching, and history of bloody discharge establish the concerns Dr. Umar is evaluating as Marcus’s story continues.

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Medical Disclaimer

This article is for educational and informational purposes only and does not constitute medical advice, diagnosis, or treatment. Individual experiences and treatment needs vary. Consult a qualified medical professional for personal medical guidance.

Video: Hair Transplant Training Advances With Skin-Responsive FUE Technology

Jason Thompson — Tue, 06 Oct 2026 18:25:39 +0000

From Buenos Aires to Manhattan Beach, experienced surgeons joined Dr. Sanusi Umar for hands-on training focused on new skin-responsive, all-purpose FUE technology and its use across a range of hair restoration scenarios.

A Hands-On Exchange in Hair Transplant Practice

The visit brought accomplished hair transplant surgeons from Argentina to Manhattan Beach for practical training with Dr. Sanusi Umar. The visiting physicians already brought extensive surgical experience and leadership within an established clinic network across Latin America and Spain. The purpose of the session was not introductory education. It was an exchange among experienced clinicians centered on hands-on use of a newer FUE technology.

The training combined direct practice with advanced technical discussion. According to the approved video context, the session was designed to work across the full range of FUE scenarios, giving the visiting surgeons an opportunity to engage with the technology in a practical setting while exchanging expertise with Dr. Umar.

Dr. Sanusi Umar leads a hands-on training discussion with visiting physicians during their Manhattan Beach visit.

Learning a Skin-Responsive, All-Purpose FUE Technology

The short video centers on the physicians working with UGraft and reflecting on the technology after hands-on exposure. One visiting physician describes the device as “very intuitive” and says he believes it can help move forward the quality of what a surgeon can offer.

Another perspective in the video comes from more than 30 years of hair transplantation experience. After working with Dr. Umar’s device, the physician calls it “excellent” and says he believes UGraft can make it possible to reach more types of complex cases. Those comments reflect the visiting surgeons’ own impressions during this training session and are not presented as a guarantee of clinical outcomes.

Hands-on practice gives the visiting physicians direct experience with the FUE technology discussed during the training session.

Experienced Surgeons, Advanced Technical Discussion

The exchange highlights a specific kind of professional training: experienced hair restoration surgeons evaluating a new tool through practical use and discussion with the physician behind it. Dr. Umar’s role in the session is both technical and educational, guiding hands-on work with the technology while engaging colleagues who bring substantial experience of their own.

The video closes on that exchange of expertise rather than a patient outcome. More from the physicians’ visit is expected to follow, continuing the discussion around advanced FUE practice and technology.

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Medical Disclaimer

This article is for educational and informational purposes only and does not constitute medical advice. Individual evaluation and treatment should be personalized. No specific result is guaranteed.

Video: Mia’s Hair Loss and the Commitment of a Family That Kept Looking

Jason Thompson — Mon, 05 Oct 2026 17:36:13 +0000

For Mia’s family, hair loss became more than a medical concern. Her parents, Fernando and Blanca, kept traveling from Arizona as they looked for answers for their daughter. In this Baldcast chapter, Dr. Sanusi Umar reflects on what their persistence says about the effect a child’s hair loss can have on an entire family.

They Kept Making the Drive

Dr. Umar describes Fernando and Blanca as fighters because they did not limit their search to what was close to home. They repeatedly drove from Arizona as they continued looking for solutions for Mia.

“They didn’t give up,” Dr. Umar says. “They wanted the best for their daughter.”

Mia stands with her parents as Dr. Umar reflects on the family’s commitment to supporting her.

Commitment to Mia’s Happiness

The conversation also returns to a Disneyland experience that required another long drive from Arizona. Dr. Umar calls attention to the effort involved and to how committed Mia’s parents were to her happiness. He connects that persistence with the impact the hair loss had on the family.

The point is not that every family will follow the same path. It is that Mia’s parents continued asking questions and seeking help rather than simply accepting the first answer presented to them. Their actions became part of the story Dr. Umar wanted to recognize.

Dr. Umar discusses the persistence Mia’s family showed while continuing to seek answers for her.

When Things Turned for the Better

Near the end of the chapter, Dr. Umar notes that things had turned out better and reflects on how fulfilling that must feel after the family’s effort. The chapter does not turn that observation into a promise for anyone else. Mia’s story remains one patient’s experience, and evaluation and treatment should be individualized.

For parents concerned about a child’s hair loss, Mia’s story underscores the importance her family placed on continuing to seek an appropriate evaluation. Their persistence is the focus here, along with Dr. Umar’s recognition of the commitment behind it.

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Medical Disclaimer

This article describes one patient’s experience for educational purposes. Results can vary. Evaluation and treatment should be individualized. This content is not medical advice and does not replace consultation with a qualified medical professional.

Video: Lichen Planopilaris: The Pattern That Changed Eleojo’s View

Jason Thompson — Sun, 04 Oct 2026 23:49:46 +0000

Eleojo is a practicing pediatric surgeon, hair specialist, and hair transplant surgeon who also experienced lichen planopilaris, or LPP, as a patient. In this Baldcast chapter, she describes an early encounter with Dr. Sanusi Umar that began with skepticism and shifted when she noticed a pattern in her own symptoms.

From Physician to Patient With Lichen Planopilaris

Eleojo came to the conversation with extensive medical experience of her own. The chapter introduces her as a practicing pediatric surgeon from the United Kingdom, as well as a hair specialist and hair transplant surgeon. Yet her professional background did not remove the personal reality of being a patient with LPP.

Her first impression of Dr. U was direct: “Oh, what a cowboy.” The comment captures the skepticism she felt at the beginning. What followed, however, gave her a reason to look again at what she was experiencing.

Dr. Sanusi Umar examines Eleojo’s scalp during the Baldcast segment.

A Change She Could Track

Eleojo says that within 10 days, the itching she had been experiencing “just settled down.” She also says she did not believe it herself at first. When she stopped, the symptoms started again.

That sequence became important to her because it suggested a repeatable pattern in her own experience: the itching calmed down, then returned after she stopped. The chapter does not reveal the full treatment story or final outcome. Instead, it centers on the moment when her observation began to challenge her original impression.

Why the Pattern Mattered

For a physician who was also navigating her own hair loss diagnosis, noticing that pattern became a turning point in how she viewed the experience. Dr. U frames this as the beginning of a broader hair restoration story, saying that the journey is “about layering.” This chapter leaves that idea open for the next part of the conversation rather than moving ahead of the story.

Eleojo and Dr. Sanusi Umar together as her Baldcast story introduces the experience that changed her first impression.

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https://dru.com/hair-surgery-hair-loss-medication-services/

Medical Disclaimer

This article is for educational and informational purposes only and does not constitute medical advice, diagnosis, or treatment. Individual experiences and responses can vary. Consult a qualified healthcare professional for guidance about your own condition and treatment options.

Video: How Acne Keloidalis Nuchae Limits Juan’s Time With His Son

Jason Thompson — Sat, 03 Oct 2026 23:01:32 +0000

For Juan, acne keloidalis nuchae became more than something he could feel on the back of his head. What he first thought was a small pimple in his early twenties grew into a condition that, in his words, created “limitations” in the everyday moments he values as a husband and father.

What Started as a Small Bump

Juan introduces himself simply: a trucker, a father, a husband, and a provider. He remembers the beginning in his early twenties, when he could not see much at the back of his head and could mainly feel what seemed like a small pimple. “It just grew from there,” he says.

That memory gives context to the bumps on the back of the head that became part of a much larger personal story. In this chapter, Juan focuses less on appearance and more on how the condition changed the way he responds to physical closeness with the people he loves.

Juan describes the limitations he experiences while the chapter also shows a close view of the back of his head.

When Playtime Comes With Limits

Juan says his son likes to wrestle, and he likes wrestling with him. But when his son reaches for his hair or gets anywhere near the back of his head, Juan says he pulls away and creates distance. His wife describes a similar barrier, explaining that even a hug can become difficult because Juan worries that she may touch the area.

These are ordinary family interactions, which is exactly why they matter so much to him. The condition has introduced a boundary into moments that would otherwise be spontaneous.

The Moments Juan Does Not Want to Miss

Juan’s concern is also about time. There are things he can still do with his son now, including picking him up and playing with him. He knows his son will get older, and he does not want those opportunities to pass before he can fully take part in them.

“They need to happen now before he gets older,” Juan says, “and then I miss out on those moments.”

Juan sits with his young son as the chapter emphasizes the family moments he wants to experience while his son is still little.

This opening chapter centers Juan’s experience and the limitations he describes. His story continues in the next chapter of The Bumpinator.

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Watch The Bumpinator, Episode 8, Chapter 1:

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Medical Disclaimer

This article is for educational purposes only and does not provide medical advice. Individual cases and treatment needs vary. Consult a qualified medical professional for diagnosis and treatment recommendations.

Video: Kevin Gets Back on His Motorcycle After Dissecting Cellulitis Treatment

Jason Thompson — Fri, 02 Oct 2026 20:42:13 +0000

For Kevin, progress after treatment for dissecting cellulitis is connected to something he uses every day: his motorcycle helmet. During this Bumpinator follow-up, he tells Dr. Sanusi Umar that the helmet, jacket, and motorcycle boots are now the first things he grabs before heading to work.

A Daily Routine That Means More

Kevin arrives with what he calls a surprise. He explains that he works on his motorcycle throughout the day and uses the helmet Dr. Umar gave him every day. The helmet now protects his head as he goes about his routine.

“The first thing I grab is my helmet, my jacket, my motorcycle boots,” Kevin says as he describes getting ready for work.

Kevin wears his motorcycle helmet as Dr. Umar reflects on a goal Kevin had expressed when treatment began.

Dr. Umar Reviews Kevin’s Progress

Looking back at Kevin’s earlier pictures, Dr. Umar says he continues to be surprised by the improvement he sees. He then asks to take a closer look at Kevin’s scalp and hairline during the follow-up.

The chapter also returns to Kevin’s earlier treatment for painful scalp lumps and hair loss associated with dissecting cellulitis. The supplied caption notes that his care included surgical scalp intervention. In this follow-up, however, the focus is on what Kevin can do now and on the appearance of his tattooed hairline.

Earlier and later profile images of Kevin are shown as the chapter reflects on his progress after treatment.

Finding the Right Balance in a Tattooed Hairline

Dr. Umar explains that the challenge with a tattooed hairline is making it look natural rather than harsh. He says the goal is neither to overdo nor underdo the tattooing. After examining Kevin’s hairline, Dr. Umar says he is very happy with it, calling the balance “perfect.”

A Goal Kevin Wanted to Reach

Dr. Umar recalls that when treatment began, Kevin had identified things he wanted to be able to do again. One of them was wearing a helmet while riding his motorcycle. Now, Kevin says the helmet is part of his everyday work routine.

For this chapter, that return to routine is the central milestone. Kevin is able to wear his helmet and, as Dr. Umar puts it, “go about his life without too much concern.” The next chapter continues Kevin’s story.

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Medical Disclaimer

This article describes one patient’s experience. Results can vary, and evaluation and treatment should be individualized. This content is for educational purposes and is not a substitute for medical advice from a qualified healthcare professional.

Video: Mia’s Alopecia Story: Her Mom’s Message to Parents

Jason Thompson — Thu, 01 Oct 2026 20:47:15 +0000

For Mia’s family, alopecia has brought questions that other parents may recognize when a child begins losing hair. In this Baldcast chapter, Dr. Sanusi Umar asks Mia’s mom what she would say to parents who may feel scared or alone, and her answer centers on continuing to look for possibilities and holding on to hope.

What Mia’s Mom Wants Other Parents to Hear

Dr. Umar frames the conversation around families facing hair loss in a child around Mia’s age. He asks what Mia’s mom would tell parents who are watching their child lose hair and may feel frightened or isolated by the experience.

Her advice is practical and direct: “Look for more results, more experiences, more options.” She repeats the importance of having options rather than stopping after a single perspective.

Mia’s mom reflects on what she would tell other parents whose child is losing hair.

“Don’t Give Up. There’s Still Hope.”

The conversation ends with the clearest part of her message. Mia’s mom tells parents, “Don’t give up,” and adds, “There’s still hope.” The chapter does not promise a particular result. Instead, it presents one family’s perspective for other parents who may be searching for answers and individualized care.

The accompanying caption places the discussion in the context of pediatric alopecia areata or alopecia totalis. It also emphasizes that this is one family’s experience and that results can vary.

Dr. Sanusi Umar asks what parents may need to hear when a child is experiencing hair loss.

Keep Looking for Answers

Mia’s mom does not tell families that there is one path they must follow. Her message is to keep looking at results, experiences, and options. For parents considering approaches such as non-surgical hair restoration or a hair growth treatment, the chapter’s emphasis remains on not giving up and seeking individualized evaluation rather than assuming one family’s experience will be the same as another’s.

The story continues in the next chapter of Mia’s Baldcast experience.

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Medical Disclaimer

This content is for educational and informational purposes only and is not medical advice. Individual experiences and results vary. Evaluation and treatment should be individualized by a qualified medical professional.

Video: Marcus and the Challenge of Severe Keloid Removal

Jason Thompson — Thu, 01 Oct 2026 19:47:15 +0000

For Marcus, the treatment discussion reaches a difficult point: what happens when a keloid has become too large for steroid injections to flatten it? In this Baldcast chapter, Dr. Sanusi Umar explains that removal itself is only part of the problem. The larger challenge is reducing the risk that the keloid returns after surgery.

When Steroid Injections May Not Be Enough

Dr. Umar explains that when keloids reach the size shown in Marcus’s case, steroid injections are not expected to flatten them. At that stage, he says surgery is required. The discussion places the size of the keloid at the center of the treatment decision rather than presenting injections as a solution for every case.

Dr. Sanusi Umar discusses the treatment challenge presented by Marcus’s large scalp keloid.

Removal Is Only One Part of Keloid Surgery

Dr. Umar says the central problem with keloids is not simply removing them. He notes that tissue can be removed using different surgical methods, including a knife or scalpel, electrocautery, or laser. The more difficult issue comes afterward: preventing the keloid from coming back.

That distinction matters in a severe case. The procedure can address the existing growth, but Dr. Umar emphasizes that recurrence is the major challenge that must be considered when planning treatment.

The chapter connects severe keloid removal with the surgical planning needed when injections are no longer enough.

Why Recurrence Can Make Surgeons Hesitate

According to Dr. Umar, the difficulty of preventing recurrence is why many surgeons may not want to take on a patient with a keloid of this severity. His explanation shifts the question from whether the growth can be cut away to how the case should be managed with recurrence in mind.

For people dealing with a Keloid or bumps on the back of the head, this chapter illustrates why evaluation and treatment planning need to account for the individual case. It does not show Marcus’s later outcome or make a prediction about what happens next.

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