Women with hypermobile Ehlers-Danlos syndrome are reporting change in symptoms they were told they would have for the rest of their lives, after finally addressing a tissue no hEDS prescription has ever been designed to touch.

Before any of the research, a word about why this page is in the first person.
I was diagnosed with hypermobile Ehlers-Danlos syndrome in 2012, at fifteen, by the fourth consultant I was sent to. The seven years before were appointments about separate things. A knee. A wrist. A jaw. A stomach. I was told, more than once, that I was a bendy girl who had read too much.
I stopped dancing at sixteen. I gave up the choir two years later, because holding a note upright for four minutes stopped being something I could do. In my second year at university I came home and finished the degree from my parents' front room. I had the name by then, and the name changed none of those three things.
I went into medicine with the diagnosis already in my own notes, and I chose this specialty on purpose.
What I had not expected was the vocabulary from the other side of the desk. None of it is in the literature. Bendy. Dramatic. Growing pains. One of the hypermobile anxious ones.
And what I had to put against it was the list I had been handed myself. Paracetamol. Naproxen. Codeine when the naproxen stopped covering it. A pain clinic letter with a waiting list attached.
That is finally changing, and not because of a new drug. Somebody put an ultrasound on a tissue nobody had thought to look at, in people with this diagnosis.
A research group put an ultrasound probe on the outer thigh, over the band of connective tissue running from hip to knee, and filmed it while the leg moved. Nine people. Some with hEDS, some with lower limb pain, some with neither.
It was not measuring how far a joint would bend. It was measuring how far the layers of that tissue travel across one another.
In the hEDS group the layers travelled 46.2 per cent.
In the people with neither pain nor hEDS, 121.1 per cent.
That is a tissue no rheumatologist examines in a normal appointment, and one no hEDS prescription was designed to affect.
It is called fascia.
It was the list I had been handed myself, at fifteen.
It is the connective tissue that runs through the body as one continuous layer, directly under the skin, wrapping every muscle, with pain nerves running through it in large numbers.
It has never come up in an appointment because for most of the last century it was the thing medical students were told to peel off the muscle and throw away.
The genetic panel could not have found it either. There is no genetic test for hEDS; that panel was ordered to rule out what this is not. The blood test was never looking for this.
It is not one sheet but several, stacked, moving across one another every time the body moves. What they slide on is a film of water held in place by one long molecule. Hyaluronan.
Anyone who has washed up knows the feeling. Two wet plates slide. Let the water go and the same two plates grip.
Once the tissue is in the picture, the symptoms stop looking like a list of unrelated complaints. Not as a dozen separate problems. As one problem, showing up in a dozen places.
Same probe. Same strip of tissue. A little over a third of the travel.
The answer here is not an event, which is the part most appointments skip over.
hEDS is in the matrix from the start. Researchers took skin cells from twenty women with the diagnosis, read every gene those cells were switching on, and found the machinery that builds connective tissue out of step across the board.
She was told that the growth spurt, the pregnancy, the operation and the long illness she privately dates it all from were coincidences.
None of those years caused this. What they did was load a matrix already being built differently.
The direction of the measurements is not the one most people assume either. In hEDS the fascia and the muscle under it have been described as abnormally soft, not tight. What has been measured is not a tissue pulling harder. It is layers that barely travel across one another.
Nobody knows yet why they travel so little. The measurement exists and the explanation does not.

On the left, the stacked sheets that wrap every muscle are travelling a little over a third as far across one another as they do in people without this diagnosis. That is the shoulder that leaves while a coat goes on, the rib that slips at a desk, and the waistband still being felt at nine at night. On the right, the same sheets with the film of water between them doing its job.
Paracetamol and naproxen are painkillers. Codeine is an opioid. Amitriptyline, where it is offered, is an antidepressant at a low dose at night. All of them turn the volume down on a signal.
None of them goes near the tissue producing it. The layers are still travelling less than half as far, and the nerves running through them are still being pressed on. The medication lowers the alarm and leaves the fire.
Then the physiotherapy she has probably not been three months without. It is aimed at the joint. Stronger muscles around a joint that has stopped holding itself is worth having, and it is a different target entirely.
Then her own shelf. Magnesium, aimed at cramp and sleep. Collagen, aimed at the fibre, a different part of the same tissue. Vitamin C, which rests on one 2005 hypothesis paper about a different type of EDS and has never been tested in anybody.
And a bottle of hyaluronic acid serum, because if it says hyaluronic acid on the side she has already bought this exact material once. A molecule has to be under about 500 daltons to cross skin, and hyaluronan is orders of magnitude over that line. It stayed on the outside of a shoulder.
Which leaves one route anybody has tried. Swallowed, bacteria in the gut cut the long chain into fragments small enough to absorb. Not through the skin. Through the middle.
Hydraform Fascial Release is that material and nothing else. 150 mg of hyaluronan a day in two capsules, with the manganese the body uses when it builds connective tissue. Manganese contributes to the normal formation of connective tissue.
It is not a painkiller, not an antidepressant and not an opioid. It numbs nothing.
Fascial Release
150 mg hyaluronan with manganese. Two capsules a day. Ninety days to judge it.
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2-Pack + 2 Free Gifts
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What there is not, and this page will not pretend otherwise, is a clinical trial of this material in hEDS. Nothing swallowed has ever been trialled in this condition at all.
Three further limits belong here rather than scattered through the page. The glide measurement is nine subjects at one site. The group describing fascia this way is small, and it wrote both those measurements and the review that gathers them. And the hyaluronan step is borrowed from fascia research in general, because hyaluronan has never been measured in hEDS fascia.
What there is, is the people already taking it.
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324
clinicians share it on FrontrowMD, uncompensated
150mg
hyaluronan a day, in the range swallowed-hyaluronan trials have used
90
days to judge it, with every penny back if it does nothing
Hyaluronan, 150 mg a day. The material the sliding layers run on, and the only thing here aimed at travel rather than at the fibre, the joint or the signal. No amount of drinking water puts a film of water between two sheets. This is the molecule that holds it there.
Manganese. The mineral the body uses when it builds connective tissue, and the one ingredient here carrying a claim anybody is formally entitled to make.
No painkiller. No antidepressant. No collagen, which is the fibre, and no vitamin C stack.
Vegan, third-party tested, made in a GMP-certified facility, sixty capsules to a pouch.
Nothing needs to be stopped in order to start. It contains no painkiller, no antidepressant and no stimulant, so there is nothing to come off first.
It has not been formally tested alongside naproxen, codeine or amitriptyline, so it is worth a word with a doctor or pharmacist, particularly alongside a blood thinner. Nothing here is a reason to change a prescription or to stand the physiotherapy down.
Two capsules a day with water, with food or without. Nothing to time, nothing to log.
Timing matters here more than most people realise, and not for any reason to do with stock or a deadline.
A sliding surface that has been doing a fraction of its travel since childhood has been loaded that way for every one of those years, and nothing about that changes on its own.
Which means the state the tissue is in today is the easiest it will ever be to supply.
And nothing happens in week one. Connective tissue turns over slowly, and anything promising a result by a particular date is selling the date.

Take it for the full ninety days and judge it on one job: carrying the shopping in from the car without a shoulder going. If that is no different at the end of it, you get every penny back.
Nothing to post. No form. No conditions. Ninety days because that is how long this tissue takes.
Everything above is what the research says. What follows is what three women who found it on their own have written, and nobody told them what to look for.
Fewer of the small daily dislocations
Keeley M. · ★★★★★ · Verified purchase
Everyone focuses on the big subluxations but it is the small constant ones that wear you down
Fingers, jaw, ribs. I have been taking these since February. The splints are still in the drawer but I reach for them less than I did, and the all over ache the day after a busy day is not what it was.
The morning stiffness is the part that shifted
Aisling D. · ★★★★★ · Verified purchase
I expected nothing because nothing else has worked
What changed was the first hour of the day. I used to need a long time before I could grip anything properly. That hour is shorter now. I notice it most on cold mornings.
It has not fixed my joints and I did not expect it to
Robyn P. · ★★★★★ · Verified purchase
Being honest, my hypermobility is exactly the same, it was always going to be
What is different is the soreness in between the joints, the bits nobody can point at on a scan. That has eased enough that I have stopped bracing myself before I get out of a chair.
No. This contains no painkiller, no antidepressant and no stimulant, so there is nothing to come off first. It has not been formally tested alongside naproxen, codeine or amitriptyline, so check with your doctor or pharmacist, particularly alongside a blood thinner. Nothing here is a reason to change a prescription.
Same material, and that is exactly why the serum did nothing for a joint. A molecule has to be under roughly 500 daltons to cross intact skin, and hyaluronan is orders of magnitude larger. It was aimed at the outside of a shoulder and stayed there.
Nobody can honestly tell you that, because no trial of this material has been run in hEDS and nothing swallowed has been trialled in hEDS at all. What can be said is that fascial layers in hEDS have been measured travelling less than half as far as in people without it, that those layers slide on this material, and that nothing else has been aimed there.
No. Collagen is the fibre in connective tissue. This is the material the layers of it slide on. The nearest real trial of collagen peptides improved how stable people said their ankle felt and found no difference on the instrument that measured it.
Because connective tissue turns over slowly and thirty days is not a fair test of it. A thirty day guarantee on something like this runs out before the question can be answered.
Ninety days from the day it arrives, every penny back. Nothing to post, no form to fill in, no reason to give. Keep the pouch.
I was told for seven years that there was nothing to find, and the panel that finally got me the diagnosis was ordered to rule out everything this is not. There is still no test that finds it.
That is not an answer anybody can hand back now. It is the reason this page exists.
Fascial Release
150 mg hyaluronan with manganese. Two capsules a day. Ninety days to judge it.
1-Pack
2-Pack + 2 Free Gifts
3-Pack + 3 Free Gifts
★★★★★ Rated 4.8 from 1,700+ reviews