Denmark Stem Cell Clinic

I spent about an hour reviewing a Denmark based hair stem cell clinic with offices around Europe. What I saw was flamboyance with 8 start offices, some out of a castle, very impressive spokesperson, communicative in multiple languages including English, and lots of fluff. When it got down to the reality of what they were doing, it was FUE, plain and simple. It was a limited procedure that they demonstrated, and despite the claims that they were extracting stem cells and that one hair would produce two, and two would produce for and so on, the reality of what my professional eye was seeing was nothing more than a limited FUE procedure. I teach my patients a very basic principle about balding, that the buyer must beware of the con-artists that are always there to take you money.


2017-06-01 06:49:59Denmark Stem Cell Clinic

Post Finasteride Syndrome

It is not safe . I know a guy that took 3 pills and have been messed up for years. Check out a site called Propecia help and see the thousands of men there with horrific ongoing symptoms that have not went away even years after stopping this medication. I’ve read one guys post that says he would rather lose a limb than have post finasteride syndrome.

I have 25 years of experience prescribing finasteride so I know first hand what the risks have been. I have been managing finasteride with my patients and am always responsive when they develop side effects. I can’t explain why a man who took any drug that has a half life of 6 hours with just three pills, can have long term side effects, so I can’t help explain this to you.

Depression and finasteride

I have a history of severe depression. Will finasteride harm me?

With a history of depression, you need to discuss taking finasteride with your doctor. There are potential side effects with people who have a history of severe depression so great caution should be exercised when taking this drug and a close supervision of your doctor is important. I have written a post on this subject here: https://baldingblog.com/2017/05/23/finasteride-can-increase-depression-increase-actions-self-harm/

Poster on Reddit speaks out about Post Finasteride Syndrome (PRS)

My comments and opinions are really just meant to stand on their own merits or lack thereof. But I can share that I have had close visibility into what research the PFS Foundation has been doing over the past several years. Even once there is an important finding, it can take years before it makes it into the public eye. I wish things moved more quickly, but this is just the reality of research and the media. Just as an example, the legal documents that served as the basis for the Reuters story were (accidentally) filed publicly on the court docket in mid-2016, but it took over 3 years to make it into the mainstream media. The FDA has known about these issues since 2017 from the PFS Foundation’s Citizen Petition, but the FDA has done nothing yet. I hope the media will pick up on this but we will have to see.

The PFS Foundation has accomplished a few things so far:

Their research has established biomarkers in PFS patients. This shows that PFS is a physical condition rather than psychosomatic, as many people have argued for years. The studies looked at small groups of PFS patients and found two very important things. Compared to controls, PFS patients had undetectable (depleted) levels of neurosteroids in their CSF. Additonally, about 50% of PFS patients appear to have their 5AR2 gene silence. It would be great to have these studies done in much larger populations, but it is very hard to recruit PFS patients due to financial and logistical constraints when it is a rare disease. That doesn’t invalidate the findings of these studies of the existence of the disease itself.

Another Northwestern based study was a very high powered epidemiological study that showed about 1% of patients who took 5-AR inhibitors (finasteride and dutasteride) developed persistent erectile dysfunction. This was controlled in many ways using very sophisticated statistical techniques. Even at 1%, this is a low frequency risk but terribly significant if it occurs.

Lastly, a few years ago there was an article published in JAMA Dermatology that critiqued every one of the clinical trials to date that were published on finasteride. The main critique was that they were simply not effectively designed to sensitize for low frequency, persistent side effects. This article seems prescient now because Merck didn’t report the patients who dropped out of their study and there were apparently PFS patients within this group. This does not seem to have been an accident in retrospect in light of the documents that are now available.

Merck has acted unethically throughout this whole controversy. I can share with you a couple anecdotes with you.

Although I can’t specifically provide names, Merck has interfered with the research publishing process. Somebody from company reached out to at least one journal editor who published an unfavorable study on finasteride. Merck pressured them to withhold support to the journal if the editor did it again.

Personally, I had a physician reach out to Merck about a decade ago to figure out what was going on with my health. The physician spoke with a pharmacovigilance contact, but I don’t remember the name it was so long again. The person said Merck had never received any reports of sexual dysfunction. This was clearly false because of the data that was hidden from the clinical trials. Additionally, at that time Merck had already been forced to warn of such side effects in European countries. And this was shortly before the FDA forced a label change in 2012 to include post-marketing reports, all of which happened before my outreach to Merck.

These are all things I know factually to be true but I can’t provide “proof” until it gets into the public domain. I hope it gets there, but it may never be the case. But if you look at Merck’s response to Vioxx, they did many of the same things I just described for their response to the Propecia scandal.


2019-12-01 17:28:22Poster on Reddit speaks out about Post Finasteride Syndrome (PRS)

Determining Future Hair Loss

Hi Dr. Rassman. I am 22 years old but have been experiencing hair loss since I was 13. I have already tried Minoxidil (1 year) and Propecia (1 year) when I was 14-16 without stopping or slowing hairloss. I haven’t really lost much confidence due to my hairloss but it is very notorious now and would definitely like to do something about it. From what I can tell baldness comes from my dad’s side of the family (grandfather and father plus many of my dad’s cousins went bald) but no one has gone bald as young as I have. I think I am a class 3A Norwood and have been thinking about getting hair transplant surgery but I am worried if I will have enough of a donor area to cover the bald spot once the balding process stops, especially if I bald like my grandfather but so far it doesn’t seem to be the case. I was just wondering if at this advanced stage it was possible for a doctor to determine how much hair I will have left.

You need to have a good doctor define what is going on with your hair. Hair loss at 13 is rare, but can occur. If genetic balding has started that early, it would have been good to get a base line on the degree of miniaturization and the change over time. You must have that done now, before you get worse, or you will not know where your hair loss is going. With your history, a densitometry examination with quantification of the miniaturization in each area of your head will point to the long term pattern of your genetic hair loss (assuming that this is the correct diagnosis). There are other conditions as well, so it would be of great value to you to have a consult with someone like me, who is familiar with the causes of hair loss.

Transplantation in a person with certain conditions could be contraindicated. You need to be evaluated by a professional and even sending photographs will not give me the detailed microscopic examination I need. Please do not become your own doctor. This is not a game, but your future look we are talking about.


2005-07-20 12:43:00Determining Future Hair Loss

Press Release – Dr. Bernstein Improves Procedures Done with the FUE Robot

Snippet from the press release:

Robert M. Bernstein, M.D., F.A.A.D., A.B.H.R.S., a world-renowned hair transplant surgeon, presented a series of improvements to hair transplant procedures which use the ARTAS Robotic System for Follicular Unit Extraction (FUE). These updates include revisions to the FUE surgical protocol and technical adjustments to the robotic extraction system. He presented his refinements at the first user meeting held by the developers of the system; Restoration Robotics, Inc.; on September 14 – 16 in Denver, Colorado.

Dr. Bernstein described his series of improvements in a lecture to an elite group of physicians who are among the first adopters in the industry of the image-guided, robotic-assisted system.

Read the rest — Hair Restoration Pioneer Improves Robotic-assisted FUE Hair Transplant Procedures

For those doctors that use the FUE robot (ARTAS), these procedures that Dr. Bernstein presented should help to minimize problems with graft growth.

DHT Blocks Blood Flow to the Follicle?

From my understanding, hairloss comes from a variety of circumstances: genetics, nutrition, stress, etc. When it comes down to it, DHT blocks blood flow to the follicle, until the follicle eventually “dies.” Are there any products or studies being done to remove that blockage? If the blockage is removed, and blood flows back in, will the follicle grow hair again?

This is not an issue of blood flow to the follicle. Hair loss, when it occurs, reduces the demand for blood as the metabolic needs of the follicle are reduced when it becomes miniaturized. We know, for example, that if you put a normal hair follicle from the back of the head that has no genetic cause for its death, that hair will grow in the midst of thinning hair and when it grows it will be a thick, normal hair shaft. Your premise is incorrect, as DHT has little to do with blood flow directly.


2007-11-05 12:32:05DHT Blocks Blood Flow to the Follicle?

What is the problem curing curable diseases? Read below

Once upon a time, the world suffered.

In 1987, 20 million people across the world were plagued by a debilitating, painful and potentially blinding disease called river blindness. This parasitic infection caused pain, discomfort, severe itching, skin irritation and, ultimately, irreversible blindness, leaving men, women and children across Africa unable to work, care for their families and lead normal lives.

But the recent discovery of a drug called ivermectin was about to change it all. Not only was ivermectin cheap and easily synthesized, but it was also a powerful cure: With only one dose a year, it was possible to completely rid patients of disease and even halt the progression toward blindness. In short, ivermectin was a miracle drug – one whose discovery would lead to Satoshi Omura and William Campbell winning the Nobel Prize in medicine in 2015.

There was no time to be wasted. Recognizing that the populations most at risk of disease were those least able to afford treatment, Merck & Co. pledged to join the fight to end river blindness. Thirty years ago this October, the pharmaceutical company vowed that it would immediately begin distributing the drug free of charge, to any country that requested it, “for as long as needed.” It was the final piece of the puzzle: an effective drug for a tragic and completely preventable disease. And we all lived happily ever after.

Only… we didn’t.

Merck’s generous offer should have been the final chapter of a brief story with an upbeat ending – the eradication of a tragic and preventable disease that had plagued humankind for centuries. But such was not the case: 30 years later, in 2017, river blindness rages on across the world, afflicting as many as 37 million people, 270,000 of whom have been left permanently blind.

Neglected tropical diseases like river blindness stand in stark contrast to those like tuberculosis, which is estimated to affect a third of the world’s population due to the increasing prevalence of highly antibiotic resistant strains.

In short, tuberculosis has stuck around because medicine has run out of drugs with which to treat it – which is why, as a molecular biologist, I am researching new ways we can finally defeat this stubborn disease.

But this only increases the urgency for river blindness and other widespread diseases for which, unlike tuberculosis, science does have effective cures – and inexpensive ones at that. Even with all the necessary tools, the world has failed to cure the curable.

Turning a blind eye

One-and-a-half billion people across the world suffer from neglected tropical diseases, a group of infectious diseases that prevail in tropical and subtropical countries lacking good health care infrastructure and medical resources. These diseases typically do not kill immediately but instead blind and disable, leading to terrible suffering, creating losses of capital, worker productivity and economic growth.

Thirteen diseases are universally recognized as neglected tropical diseases. At least eight of these diseases, including river blindness, already have inexpensive, safe and effective treatments or interventions.

For less than 50 cents per person, the United States could cure a fifth of the world’s population of these severely debilitating and unnecessary diseases. In spite of this, the United States allocates nearly as little to treating and preventing neglected tropical diseases around the world as it does to drugs for erectile dysfunction.

The forgotten fevers

Consider dracunculiasis, or Guinea worm infection, which occurs when people consume water contaminated with fleas carrying parasitic worms. The worms mature and mate inside the human body, where they can grow to be two to three feet long.

Adult females eventually emerge from painful blisters at the extremities to lay eggs in stagnant water, where offspring will infect water fleas and begin the cycle anew.

No drug exists that can cure Guinea worm, but because of a cohort of mostly privately funded public health efforts, the number of Guinea worm infections worldwide has dropped from 3.5 million in the 1980s to only 25 in 2016.

Funding from the U.S. and other countries could help in the final push to eradication, and some argue that funding from the individual countries themselves could help.

Another example, albeit more grim, is the group of soil-transmitted helminths, or worms. Roundworm, hookworm and whipworm collectively affect over a billion people across the world, all in the poorest areas of the poorest countries. All these worms infect the human intestines and can cause severe iron deficiency, leading to increased mortality in pregnant women, infants and children. Furthermore, hookworm infections in children retard growth and mental development, leading to absences from school and dramatically reduced labor productivity.

However, soil-transmitted helminths can be expelled from the body with a single pill, each of which costs only one penny. What’s more, preventing infection in the first place is completely achievable through increased awareness and sanitation.

The purse strings of nationalism

Without drastic increases in funding and public awareness, the plight of people affected by the neglected tropical diseases is unlikely to budge anytime soon.

The U.S. spends over US$8,000 per person per year on health expenditures, compared to countries in Africa that spend around $10. While this opens the door to a critique on efficiency, it’s far more indicative of the disparities in health resources.

Less than 20 percent of the world’s population lives in some of the most developed and economically high-functioning countries, including the United States – and nearly 90 percent of the world’s total financial resources are devoted to the citizens of these nations. And yet, low-income countries bear the majority of the world’s infectious disease burden. In short, the rest of the world does not suffer the same diseases the United States does, and Americans are doing little to nothing about it.

At first glance, this is not so surprising. As a whole, the world suffers – but how many neglected tropical diseases currently penetrate American borders?

Some experts predict that eliminating or controlling the neglected tropical diseases in sub-Saharan Africa alone, which shoulders over 40 percent of the global burden of neglected tropical diseases, could save the world $52 billion and over 100 million years of life otherwise lost to disease.

Conversely, some global health experts estimate that for every dollar spent on neglected tropical disease control, we get back over $50 in increased economic productivity. By increasing awareness and funding of neglected tropical disease eradication, the United States will be making one of the best global investments possible. The rest of the world has waited long enough.

Katherine J. Wu, Ph.D. Candidate in Microbiology, Harvard University


2018-01-08 01:45:56What is the problem curing curable diseases? Read below

Did My Pain Pills Cause My Hair Loss?

i am 21 years old and i started loosing some of my hair when i was 19. It was all of the sudden after i had a kidney infection and was put on pain killers and cipro. it began to grow back until i got my wisdom teeth out which required me to be on pain pills for a month which caused significant hair loss. That was about a year ago and although i feel it doesnt fall out in the same large quantities i feel that the hair that has grown back is fine baby hairs. Is there anything that can reverse this or will i loose all my hair?

Physical stress and sickness are known causes of temporary hair loss, as are adverse drug reactions. That being said, pain pills are not a known cause of hair loss and are unlikely to be the reason your hair thinning orfalling out, so it may be a coincidence since when you were sick both times you had to take pain pills as part of your recovery. Therefore, the most likely cause of your hair loss is that the physical stress from your sicknesses caused the hair to have weak growth and/or shed.

Hair can take some time to recover, especially if your body is still recovering to full health – getting healthy is the best way to reverse this sort of loss. You may want to get evaluated by a dermatologist or a knowledgeable hair doctor to see if there is some component of genetic/pattern loss and get your hair mapped for miniaturization, but you should be reassured that it is unlikely you will permanently lose all your hair due to the events and medications you describe, unless you are amongst the unfortunate few who has hair shaft thickness changes early in life.

Propecia and Breast Milk

Hi Doc,

You are an impressive personality, I have been reading and making my decisions about my hair loss through the research on your website.

My wife is pregnant and and I want to start taking propecia, I am thinking about start taking it after the baby is born which is due on mid Nov. But I would like to know if breast feeding and propecia can create complications to the baby or wife. I think I am a norwood class 4 and have almost good coverage, I am 25 year old male.

Your reply would be a great help.

Keep up the great work.

Nope. Unless you have found a way to create milk from your own breast and are breastfeeding your baby, there is no danger to your wife and your baby as Propecia does not come over to the woman from sexual intercourse. It is not known if Propecia can be found in the breast milk of mothers that are taking Propecia themselves, but Propecia is not approved for use in women anyway. It will not affect your wife or unborn child even if you are having intercourse with your wife while she is pregnant. The pharmaceutical company Merck’s statement on this is, “Available data indicate that the level of PROPECIA in the semen of a man taking PROPECIA does not pose a risk to an unborn child. Accordingly, a man can take PROPECIA while conceiving a child with his partner, or have sexual intercourse with his partner if she is already pregnant.

If you are still worried, use a condom.