Endometriosis Awareness Month March 2019

Posted on March 1, 2019March 1, 2019 by Andrew Orr

Dr Andrew Orr has an honest and open talk about Endometriosis Awareness Month and also about the disease itself.

Dr Andrew Orr talks about the facts, the myths and what women with endometriosis go through on a daily basis.

He also discussed that there is help out there and what is needed in a multi-modality (team like) approach to care and ongoing management of the disease

Lastly, he wants every women, and man, to know that Period Pain IS NOT Normal and that women do not need to suffer in silence. There is always help out there and you just have to find the right people who will care, listen and help you in every aspect that you need.

Dr Andrew Orr has a special interest in Endometriosis and does research and lecturers about this horrible disease that affects 1 in 10 women world wide. If you do need help with period pain, or endometriosis and the associated symptoms, please give his clinic a call. Please do not suffer in silence alone. There is help out there. Dr Andrew Orr’s motto is “No Stone Left Unturned” and he uses this to assist all his patients.

Take care

Regards

Dr Andrew Orr

-No Stone Left Unturned

-Women’s and Men’s Health Expert

01 Dr Andrew Orr 1

Living With Pain.

Posted on February 26, 2019February 26, 2019 by Andrew Orr

There are lots of people who suffer with pain daily and the one thing I do know for sure, as do many professionals I work with, is that many people who are in pain, or have inflammatory pain conditions, are not being managed really well.

There are so many aspects to pain and so many drivers that make it worse. Everything we do and are exposed to daily can drive, or exacerbate pain. Diet, lifestyle, alcohol, stress, drugs, medications, our environment, chemicals, additives, bad bacteria, disease states, moods and the way we think etc, can all drive and exacerbate pain.

In previous blogs and articles I have explained about how pain works, how long term medications can actually make it worse and also some of the alternatives to some of the hard-core pain medications.

Again in this video I talk about pain and want to let everyone know there is help out there to help you better manage pain.

Please know you do not have to do this alone and that there are professionals out there who can help you better manage your pain levels and get your quality of life back.

If you do need help and assistance in dealing with pain, please give my clinic a call and book in a consultation.

Take care

Regards

Dr Andrew Orr

-No Stone Left Unturned

-Women’s and Men’s Health Expert

01 Dr Andrew Orr 1

Sometimes The Body is Like a Well Sprung Spring & Other Times Not

Posted on February 21, 2019September 6, 2021 by Andrew Orr

Sometimes the body is like a well sprung spring, and over time the spring gets stretched, but , bounces back to its original shape, but overtime, one day, it will get to a point where it is slower to recoil to its original state, or, will no longer spring back to its original shape and have no more spring to recoil to its original state. No matter what you do to it, it just will not recoil and will in essence become to a state of non-repair.

As everyone knows, I always use a very integrative medicine/ multi-modality approach to treating people and getting the best for people’s health. I always believe that preventative medicine is the best approach to any health problems, but sometimes medical intervention, in the form of surgery, is needed for some acute complaints.

It is always hard when someone comes into the clinic and they are doubled over in acute pain from endometriosis, or an acute skeletal issue, and while I can help them, I know that the best thing for their long term health would be intervention in the form of surgery. That is not saying I cannot help and assist people with acute pain, but sometimes the best thing to do is get the person in for surgery to help with the acute pain, and then follow up with preventative and rehabilitation care.

Often it can take several months to help regulate hormonal issues and pain from conditions such as endometriosis, or pelvic inflammatory disease, with more conservative forms of treatments such as pharmaceutical medicines and hormones, complementary medicines, acupuncture, supplements etc. While the outcome after treatment is always great, is it really beneficial for people to endure constant pain for months, when surgery could produce a faster result, for the pain?

In saying that some of these conditions have a high rate of return, so that is where an integrative medicine/multi-modality approach can help post surgery.

I was talking to a medical specialist colleague recently, who promotes a holistic approach for all his patients, and he explains it to his patients like this;

“Sometimes the body is like a well sprung spring, and over time the spring gets stretched, but , bounces back to its original shape, but overtime, one day, it will get to a point where it is slower to recoil to its original state, or, will no longer spring back to its original shape and have no more spring to recoil to its original state. No matter what you do to it, it just will not recoil and will in essence become to a state of non-repair.”

I see people in my clinic just like this spring. Some are well oiled, and well sprung, and bounce back into shape very quickly. Some are showing the signs of starting to lose their spring, and then others have just pushed their body to the point or no spring, or worse still to the point of non-repair.

Obviously I like seeing people do the right things and use preventative health so that they stay well oiled and well sprung. I do like to see people coming into the clinic when they get the first signs of ill health and the spring is starting to recoil slowly.

The sooner you get onto any health complaint the easier it is to treat. Early intervention is the key to any disease state, or health issue. But, we all know people who push through pain and say “She’ll be right mate” and get to that point where they just can’t recoil anymore. Then we get the ones that have gone beyond that and unfortunately no matter what they do you will never be able to get them back to what they used to be like. So, please don’t ever let your body get to this point if you can.

The reason for this blog was to not only inform people to be proactive with their health but to also make sure people are covered if they do need surgery. It is always such a shame and I always feel sorry for people who need urgent medical attention, but they don’t have private health cover. I know that not everyone can afford it, and I am not pushing it either. But, it is worth considering for anyone who have a long term health issue, or especially for women trying to conceive.

Every woman is going to need to see a gynaecologist at some stage in their life and you don’t want to be relying on a failing public health system that could have you waiting months, or even years, for an appointment, or much needed surgical intervention. Those experiencing fertility issues will need some investigation at some stage so it’s almost necessary to be prepared and well covered.

I’ve seen so many people over the years that come into my clinic, for so many different ranges of acute conditions, that actually do require some sort of urgent surgical intervention, but only to find out they can’t get the necessary treatment they need because they aren’t covered.

The public health system is in such a mess at the moment and wait times are becoming increasingly long. If you have an acute condition, you don’t want to be waiting months, or years for treatment. The other issue is that you don’t get to see a surgeon of your choice and can then end up with the lucky dip of whomever is there on the day. The other issue is that this person may not specialise in the disease state, or issue you are there to have treated. This is what happens to many and this can then have long term health consequences if you aren’t given the right care that you need, or they actually miss crucial issues as well. It is a big issue.

Then when you finally get to having the surgical intervention, it may require multiple surgeries, and the first surgery may be just for investigation only. I’ll give you an example.

I had a friend, with acute period pain that got nausea, vomiting and even fainted, (from severe endometriosis) go on a 12 month wait list for surgery in the public system. Finally she got in for surgery only to wake up and find that the operation was one of many to come and the first one was only for investigation purposes only. She would need ‘three’ more surgeries spaced at months apart. So nothing was done with the first surgery, she was still in pain and now had to prepare for further surgeries.

Yet, a similar friend who had a private cover, got to chose the gynaecologist of her choice, got someone who specialised in her disease state, was an advanced trained excision surgeon, had no wait time, had not out of pocket expenses, had everything tidied up and the endometriosis removed on the first surgery. This same lady also saw me for assistance. There is a huge difference in the time, the surgeon who did this the surgery, the treatment and the amount of surgery needed.

As I said, it is a hard topic to talk about and is by no means a push for private health cover. I am only talking about this to educate people that sometimes it may be a necessary part of your overall health. It just distresses me seeing people who need desperate immediate help, not being able to get it. I know that not everyone can afford it and believe me you have to shop around when you do start looking at it. The big companies are usually the worst to deal with and the smaller companies are usually the best to deal with, and give you better rebates.

In saying that, private health is a sometimes necessary part of overall health care, especially for those with ongoing health concerns and especially those that may require some form of medical intervention. There are some great smaller funds out there that don’t cost that much and give you full hospital cover with an outlay of a couple of dollars per day. You can also look into having extra’s cover as well, which will cover part of the treatments with us also.

Again some of the smaller funds provide better rebates and the best thing would be to give us a call and we can tell you who those funds are. I hate talking about these sorts of things but at the end of the day I care when people aren’t getting the right help and am here to help people with every area of their overall health. It is a very important issue that we all need to consider and that we all need to discuss too.

If you do need help with pain, or a women’s health condition, help having a baby, or just need someone who cares and can help you get the right advice and health management, please give my clinic staff a call and find out how I may be able to assist you.

Take care

Regards

Andrew Orr

-No Stone Left Unturned

-Women’s and Men’s Health Advocate

-The Women’s Health Experts

-The International Fertility Experts

-The Endometriosis Experts

The Importance of Following Through With Advice, Treatments & Change

Posted on February 19, 2019September 9, 2019 by Andrew Orr

I see so many people who have been ‘missed’ and ‘dismissed’ and who have suffered in silence with their disease state.

But the biggest shame is when those that are offered real help, then do nothing with that advice and continue on the vicious, merry-go-round cycle of their disease.

My motto is “No Stone Left Unturned” and I apply that to every patient that I see. My initial consults are usually 1-2 hours in length and I also do lots of preliminary work prior to see a patient as well. I make sure all my patients are now only sent health appraisal questionnaires, but are also evaluated with mood and stress questionnaires for their mental health too.

I really want to delve into every fine detail of a persons life to see what may be driving their disease state and symptoms. It is to also help with diagnosing those that have not been properly diagnosed either. I then write up a comprehensive report for all my patients, with everything they need to do, the changes they need to make, the medicines they need to take, the investigations and testing they need to have and all their step by step health management moving forward. It really is a matter of ‘No Stone Is Left Unturned’ as I mentioned before.

As I mention in this video blog is that the greatest shame is those that come to get the advice and help and then do nothing with it. Just remember that if you do not change anything, or do the work needed, then nothing changes. The key to real change is actually within you.

If you so need help with a particular health issue, or you just aren’t getting the right answers and care, then please book in a time to see me and let me be your guide to better health and getting your life back to normal.

Let’s Talk About Fertility

Posted on February 19, 2019September 9, 2019 by Andrew Orr

Dr Andrew Orr has an honest and open chat about his years of experience dealing with couples with fertility issues.

Much of it gets back to couples not having the proper testing and investigations, being on the same page, preconception planning, getting healthy, doing the work and the expectations versus reality.

Have a listen to Andrew’s open and honest discussion about a very serious topic.

If you do need help and are struggling with fertility and not having a baby, Andrew can assist you in your journey to becoming parents.

To find out how Dr Andrew Orr’s fertility program, please call his friendly staff to find out more.

Endometriosis ‘Is Not’ An Autoimmune Disease

Posted on January 30, 2019September 9, 2019 by Andrew Orr

There are many statements made about endometriosis and many of them are not factual. This goes for the statement that Endometriosis is an autoimmune disease. In this article I will explain why this statement is false, and not true, and the reasoning behind it.

Everyday I get people telling me all sorts of facts and fictions they have heard on Dr Google. As I always say to people, Dr Google is not a reliable source of health information, unless it is from peer reviewed medical sites. Even then these sites are pretty much restricted to the general public.

Many people are looking for the miracle cure for endometriosis, or the holy grail of causes of it, and why wouldn’t you if this was affecting your life. I know from personal experience with health issues, I do want to know what the cause is and how to treat it.

But like so many conditions many people face each day, sometimes there is no answer just yet. Sometimes we don’t have all the answers and that is just how it is. When this is the case for a disease, I always tell my patients to not get caught up so much on the cause, but rather do the known treatments and management to get better. This is what really matters the most. Plus, like any disease, we need to look at treating the individual and not treat the masses.

Many diseases like endometriosis need a multi-modality approach to treat them effectively and this how I treat my patients and why I have so much success with treating endometriosis. It is about employing the right treatments and treatments that work.

Endometriosis does not fit the classification of an Autoimmune Disease.

What we do know is that endometriosis is made worse through diet and lifestyle and external influences. We also know that internally there are many things that exacerbate endometriosis too. Behind it all, it is an inflammatory based disease. Any inflammation in the body makes it worse. Plus, endometriosis itself can inflame the body too.

Endometriosis is very much an ‘autoimmune like’ disease, because inflammation is a major driving factor, but it isn’t an autoimmune disease. Endometriosis does not fit the classification of an autoimmune disease as it does not produce auto-antibodies. We also know that endometriosis is normal tissue growing in abnormal areas. Again not producing auto-antibodies.

What we do know

We know that retrograde menstruation is a big factor for some women, but we also know that retrograde menstruation isn’t a factor for others. What we do know is that estrogen is a big driving factor and that endometriosis is estrogen driven. It isn’t from estrogen dominance, or estrogen excess either. What we do know about endometriosis, is that like autoimmune diseases, it is also passed on via genetic and hereditary factors. But again, endometriosis is not an autoimmune disease and does not fit the classifications of an auto-immune disease at this stage.

Like many diseases we get in our body, we often have other disease states expressed at the same time and can be purely coincidental. Some can come from hereditary factors and people are just predisposed to getting this diseases and when the body is inflamed, it just causes this other diseases to be expressed too. If someone has an autoimmune disease and also has endometriosis, this does not mean that endometriosis is autoimmune. There are many women who have endometriosis and who do not have autoimmune diseases as well.

Inflammation is a driving factor

If a woman has an autoimmune disease at the same time as endometriosis, this is purely coincidental, or it is another hereditary factor that may have been passed onto them through their parent. It needs to be treated independently and not as part of endometriosis. It is all inflammation at the end of the day, so addressing inflammation and immune response will not only help the secondary autoimmune disease, but it will also help the endometriosis.

I’ve talked about the facts and fictions of endometriosis before and we really cannot say endometriosis is an autoimmune disease, because there is no credible, or conclusive research to back that up at this stage.There maybe in the future, but at this stage there is not, so we cannot say that endometriosis is an autoimmune disease.

Is the immune system & inflammation a part of endometriosis? … It sure is

Is endometriosis and autoimmune disease? … It isn’t at this stage

Hope this helps to shed some more light on this disease that affects so many women around this world. Hopefully one day soon we will have all the answers and we can end the horrible world of endometriosis.

If you want to find out more about how endometriosis is not an autoimmune disease, have a read of this great article by A/Prof Jason Abbott from Endometriosis Australia’s page. Click Here

Regards

Andrew Orr

-No Stone Left Unturned

-The Endometriosis Experts

-The Women’s Health Experts

-“Period Pain is Not Normal”

Endometriosis a burden on women’s lives

Posted on January 30, 2019September 9, 2019 by Andrew Orr

Research published in the Journal of Family Planning and Reproductive Health Care found that endometriosis affects women’s sex lives, personal relationships, work life, and emotional well-being.

Endometriosis often takes a long time to be diagnosed and affects all areas of a women’s life, a study has found. Endometriosis is a chronic, recurring disease that is experienced by approximately 10 per cent of women worldwide. This number could be greatly understated as many women have not being diagnosed properly and many women still think period pain is normal.

But, while period pain is part of endometriosis, a significant portion of women with endometriosis are asymptomatic (meaning no symptoms) and only get diagnosed when there is a need for fertility treatment.

Common symptoms include of Endometriosis
• Painful menstruation,
• Heavy menstrual bleeding,
• Painful sex
• IBS like symptoms
• Bladder issues (UTI like symptoms)
• Ovulation Pain
• Pain with bowel movement
• Chronic Fatigue
• Infertility

The Research Unit at the School of Public Health and Preventive Medicine, reviewed a number of papers that documented women’s experiences of endometriosis. The most common theme was that women had experienced delays in diagnosis.

Many women feel they are being dismissed and this is evident in the fact that it often takes up to “10 years, or more” for women to be diagnosed properly.

The study found that women were more likely to be diagnosed sooner when they approached their doctor describing symptoms as fertility-related rather than a menstrual issue.

The study showed that some women initially delayed seeking help for their symptoms because they believed all women had painful periods. When women revealed their symptoms to a family member, friend or medical professional their experiences were typically normalised as being what all women must endure. Period pain is not normal and all women need to know this.

The study also found that women often felt frustrated and angry at unsatisfactory experiences with healthcare providers, and had concerns about the effectiveness and side effects of treatments.

Women want their doctors to really listen to their experience and concerns. They want to explain the true impact of the condition on their lives, rather than simply rank their pain on a scale from one to 10, or be dismissed each time they try to have their doctor listen to what they are going through on a daily basis.

The study found that further research was needed to gain a comprehensive understanding of endometriosis as experienced by diverse groups of women.

This research will contribute to the improved health care of women with endometriosis in Australia, and around the world.

Too many women being ‘missed’ and ‘dismissed’

I see so many women who have been misdiagnosed, had symptoms missed and been dismissed for years and seen multiple healthcare practitioners, both medical and complementary.

There are clear-cut signs and symptoms that point to endometriosis and we need for healthcare practitioners to start to know this. We also need for practitioners and the public to know that endometriosis can only be diagnosed by a laparoscopy (surgical intervention) and that scans and blood tests, do not diagnose endometriosis.

Lastly, my message to all women is ….. “Period Pain IS NOT Normal” and people need to stop telling women it is.

There is too much BS out there about endometriosis and we need all women and all healthcare practitioners to start knowing the facts. 10 years, or more, to a diagnosis is unacceptable for any health condition. It means many women are being ‘missed’ and ‘dismissed’ along the way. Let’s put an end to Endometriosis.

If you do need help with period pain, or help managing endometriosis properly, then please call my friendly clinic staff and find out how I may be able to assist you.

Regards

Andrew Orr

-The Endometriosis Experts

-The Women’s Health Experts

-No Stone Left Unturned

Ultrasounds and blood tests have limited value for diagnosing some causes of period pain and menstrual irregularities

Posted on January 30, 2019December 4, 2019 by Andrew Orr

I know I have said this often, but it seems that every day I get another email saying that “I have period pain and I have been to the GP and done scans and bloods tests and he/she says that there is nothing wrong”

The problem is that there is something wrong and the first thing wrong is that someone was told that there is nothing wrong, when they have only had very basic testing done.

The second thing wrong is that most of these women are not being referred onto an appropriate specialist, which is what good sound ethical practice is. This is why some conditions like PCOS are taking up to 3 years to be properly diagnosed and conditions such as endometriosis are taking up to a decade to be properly diagnosed. It just should not happen.

I can’t begin to tell you how many women I have seen over my years in practice, that have been told that there is nothing wrong with them, or that the practitioner hasn’t found anything, when really all they have done is a basic scan and a few random blood tests. Then when these women are properly investigated we end up finding all manner of issues. Yet, these women were told that there is nothing wrong.

All I can keep telling people is that while ultrasounds can find some causes of gynaecological issues, there are many issues they cannot find. It also depends on the technician, or person scanning you too. I know that there are not that many specialised gynaecological radiologists and this is why many things do get missed. I have viewed scans that show abnormalities and the report says that everything is fine. This is why I will only ever read scans and not just reports.

Gynaecological issues such as endometriosis cannot be diagnosed by ultrasound and can only be diagnosed by surgical intervention, in the form of a laparoscopy and with histology. Then, as I have said many times too, it all depends on the surgeon you have seen. If your surgeon isn’t an advanced trained laparoscopic surgeon there is a very good chance you may not have been investigated properly. I have mentioned this in many of my previous posts.

Even some cysts, PCOS, polyps and other masses can be missed on scans and let’s not even talk about blood tests. Sure, some hormones levels can be a pointer to a certain issue, but they are not an accurate diagnostic. To be completely honest, many women with serious gynaecological issues will have normal hormonal levels and have completely normal blood results. This can even happen in certain cancers and why some of the cancer markers are now not being used as definitive diagnosis.

I can tell everyone that I have seen many gynaecological issues being missed, and women being dismissed over the years, and it still happens on a daily basis. If you have menstrual issues, or are in pain daily, or just with your menstrual cycle, and you are being told everything is fine, then you need to get a second opinion and a referral to a good specialist.

If you would like help with a women’s health condition, please give my friendly staff a call and find out how I may be able to assist you.

Regards

Andrew Orr

-No Stone Left Unturned

-Master of Women’s Health Medicine

-Women’s Health Expert

Why Iron Deficiency and Anaemia Should Be Take More Seriously

Posted on December 11, 2018September 8, 2019 by Andrew Orr

One of the common things I am seeing in women of all ages is iron deficiency and anaemia. Many women have very low levels of iron and are unaware of the dangers this may pose to their short term, and long term health.

We are also seeing women being hospitalised and seek emergency help due to iron deficiency and anaemia and this highlights that there is inadequate management and detection of a very preventable condition. It also means that many women are not taking this matter seriously enough and often put off seeking screening and then aren’t having their iron levels managed properly.

I need to let all women know that having low iron can be very dangerous. It is something that should not be glossed over, or taken lightly. Iron deficiency can and does cause short term and long term health complications.

Iron deficiency can raise the risk of the following health conditions

Coronary heart disease
Stroke
Osteoporosis
Compromised immune system
Increased risk of infections
Tachycardia
Heart failure
Enlarged heart
Lung problems
Muscle aches and cramps
Restless leg syndrome
Delayed growth and development (mainly in children)

These are just some of the health issues that being low in iron can cause and it very important that we start educating all women and healthcare providers about the importance of iron.

What are the symptoms of Iron Deficiency and Anaemia?

Fatigue
Weakness
Dizziness
Fainting, or feeling of feeling faint
Pale skin
Breathless
Frequent headaches
Palpitations or racing heart
Easily irritated
Difficulty in concentrating
Cracked, or reddened tongue, sore tongue
Loss of appetite
Strange food cravings such as wanting to eat dirt, or clay
Cold hands and feet
Brittle nails
Hair loss
Tingling, or crawling feeling in the legs

Iron deficiency is a very common cause of fatigue and other health issues in women and men, but is more commonly seen in women. Iron deficiency is also the most common cause of anaemia.

What are the causes of Iron Deficiency and Anaemia?

Heavy menstrual bleeds
Endometriosis
Adenomyosis
Fibroids
Polyps
Coeliac disease
Inflammatory Bowel Disease
Stomach or intestinal ulcers
Pregnant and Breast Feeding Women
Certain Cancers
Vegetarians and Vegans
Eating disorders and food restriction
Girls going through puberty
Certain illnesses

Heavy menstrual bleeds and gynaecological condition’s such as Endometriosis, Adenomyosis, Fibroids and Polyps are some of the main causes of iron deficiency and anaemia in women. This is closely followed by dietary inadequacies and food and nutritional restriction.

Many women have undiagnosed gynaecological conditions which are the cause of their iron deficiency and anaemia. Some of these gynaecological conditions will require surgical interventions to be diagnosed properly.

How are Iron Deficiency and Anaemia Diagnosed?

Your healthcare provider can organise routine blood tests to test for iron deficiency and anaemia. These will include the following

Full Blood Count (FBC)
Iron Studies

These tests will provide the following information on :

The Total Iron level in your blood
Ferritin levels
Total iron-binding capacity (TIBC)
Iron saturations levels
The red blood cells size and colour (RBCs)
The white bloods cells (WBCs)
Haemoglobin
Hematocrit ( the percentage of blood volume that is made up of RBCs
Blood platelets

Other tests

There are other tests to check for the cause of iron deficiency and anaemia and these could include stool analysis (check for blood in stool), endoscopy and colonoscopy ( surgical intervention gastrointestinal bleeding) and laparoscopy (key hole surgery for gynaecological conditions)

Treatments for Iron Deficiency and Anaemia

Diet– A healthy diet that is rich in proteins, vegetable and iron rich foods is the best way to ensure your iron levels stay at optimum levels. A proper diet should include leans meats, seafood, nuts, seeds, healthy oils, green leafy vegetables and other coloured vegetables, and moderate fruit intake.

Supplements– Supplements will help to keep iron levels and vitamin B12 levels in optimum ranges. Iron supplements are very much needed if you are vegetarian, or vegan. There is now research to show that women who experience fatigue will benefit from supplemental iron, even if their iron levels and ferritin are within normal range. Those with heavy menstrual cycles, or those whom have inflammatory bowel issue should also be supplementing

NB- All iron supplements should be taken with vitamin C to help with absorption. Many iron supplements also cause constipation and therefore you should get a good one that does not interfere with your bowel habits and is more easily absorbed. Many of the mineral based iron products are not absorbed well and do cause gastrointestinal upset.

I always recommend a specific practitioner only brand to my patients because it is better absorbed, and it does not interfere with the bowel habits.

Iron Infusion– Sometimes when iron gets too low, supplements just will not be enough to get iron levels up to where they should be quick enough. This is where iron infusions can be very effective. Please see my post on when you need to use and iron infusion. (Click here)

Treating the underlying cause of bleeding

Supplements will not help if the cause of the iron deficiency and anaemia is from excessive bleeding. It may help a little, but it will not be enough. Even iron infusions will only be short lasting if you don’t treat the underlying cause of the bleeding issue. Extreme cases may even need a transfusion to get iron levels and blood levels back up to optimum. This is why it is important to screen for underlying gynaecological conditions that can cause heavy and excessive bleeding.

If you are getting low in iron if means there is something wrong and there is a deficiency that needs to be addressed. Please do not take iron deficiency lightly and always be prompt to find the causes and restore optimum levels of iron in the body.

Prevention is a must

Prevention is always the best way to treat any health condition and this goes for iron deficiency as well. Ensuring you eat a healthy diet with iron rich diet is a great start. As said before, vegetarians and vegans are going to have to supplement and work really hard with their diet to ensure they get adequate iron. Even then it can still be hard as plant based foods just do not have the iron levels that meats, eggs and seafood’s have.

Make sure you also have lots of vitamin C in your diet to help with iron absorption and it is a good idea to supplement with vitamin C to ensure you get the right daily intake.

Final Word

If you do think you might be low in iron or have anaemia, please make sure you talk to your doctor, or your healthcare practitioner. Please do not supplement with iron without checking your levels first. Having too much iron can be dangerous and you also need to make sure you do not have hereditary high iron (haemochromatosis), which can present with the same symptoms as low iron.

If you are found to be low in iron, then please make sure you take prompt action to restore your iron levels and also make sure you are screened as to why you are low in iron in the first place.

Iron deficiency and Anaemia can be very serious and should never be taken lightly. Please always consult with your doctor, specialist, or healthcare practitioner for the most effective ways to keep your iron levels in healthy ranges.

Take care

Regards

Andrew Orr

-No Stone Left Unturned

-Women’s and Men’s Health Advocate

-The Women’s Health Experts

Insights into Endometriosis

Posted on November 29, 2018September 8, 2019 by Andrew Orr

Previously I posted a story about endometriosis being aired on SBS television. I am sure many people watched it and it is great to see that sufferers are finally being recognised. It is important that sufferers are finally being recognised and that there is more education about this disease.

But, is education and awareness enough?

Well, ‘yes’ and ‘no’. I always say this when I am asked this question. Yes, it is great to get education and awareness out there, but what are we doing to support those who are struggling daily?

Any education and awareness about this horrible disease is great. It is a huge win for sufferers when we do see programs go to air and aren’t scared to ask people their experiences of living with a disease state.

I do think those that were involved and those that are driving this awareness need to be applauded. Getting media to listen is one of the best ways to bring awareness to the disease states such as endometriosis.

While there was lots of information shared, I do believe more could have been talked about. I was a little disappointed to hear that the opening line was more about associating endometriosis and periods. We know endometriosis and its symptoms can be there daily, not just around the menses. But, it does open up discussion for more programs and media recognition for those with endometriosis, or any gynaecological condition really.

I’ll talk about the good things, the not so good things and everything in between. Let’ have a look what was talked about and some of the things that should have been talked about as well. I do realise time constraint mean that not everything can be talked about either.

The important things that were talked about

Millions of women world-wide suffer this disease
Millions of suffers do have a wide range of symptoms that vary with each individual
Period Pain IS NOT Normal
There is no cure for endometriosis
Millions of women world-wide have been led to believe their symptoms are normal, when they aren’t
Women are being missed and dismissed daily and told to basically suck it up
Many women take more than 10 years to be diagnosed
GP’s and other healthcare people are missing the disease and also failing to refer on
Many women are misdiagnosed for other disease states such as IBS, gastro etc
When presenting for medical help, many women are told they just have a gastro virus, or it may be an ectopic pregnancy
Endometriosis affects the daily life of sufferers and their partners and family as well
Partners can be affected by watching their loved one go through this disease state
Intimacy and a happy healthy sex life can be hard for sufferers due to pain and associated symptoms
Many endometriosis sufferers have to take pain killers daily, just to get through their day
Endometriosis requires a laparoscopy to be diagnosed
Scans and blood tests cannot diagnose endometriosis
Women need a highly specialised surgeon when needing to have the disease diagnosed and cut out
Despite the best medical treatments available, women are still in pain daily
Many women will require multiple surgeries to deal with endometriosis
Despite multiple surgeries, women are still in pain and have all the associated symptoms of endometriosis.
Women will need hormones, pain medications, pain management and psychiatric help dealing to be able to deal with endometriosis
Often pain and associated symptoms are not managed well at all
Women who suffer endometriosis are holding down jobs and many people are unaware they are suffering this disease
Many women with endometriosis cannot hold down fulltime employment either
Women are not being told the facts about endometriosis
Many healthcare practitioner do not know the facts about endometriosis
Women of all shapes, sizes and colour have endometriosis
Endometriosis is just as common as many other well-known disease states, yet little is known about it.
Complementary medicines such as acupuncture and Chinese medicine may help women with endometriosis (although this was brushed over very quickly)
Genetics/hereditary links are now known to be a big part in the disease expression

Important things that were not talked about

Endometriosis pain and associated symptoms do not just happen around the menses
A significant portion of women with endometriosis are asymptomatic (meaning no symptoms) and are only diagnosed through needing to assess for other issues such as fertility investigations
Not all women with endometriosis will experience fertility issues
Pregnancy does not cure endometriosis
Hysterectomy does not cure endometriosis
Endometriosis is Estrogen driven and not caused by estrogen dominance
Progesterone in suppressive to the disease
Pain levels are not related to the extent of the disease
Teenagers are not too young to have endometriosis
Certain combined contraceptive Pills that contain estrogen, could be making the disease worse, or in fact helping mask and then drive the disease
The facts around endometriosis need to be standardised and more freely available
Despite the best medical treatment not working for some women, we need to educate about other alternatives, including complementary therapies
Women with endometriosis do need a multimodality (team) approach to manage their disease state and daily symptoms
There needs to be better funding to help women access all services they need for endometriosis and the associated symptoms
Too much surgery can be just as bad as not having surgery
The first surgery should always be a sufferer’s best surgery
Women with endometriosis need to see and advanced trained laparoscopic surgeon who specialises in endometriosis and is an excision specialist.
Not all gynaecologists are advanced trained and not all gynaecologist will be able to effectively manage endometriosis
Most of the good advanced trained surgeons do not do public work. Some do limited work, most don’t.
Women and healthcare practitioners need to be educated about the facts are endometriosis
GP’s and other healthcare providers who are the first point of call for women, should be better educated about endometriosis and the associated symptoms
Women with endometriosis can have adenomyosis, PCOS and other gynaecological diseases at the same time
Women who suffer bad symptoms of endometriosis have contemplated suicide, or had suicidal thoughts
Women with endometriosis will require help with depression, anxiety and other mood disorders
Many women with endometriosis are addicted to pain medications and opiates and are not monitored , or managed well
Many women cannot function without some of the pain medications and the alternatives that are not as addictive need to be discussed
Diet and lifestyle changes can help with reducing the symptoms of endometriosis and may help with reducing some of the inflammation driving the disease
Healthy gut bacteria and restoring the microbiome can help with some of the symptoms associated with endometriosis and the inflammatory processes around endometriosis
Exercise may assist with the symptoms of endometriosis

There are probably many other things that need to be discussed, but, for now this is a great start. Any awareness is a great outcome and again those that were involved need to be applauded and commended. The sufferers, the specialists, the partners, the families, the media people and everyone involved deserve to be praised for this story. We now just need to take it to the next level of education and awareness for the sake of those and their families that suffer from this horrible disease.

There is no cure for endometriosis and even with surgery and the best medical interventions; women will still suffer the daily consequences of the disease. The best way to treat and clinically manage endometriosis is with a multimodality (team) approach that requires many different modalities and medicines. While there is no cure, with the right interventions and management women can become asymptomatic (meaning no symptoms). We now just need governments to provide better funding to this with endometriosis and those who will ultimately be involved in their care.

Let’s hope that with awareness and education, this brings further funding and changes. We also need for more programs to be aired on the media to talk about what women with endometriosis can do to manage their disease better and where to access the help they so desperately need.

Take care

Regards

Andrew Orr

– No Stone Left Unturned

– The Endometriosis Experts

– Women’s and Men’s Health Advocate