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Managing Ehlers-Danlos syndrome: a physician's perspective 

Te Tāhū Hauora Health Quality & Safety Commission
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This video is part of a series about a rare condition called Ehlers-Danlos syndrome, and how working as a multidisciplinary team can improve patient outcomes. The videos include interviews with a consumer, Tracey, and members of the multidisciplinary team that help to manage her condition. In this video, Dr Fraser Burling speaks about his experience working as a dual physician and rheumatologist in a multidisciplinary team to improve health outcomes for patients, including Tracey.
An international expert opinion was received on the treatment described in these videos. Download a copy of the opinion, written by Dr David Rabago from Penn State College of Medicine: www.hqsc.govt.nz/assets/Consu...
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This series of videos describe the experience and treatment of one consumer with Ehlers-Danlos Syndrome (EDS). Three members of the multidisciplinary team (MDT) involved in the care and treatment of this person are interviewed.
We acknowledge that a MDT can be much larger than this and the video does refer to the wider MDT as an important aspect of diagnosis, treatment and care of people with EDS.
Owing to the diverse and complex presentation of EDS, Rare Disorders NZ (formerly NZORD) has produced guidance (funded by the Ministry of Health) that will help health care professionals and providers to assess, diagnose and plan care for people with EDS.
Such guidance will hopefully promote discussion amongst health providers treating EDS, resulting in improved care and outcomes for consumers.
ACC sourced expert opinion about the evidence-base of prolotherapy being provided by Dr Burling. This expert opinion stated, “Clearly there is support for this in the literature.”
www.hqsc.govt.nz/assets/Consu...
At an ACC review hearing, the reviewer considered this treatment had been excluded from the ACC prolotherapy assessment and that it was “a generally accepted means of treatment within New Zealand.” As such, ACC paid the cost of prolotherapy for the consumer during the entire rehabilitation programme. The prolotherapy treatment described by Tracey has had positive results for her.
There is mention throughout the videos of the prevalence of EDS and indication that this is varied; prevalence will depend upon the definition being used and this will determine the inclusion criteria.

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20 янв 2021

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Комментарии : 136   
@alecbrown66
@alecbrown66 7 месяцев назад
I have had eds/hms for over 40yrs, and so much stuff hits us out of nowhere, that frankly the patient becomes more expert. I would love to see a doctor or consultant who suffers from chronic eds/hms,,and let them experience the daily hell it is and the ignorance and cynism so many doctors treat us with.
@jackiemiles1091
@jackiemiles1091 2 года назад
I was suicidal before my diagnosis and treatment plan. I had no hope. Getting the diagnosis and having doctors take me serious gave me hope and a reason to live again.
@mikatricktricken
@mikatricktricken 2 года назад
Do you have type III would you be intrested in talking?
@Rls_0523
@Rls_0523 2 года назад
That's where I am right now. Was there any treatment that pulled you out of it, or just the diagnosis and doctors that gave you hope again?
@mikatricktricken
@mikatricktricken 2 года назад
I live in the states and i haven't found a good multicare facility yet... frustrating
@carterfamilyfuntime1705
@carterfamilyfuntime1705 2 года назад
It took me 9 years to find what was wrong with my body. I was very suicidal thinking dying would be better than living this way. I had several doctors tell me its in my head what im feeling isnt possible that i need a psychiatrist or treated me like I was drug seeking. Which I have been in recovery for for about 15 years methadone treatment and have only been taking my prescription for 15years. Im managed. So finally i found a distant relative who had it posted on her Facebook page and i read the symptoms and knew right away that is whats wrong. I still haven't been diagnosed but i know its what is wrong. I can't find a doctor that will listen to me or take me seriously. Its terrible
@bestoonisa9007
@bestoonisa9007 2 года назад
you can get completely cured.
@ajohnson3830
@ajohnson3830 10 месяцев назад
For 30 years no doctor has ever been able to give me a diagnosis. I’ve lived in severe pain for years. Barely able to walk, lost my job and have had 8 orthopedic surgeries. I was however kicked out of the Army in 1981 for EDS.
@joshprice32000
@joshprice32000 Год назад
My stepdaughter was just diagnosed with EDS after years of trying to figure out what was going on with her. So glad there is treatment and things we can do!
@mikatricktricken
@mikatricktricken 2 года назад
Hearing him at 4:00 made me tear up. My pain is so unmanaged and I'm starting to give up hope. Knowing this is progressive is making me give up... but hearing i could get back to a life again just gave me so much hope and happiness
@gouachepottwo7537
@gouachepottwo7537 2 года назад
This. This is how I felt hearing this I'm 22 and I just want to live. I didn't know about the eds till around 2 years agoish its gotten much worse and hearing him say that is fucking awesome.
@melissastory1993
@melissastory1993 2 года назад
Me too!
@shannongreenwell1278
@shannongreenwell1278 Год назад
I have read that it is a progressive illness but I have to keep holding onto my faith! I have done research on it as soon as I saw my diagnosis on paper.
@LadyInWhite741
@LadyInWhite741 Год назад
Have you ever heard of taking Low Dose Naltrexone for pain? (Non opioid) It has helped my hEDS significantly! I’m currently on 3mg. I’d say from 1-10, my pain was at a 8-9 most days and now it’s at a manageable 3-4. You will still have flare ups and bad days, but the medication on a day to day basis really has made such a drastic difference in my anxiety and mental health all around too.
@shannongreenwell1278
@shannongreenwell1278 Год назад
@@LadyInWhite741 I have to be careful with what I take, I have such high allergies to so many other medications, plus I have Epilepsy also along with my EDS.
@kat-nd3un
@kat-nd3un 2 года назад
Thank you for posting. Fraser has saved my life. I would not be here without him, he is an amazing person and I owe him everything.
@onefabknitternz
@onefabknitternz 2 года назад
I am on the waiting list , looking forward to getting some real help !
@jennadee6761
@jennadee6761 2 года назад
I wish there was a doctor like this in Australia! 🥺
@confusedman423
@confusedman423 2 года назад
@@onefabknitternz same!!
@anyalazor7978
@anyalazor7978 Год назад
Hi, Courtney! I have EDS and severe pain too, I can barely stand up at all. Can I ask, did prolotherapy injections help you with spinal instability? Or is this treatment mainly aimed at muscle pain? I was told I might need a long spinal fusion which I really want to avoid but I don't know if prolotherapy can help with instability or only muscle pain. Thank you!
@josiefaber9314
@josiefaber9314 Год назад
@@anyalazor7978 Fraser’s prolotherapy has helped my spine / it’s been a long, slow process but it’s been remarkable
@AlisonCurry
@AlisonCurry Год назад
No one in my city will give me a treatment plan, all the rheumatologists reject me due to EDS... MY hand joints are so awful now and my movement and hypermobility. Idk why no one will help.
@patriciagriffin1505
@patriciagriffin1505 2 месяца назад
Ignorance
@cynthiabemis2959
@cynthiabemis2959 10 месяцев назад
My oldest son had ehlers danlos syndrome he had the worst kind and was hospitalized most of his life in and out of the hospital he passed away at the age of 33 . I was told that the eds is passed down from my mothers side and
@Spanglefangle
@Spanglefangle 10 месяцев назад
We also have larger amygdalas generally and more reactive flight or fight systems.
@shannongreenwell1278
@shannongreenwell1278 Год назад
I have EDS and mine is the Classical type, mine is type two. I can do the splits as a child and I still can. I can stretch my shin on my hands, under my eyes and on my neck behind my ears. I live in constant excruciating chronic pain! I bruise easy and I fell at my work and it took me a while to heal and I still will trip when I am walking thus I rely on my cane to help with stability. I got my diagnosis from my Neurologist, because I, too have Epilepsy. But my Epilepsy is not due to my EDS. I am now being tested for POTS or another form of Tachycardia. I use a Wheelchair or a Rolling Walker at my church because the building is very big and by the time I get to the church sanctuary I would be in pain and out of energy as well as lightheaded and unable to enjoy the service and the sermon. My EDS has progressed in my vision, thus is why my eye doctor is keeping a close watch on my eyes.
@Lee-iq7wg
@Lee-iq7wg Год назад
In primary school i use to lie on my tummy and put legs over my head all the way up to my calf 😬 Prior to surgery I could stand with both feet facing backwards 😅 Lest I forget the tree climbing version of "chicken".. who could jump from the highest branch. My advantage came in when I landed from great heights and my joints would dislocate.. I'd just pop em back in!! circus freak hours over here .. Have totally tried to off myself many times yikes. I feel so bad for my GPS over the years, they have to manage so many patients and so many different conditions. They never know about EDS but do their best. Def heading back into suicidal territory as I age and things keep getting worse uhg. I just want to be able to work, use my hands properly, and find someone who can help with ehlersdanlos without it costing thousands of my nonexistent money.
@Ana.Forlin
@Ana.Forlin Год назад
I wish you were in Atlantic Canada. I just want to stop living in pain and misery and being told that there's nothing wrong with me, but never having an explanation as to why my body is doing all these weird things it's doing.
@roebbiej
@roebbiej 2 года назад
Thank you do much.
@kimtonearts
@kimtonearts Год назад
Good info, Thank you for helping ppl w/ EDS.
@amyamy07
@amyamy07 6 месяцев назад
I was born in Timaru 1963. Always had hyper 8:24 joint mobility. I am still having a hard time with Doctors in Australia. I live in Darwin now.
@ooulalah4333
@ooulalah4333 Год назад
This was very helpful
@lemonbade
@lemonbade Год назад
I feel like I’m getting worse every day and have no help from GPs here in UK.
@Rls_0523
@Rls_0523 2 года назад
I feel like I'm too sick in too many ways to be helped. It's very unfortunate that the links listed here go to link not found results. I was hopeful I could give that information to my doctors and maybe get some relief. They've put me on depression and anxiety meds and have already increased them, within a year, but there's been no improvement. The reason for this is severe pain and poor quality of life are the cause of my depression and anxiety, but my pain meds haven't been changed or increased since I started them >20 years ago. I've lost almost all hope of getting real help. I don't know what else to do and wish doctor assisted compassionate end of life were rights for every person. We shouldn't have to contemplate some violent suicide, when we could go peacefully and humanely with our loved ones around us instead. I'll never understand how it's the humane thing to do for animals, but not for humans.
@carterfamilyfuntime1705
@carterfamilyfuntime1705 2 года назад
Ive had the same thoughts myself. I have been struggling for 10 years and just finally figured out what my condition is last year because a distant relative has it. I was doing my family tree and a family member had posts on Facebook about it. I still haven't gotten diagnosed yet i cant find a doctor who will take me seriously and believe me. Or even listen to me for 5 minutes. In the beginning when my baby broke my nose with his head throwing his head back i started feeling everything in my face moving around then it traveled through my entire body everything moves underneath. Try to explain this to an emergency room doctor. They gave me a catscan xray but only said theres nothing wrong and it is in my head. Its not possible. I wonder if they ever figured out that it is possible and that had they treated me sooner ot might not be as bad as it is. My family doesn't understand what im going through. I try to talk About what im feeling and i get treated like im crazy. So i suffer in silence with it. When are they going to actually believe me when I drop dead from organ rupture? Or kill myself because the pain is too much to bare. Idk. Having someone to talk to that gets it might actually help me at least i wont feel like im all alone in this world with something that i thought no one else had for like years.
@whoswhoo
@whoswhoo Год назад
He mentions drugs he uses to control pain you must get on them .pain causes depression anti depressants don't help pain relief is what works you've a right to better treatment look for a specialist get referred it's easy to fell hopeless from chronic pain .
@Rls_0523
@Rls_0523 Год назад
@@carterfamilyfuntime1705 I'm sorry you're suffering. Unfortunately, I've found even having the correct diagnosis doesn't always make a difference. I finally have the correct diagnosis, but it's something the ER staff hasn't heard of, so they treat me like I'm stupid, drug seeking (even though I'm asking for anaphylaxis treatment, not pain meds), or both. I had a nurse refuse to give me epinephrine, as the Dr ordered, because it "wasn't anaphylaxis like she'd seen before". She told her boss it didn't make sense to her and I was stupid. I told her, not all anaphylaxis is caused by a food allergy and I would expect a nurse of any experience to know that. Her boss called me to get more details and I told her that nurse has no place working in an ER. She needs to work in an office where they see the same shit every day and it's not life or death, at least until she gets more experience. There's nothing I hate more in the medical field than a know it all that doesn't know much and looks down on their patients because they don't have all the answers. I'm fed up with having to pay for no help and incompetence. It should be like hiring a plumber, if they don't fix anything, you don't pay.
@MsMesem
@MsMesem 8 месяцев назад
Misogynie@@Rls_0523
@mavr1215
@mavr1215 9 месяцев назад
I recently tripped over and dislocated my shoulder. So much pain 😢
@donnacostarella4241
@donnacostarella4241 3 месяца назад
This disorder affects the whole body and yes we get depressed it’s never ending too. Also Thank You to the dam vax everything escalated in flare since 3 dam years now pissed off is saying it mildly. Now compressions to deal with too besides the other issues we have grrrr
@viviengiannacaple-chuley4408
@viviengiannacaple-chuley4408 8 месяцев назад
Hurrah for realising we are so many.
@theangrytiredzebra
@theangrytiredzebra 6 месяцев назад
Omg i wish i could be made pain free. Im wheelchair bound and drowning in overwhelming pain. I also have Syringomyelia and loads of comorbid conditions. No help here in Oklahoma
@patriciagriffin1505
@patriciagriffin1505 2 месяца назад
Yes help not as available in US as other countries
@alanwhite-zv5ii
@alanwhite-zv5ii Год назад
My wife was recently diagnosed by her genetics Dr. Only problem is all the Dr's at Kaiser will not recognize disorder and don't have a treatment plan or listen to any suggestions. It is still in there eyes only in her head.
@HeartOfTheSource
@HeartOfTheSource Год назад
Hi, what are the treatment options? My new Rheumatologist had just connected the dots on this with all my life long symptoms as for the being "double jointed" and palms flat on floor while legs straight thing, my yoga teachers were amazed and also the velvety soft skin people that hug me always say something like "you are so soft! Or you don't feel real". Traits most people seem to admire, yet now thinking they were symptoms all along . I'm overly sensitive to many medications. Side effects almost killed me so no more experiments. Was prescribed up to 18 medications at one time....Are there specific supplements needed? I've had POTS and vertigo since I was 2 years old, my parents disregarded it as me being sensitive to the environment. One of my children is also showing similar symptoms, also my youngest sister has had issues all her life too. I was misdiagnosed with Lupus even though all lupus tests showed negative so that was finally dismissed as a cause. Been in terrible pain and getting worse 😢 Is there really any hope that's going to be affordable? I'm currently disabled but fighting. I keep trying to make work attempts. Advice needed. Thank you.
@hoosier2003
@hoosier2003 Год назад
Are you in the states?
@youknowtherules8888
@youknowtherules8888 Год назад
I was really healthy a few months ago. I took some food supplements and my body reacted badly. My hips and joints feel like they are breaking all the time. I’m almost completely crippled and just want my life back.
@Bendylife
@Bendylife Год назад
My doctor just diagnosed me, bit I have no treatment plan. I was told in BC canada there is nothing available to help people with EDS. Super lost at this point.
@loriboyce942
@loriboyce942 Год назад
We're in Alberta and told the same thing.
@MsMesem
@MsMesem 8 месяцев назад
There is not much real help ANYWHERE. In France the doctors most active in research have retired.
@KW-ks7ih
@KW-ks7ih Год назад
I need more info about this treatment. Anyone here with first hand experience? My shoulders dislocate on a weekly basis with daily spasms. I had a doctor when i was a teenager incorrectly diagnose me- do surgery on one of the shoulders and now its so loose that the muscle is ripping. The pain is terrible and my current ortho is telling me to just keep doing physical therapy or look at a shoulder fusion.
@natronbetticus
@natronbetticus 7 месяцев назад
I'm 45. I've recently trained to be an RN in Canada, and have been practicing for about a year. I'd never heard of EDS before my girlfriend mentioned it last week. I'm almost certain I have it. Anyone know if chronic headache is a symptom?
@irishgirl81498
@irishgirl81498 7 месяцев назад
For sure - the ehlers danlos subreddit is a great place to search for specific symptoms.
@strangequarkproductions4942
@strangequarkproductions4942 Месяц назад
Yup. It's very common. ❤
@patientzero5685
@patientzero5685 Год назад
I had prolotherapy with dextrose. It did seem to help with ankles and wrists but not larger joints.
@melymel36
@melymel36 7 месяцев назад
Thank you for sharing, this gives me hope. I have an ankle injury that refuses to heal and I’d like to kook into trying prolotherapy.
@patientzero5685
@patientzero5685 7 месяцев назад
@@melymel36 I had surgery on both feet when I was a kid. I know how horrible recovery is! I still have terrible pain in both feet. If you can, get a CUSTOM orthotic to put in your shoe. The ones made of different density foam are the best. Using an ankle brace may help too. Try the prolotherapy if you can. I couldn’t afford to continue the treatments after lost my job. I hope it help 🥰. Never give up hope! Believe me, I feel your pain. You aren’t alone in this fight!
@melanievando2040
@melanievando2040 7 месяцев назад
I have EDS, POTs and chronic vertigo.
@johnspillman5403
@johnspillman5403 10 месяцев назад
There is limit to having the medical professional work on your body when they get things wrong 90 % of the time working on you thinking they no and understand the complexity of H/EDS and all other types, and bits you have from other types that you may have do fit into a neat little box the medical professional like to do,, 🙏 amituofu
@gafsabux8389
@gafsabux8389 2 года назад
Thank you for sharing ♥️ from Gafsa Bux 🇿🇦 ♿ 🦓 🌈
@MartinelunafayeWhitear21
@MartinelunafayeWhitear21 2 года назад
It's so hard to get diagnosed I'm starting to give up I cant jion in with my friends because pain I'll be in next day that can last for days drives me insane 😭
@bestoonisa9007
@bestoonisa9007 2 года назад
Hello. there is a cure . Florida doctor is already curing this without dangerous pills. see the testimony ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-x9gz1vtk8jU.html
@ILENEmusic
@ILENEmusic 2 года назад
Go to your PCP and ask for a referral to a rheumatologist or bone specialist
@melissastory1993
@melissastory1993 Год назад
I’ve been waiting for PCP/GP/Family Doctor for 7 months now after mine retired and there’s a shortage. Thankfully, I found a physiotherapist that has experience with EDS who understands how long and drawn out the diagnosis process can be. She’s been working with me to help me manage my pain and it has already helped sooo much. Although it’s validating just to be taken seriously, I can’t wait till I have an official diagnosis.
@redsheppard5618
@redsheppard5618 2 года назад
What about depression because of burnout (I think) because you have been pushing yourself so hard to be normal without knowing what was wrong. And always thought you are just weird and not capable.
@MrOoglebog
@MrOoglebog 2 года назад
That's me basically. I always was trying to keep up with others but simply couldn't without burning out and leading to injury. I was a little chubby as a kid so I thought that was the cause of my issues for some time. But then I got skinny and it never went away. Now I know better than to push myself, which has helped, but I still struggle with it.
@user-pe4jt9us7c
@user-pe4jt9us7c 8 месяцев назад
Anyone in Christchurch have advice re getting a diagnosis/know a GP with good awareness of EDS?
@beverlyquigley6608
@beverlyquigley6608 2 месяца назад
What if you have random tissue manifestations but only a hyper spine. Your youngest son has all hyper joints. And my middle had the appearance of marfan. I don’t know if I should see help.
@uyoebyik
@uyoebyik Год назад
I was able to stick my shoulder blades out at right angles
@louisebam1466
@louisebam1466 Год назад
I was on a benzodiazepine. I thought that was making me sick. Now I'm in trouble... Now my family don't believe me...
@catherinechandler3250
@catherinechandler3250 8 месяцев назад
Omg I think this is what I have. My mother has it too and both of my adult children. My son has dislocated his elbow twice and his shoulder once. My daughter has had digestion issues. I live with chronic pain. But the three of us can do great party tricks together. Where can we get help? We are in Wellington.
@xlReap64
@xlReap64 Год назад
To follow up on my comment, just by being skinny I always felt weak and frail, and the reality is I was and still am weak and frail, and those feelings are amplified by the fact I permanently have aches and pains, people just think I’m soft and exaggerating, I will kill myself soon
@trollsneedhugs
@trollsneedhugs 3 месяца назад
Get braces on all joints: ankle, knee, wrist, elbow, and ESPECIALLY neck. I feel much better already doing this!
@marsy1480
@marsy1480 7 месяцев назад
I was party trick girl reluctantly lol
@jeremysargefield9434
@jeremysargefield9434 9 месяцев назад
Hi I’m from Edmonton Alberta Canada i really need help there’s no drs here to help with EDS and there telling me only women can get EDS and I know it’s not true or is it I’m entersex I don’t know if that makes a difference please get back to me. I have no life I can no longer work every time I try. I pop my joints I get injured I can barely move. Takes me about four hours just to get out of bed. It’s to the point where I’m extremely depressed. I’m begging you help me.
@35neets
@35neets 6 месяцев назад
Yes men can have EDS too but there is a smaller proportion of them compared to women. I think mainly because men have more muscle to support joints than women. Don’t give up there is help out there but it takes some effort to find it unfortunately. Join the EDS community online. I’ve learnt many helpful tips from other sufferers to manage my pain.
@angelaquimby2360
@angelaquimby2360 Месяц назад
I have heds and all three of my sons have it also. So yes men can absolutely get it.
@meganmarts5769
@meganmarts5769 5 месяцев назад
I was diagnosed with eds as a kid in the early 90's. I finally got pregnant after several miscarriages and the pregnancy made my eds symptoms go out of control. Im unable to work. I applied for disability and i got denied. My doctor's are not listening to me. I need help
@Lionessliving
@Lionessliving 5 месяцев назад
Are you in uk? I went private to see Dr Paul Brennan in London. Diagnosed and now have a treatment plan. I pray that you get the validation and help you need.
@meganmarts5769
@meganmarts5769 5 месяцев назад
@@Lionessliving I'm in the US
@christoffeledmund2853
@christoffeledmund2853 2 месяца назад
🦓 Thank You 🦓
@cherylkiely2822
@cherylkiely2822 2 года назад
I have this. I’m getting worse for some reason?
@bestoonisa9007
@bestoonisa9007 2 года назад
you can get cured. see the testimony ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-x9gz1vtk8jU.html
@andrxmeda97
@andrxmeda97 2 года назад
EDS usually gets worse with age.. As a child i only suffered from like 3-4 symptoms, now at 24 it's like 20+ symptoms. I'm not living, i'm surviving.. I hope this disease gets more attention!
@gouachepottwo7537
@gouachepottwo7537 2 года назад
@@andrxmeda97 Yeah I had no idea I had it till it got worse. There is treatment but life is hard and you gotta keep fighting to keep above water. There is hope, try not to hate your body and take extra care and learn what helps. Goodluck 💚
@courtneyburgess1419
@courtneyburgess1419 Год назад
I had a major knee dislocation I had major ligament reconstruction again then post op injection major uhm drug reaction now Epi pen the back sprain and steroid injection then bulging c3 c4 neck then ankle sprain then I was dislocating my left elbow crutching post surgery then my right hip with my dysplasia my subluxing then I fell in my shower end up with a major concussion fluid in my brain unconscious post concussive for over a month I thought the pain would never end.. all from opening my fridge twisting and dislocating my knee cap snapping my patella ligament and everything got off balanced and spiraled But hey guess what? I’m ok now again. Ehlers people take a lot longer to heal, I was out of work for over six months and went through hell, I still haven’t gone back to the gym, but I’m not having massive pain attacks and I’m able to function. It does get better it does get worse because we just are special. I have a nickname, “gumby” I have good and bad months not days. But there is good Hope this helps Hang in there ❤
@courtneyburgess1419
@courtneyburgess1419 Год назад
Also not for nothing I am a critical care nurse and I’m back at it happily so 😊
@bearbait7405
@bearbait7405 11 месяцев назад
Ketamine RFA
@LaytonWin
@LaytonWin Год назад
It’s crazy how I only know one person who knows what this is.
@LaytonWin
@LaytonWin Год назад
It’s such a weird condition. I have two forms(classic and hyper mobile) and back in early to mid Highschool there was a lot of pain, but through lifting weights I have been able to keep pain to a minimum. The way I think of it, I build up my muscles to keep my joints in place, but still I have small weaker muscles that when get overworked cause injury (especially shoulders)
@Catlily5
@Catlily5 11 месяцев назад
Classical cancels out the hyper mobile type. Hyper mobile type is for people who have an unknown genetic cause.
@alexismarroquin9137
@alexismarroquin9137 Год назад
I don't want to know how you treat it find a dam cure
@christianigiovannini6741
@christianigiovannini6741 Год назад
All thanks to Dr Aba for curing me from EDS Am forever grateful
@blondbum
@blondbum Год назад
EDS isn't curable.
@courtneyburgess1419
@courtneyburgess1419 Год назад
@@blondbum yea it’s a chronic incurable disease..
@kuttiesrecipes9929
@kuttiesrecipes9929 2 года назад
I am from India I need treatment please help me
@tukitaki6936
@tukitaki6936 Год назад
There is no help in India
@trollmatroll8621
@trollmatroll8621 Год назад
@@tukitaki6936 srijani Bera?
@tukitaki6936
@tukitaki6936 Год назад
@@trollmatroll8621 not the same sorry
@geethaguthikonda9198
@geethaguthikonda9198 Год назад
Hi dear, please check orthopedic clinics in your city, these days some do provide the Prolotherapy treatment. Not sure which city you live in but, for sure there are treatment centers in Maharashtra, Tamil Nadu, Hyderabad. Please check it out.
@tukitaki6936
@tukitaki6936 Год назад
@@geethaguthikonda9198 hi maam, just asking do u believe in prolotherapy?
@bmac6645
@bmac6645 Месяц назад
Way too many interruptions by the reading panes.
@KC-gi9ol
@KC-gi9ol Год назад
The link in the description to Dr. Rabago’s assessment of this treatment protocol is broken. Here is the correct link. www.hqsc.govt.nz/assets/Consumer-hub/Partners-in-Care/Publications-resources/Prolotherapy-review-letter-Dr-Rabago.pdf
@HQSCNZ
@HQSCNZ Год назад
Thanks for letting us know. We've updated the link in the description.
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