Your Hormones and Hashimotos


Many women with endometriosis or other chronic conditions, tend to suffer from more than one ailment. I invited a friend who is currently battling Hashimotos to talk about the hormonal connection between conditions.


Hashimoto’s, Endometriosis and PCOS have plenty of things in common: they all target women, they’re all chronic, and they all wreak havoc on hormones. It’s no wonder they are often seen together! Despite being separate diagnoses, the comorbidity between these conditions is incredibly high. A study published in the European Journal of Endocrinology reported 3-4 out of every 10 women with PCOS also have impaired thyroid function due to Hashimoto’s Disease. Comorbidity rates for Endometriosis and Hashimoto’s are reported as anywhere between 20-41%. These figures are not at all surprising to anyone who is a part of the online community of women with chronic illnesses, where it is easy to see a trend towards multiple diagnoses. 

Our hormones control so much, and if they aren’t happy, you will definitely know about it. Before I was first diagnosed with Hashimoto’s, I was going through such a hormonal nightmare that I was convinced I was pregnant. A thyroid condition never entered my mind. Instead, faced with rapid weight gain, exhaustion, hair loss, brain fog, painful and swollen breasts, intense cramps, and spotting, I decided that the only logical explanation was pregnancy. At this time I was on the pill, so pregnancy didn’t exactly make sense, but nevertheless I took 4 different pregnancy tests, alone in a supermarket restroom in a foreign country. Of course, they all came back negative. I didn’t believe them. What else on earth could be having such a dramatic and devastating impact on every part of my body, mind and health? I went to the doctor to ask for a blood test, explaining my symptoms and my belief I must be pregnant. The tests came back with a diagnosis for Hashimoto’s. 

The irony is, one of the first things the doctor said to me was “You will never conceive a child, or carry a child to full term with your thyroid numbers like this”. There I was, having been stressing over the possibility that I might already be pregnant, being told that it was in fact, impossible in my current state. 

Before diagnosis I had a vague understanding of the symptoms of Hashimoto’s, but I was oblivious to the fact that it was linked to infertility. Infertility is an issue that sufferers of Hashimoto’s, Endometriosis and PCOS are all forced to think about, whether they are ready to or not. In doing so myself, I came to a better understanding of the drastic impact of hormones in the female body. It is my belief that the hormonal component of Hashimoto’s, Endometriosis and PCOS is what links them so frequently in cases of multiple diagnoses. 

The silver lining for those suffering with Hashimoto’s is that while conception may be more difficult than average, if your thyroid levels (free T4, free T3 and TSH) and in good ranges and have been kept steady with the appropriate dose of medication, healthy pregnancy is definitely possible. It is much more difficult to get these levels in check and managed the sooner you are aware of them, which is why I am passionate about encouraging women, and in particular women who suffer from Endometriosis or PCOS who already are dealing with temperamental and every changing hormones, to have their thyroid tested. 

If you suffer from Endometriosis or PCOS I would urge you to have your thyroid checked more regularly than what is typical for those without these conditions. A yearly blood test is a good way of keeping an eye on things, but don’t hesitate to ask for one at any point during the year if you feel like you are experiencing symptoms. Make sure to ask your doctor for both free T4 and free T3 as well as the standard TSH, as these will be much more revealing. Given that you already have a diagnoses, I would also recommend asking for a TPO antibody check, which will confirm a Hashimoto’s diagnosis. 

If you have any questions about my experience please get in touch via the contact page on my blog or via my instagram page @the_thyroid_diaries.

Georgia. x


Janssen, OE et al, High prevalence of autoimmune thyroiditis in patients with polycystic ovary syndrome, Eur J Endocrinol. 2004 Mar;150(3):363-9


Georgia also discusses how acceptance can help prognosis in her latest blog post so definitely check that our too. I found her words resonated deeply with me, as it wasn’t until I accepted my limitations that I felt free.


Physiotherapy with Natalia

For me, physiotherapy is so much more than just working on my pelvic floor. This is because so many other parts of the body get pulled into the endo pain process. When you’re in pain you tense your pelvic and abdominal muscles, this leads to tension in your hips, and walking in a ‘protective’ manner. Now your legs and lower back begin to ache. A combination of stretching and strengthening, rolling on a foam roller, manual release of the pelvic floor, and massage into all those areas has helped play a role in getting me back on my feet for more hours of the day. I hope to continue to share techniques with you, so you can try and achieve some of these things at home.

Today I asked my lovely physiotherapist Natalia, to share with you how to stretch out your hips and prevent pain often associated with endometriosis and other gynecological conditions. Natalia has been treating me for a few months now and I can already feel the difference. I have less pain in my hips, lower back and legs, the ability to walk for longer periods and a feeling of overall greater strength in my body. Here is what she had to say…

“When dealing with endometriosis and pelvic pain it is sometimes difficult to get moving and to know where to start when it comes to exercising and stretching.  Stretching the hip muscles can really help to loosen up the pelvic floor muscles as well because of how closely these muscles interconnect.  Try some of these simple stretches to improve hip movement, increase blood flow, and stretch the pelvic floor muscles.

The Frog stretch: Get onto hands and knees with your knees out wider than your hips, you can stay on your hands or you can move to your forearms to get a deeper stretch.  I like making this stretch more dynamic, so rock forward onto your forearms and then backward sinking into your hips.  You can also turn your head side to side and imagine bringing your nose toward your knee and alternate side to side.  You will feel a stretch in your inner thigh, buttocks and in your hips.

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The hip flexor stretch: Place one foot onto a stool or chair, and with both feet facing forward lunge forward stretching the hip on the back leg. You can place your hands on your hips or bring them overhead to get more of a stretch in the abdominals and a deep stretch in the front part of the hip.  Once again, I like to make this dynamic to increase mobility and improve blood flow, so I move in and out of this stretch as well.”

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For more information on how to get in touch with Natalia, her details are below 🙂

Natalia Farnsworth PT, DPT, CAFS

Doctor of Physical Therapy

Certified in Applied Functional Sciences

SPEAR Physical Therapy

30 Broad Street- Ground Level A

New York, New York 10004

t: 646-790-7454  f: 212-379-2076


Pelvic PT – The missing link in your endo treatment plan

Getting my diagnosis for adenomyosis was one of the most psychologically traumatic experiences. On the one hand, I was so relieved when the doctor said he could see this additional disease on my scans and during the lap, because it explained why I was still in so much pain after TWO excision surgeries for endometriosis. On the other hand, the treatment options according to my surgeon were hormones (which I react badly to) or hysterectomy. I was devastated. I wanted a family above all else. But I was in so much pain every day. This was the beginning of a health journey to find other ways to cope with the constant uterine cramping and contractions. I sought a second opinion from a renowned gynaecologist and was referred to a pelvic physiotherapist.Not only did she help to reduced the tension and spasms occurring in the surrounding pelvic muscles, but it provided a much needed outlet for my struggle with this disease on a weekly basis.

Today I interviewed the lovely Dr Susie Gronski to provide you with all the info about pelvic PT and hopefully help you on your journey to a pain-free life.

Dr Susie

Me: How did you get into pelvic PT?

Susie: Funny that you ask! I think pelvic floor PT found me <chuckle>. After graduating from PT school, I couldn’t sit still. I’ve always been interested in neurology and focused my career on working with patients who’ve experienced a stroke, traumatic brain injury, spinal cord injuries, balance disorders, and vertigo (fancy term for dizziness). To tell you the truth, I was bored. I kept wringing the juice out of each job and looking for bigger challenges. Then one day a friend of mine told me about an opportunity to observe a pelvic floor therapist in my area as she was looking to hire on another therapist and was willing to provide training. At the time, pelvic floor PT never crossed my mind! My gut was telling me to pursue this curiosity of mine, so I did. I’m so glad I did! I discovered my heart’s passion for pelvic floor therapy and visceral manipulation, both of which have changed my life, professionally and personally. Since discovering my niche for such a specialty, I’ve transitioned into private practice where I have the freedom to provide care without limitations. Quality care that I believe everyone’s entitled to.

Me: What are some of the common issues you see and treat?

Susie: This one is tough to answer mainly because I see a variety of conditions in my clinic. I treat both men and women and generally the most common issues are pelvic pain. I also see patients with the following:

  • bladder issues, such as: urinary urgency-frequency (having the urge to urinate frequently), stress urinary incontinence (loss of urine with activity), or a combination of both
  • bowel issues – constipation, IBS, bloating, slowed intestinal motility, hemorrhoids
  • tailbone pain while sitting
  • pain with intercourse and/or pelvic exams
  • difficulty with orgasm
  • erectile dysfunction
  • prostatitis; also known as chronic pelvic pain in men
  • pregnancy related pain and post-partum care
  • adhesions – from abdominal/pelvic surgery or inflammation
  • pelvic pain associated with endometriosis
  • post-prostatectomy related erectile dysfunction and urinary issues
  • penis pain
  • nerve entrapment syndromes

The list could go on and on! One of the many reasons why I love pelvic floor PT is for the variety of conditions seen and the challenge of creating a treatment plan specific for each patient’s individualized needs and goals.

Me: How can pelvic PT benefit women with endometriosis or chronic pelvic pain?

Susie: In one study I’ve read, approximately 30-50% of women with chronic pelvic pain have endometriosis. Some go undiagnosed and many have the disease but are asymptomatic. A common issue that I see with women who have endometriosis is deep pelvic pain with intercourse, disrupting their overall quality of life and satisfaction. Typically, those with pelvic pain have over active pelvic floor muscles that are guarded and shortened. Pelvic floor PT can help by releasing tight pelvic floor muscles, manually working to release tender points and connective tissue restrictions found during the exam.

Aside from just working inside the pelvis, it’s also beneficial to look at the supporting pelvic structures, such as: hips, abdomen, and spine in order to rule out any other contributing factors to sub-optimal pelvic floor function. I always say that the pelvic floor is like a trampoline. It needs to be elastic to function properly. I also think visceral manipulation has excellent outcomes when it comes to pelvic pain and adhesions (fibrous bands that form between tissues and organs) that result from the endometrial tissue itself or from surgery. Pain in the pelvis can be referred from organs, and in cases such as endometriosis, it’s important to assess the mobility of the bladder, uterus, and rectum. Endometrial tissue can proliferate in between these organs and within the pelvic wall itself, therefore mobilizing pelvic organs can definitely help create balance within the pelvis by improving fluid dynamics, decreasing pelvic congestion, and abnormal tissue tension that might be compromising sensitive nerves through the pelvis. A healthy organ is a mobile organ. Motion is lotion!

Other helpful treatments include regulating the nervous system down with deep, diaphragmatic (belly) breathing, guided relaxation of pelvic floor muscles, pelvic stretches, functional movement integration, etc. Every patient that walks through the door is unique and should be treated as such. There isn’t a cookie-cutter treatment protocol for those with pelvic pain. You kind of just have to do what works best for that patient.

Aside from all the hands-on work therapists can provide, I feel that the support and coaching that therapists provide is priceless. I’ve been blessed to be able to provide a safe space for my patients to tell their story. To be heard. To be listened to. The greatest gift is often times silence. It’s unfortunate that I still hear things like, “I tried to tell the doctor but they just didn’t listen to me.” I’m a firm believer in trusting our body’s own inner wisdom to heal. As a pelvic floor PT, I feel that it’s very important to not only educate patients about pelvic floor anatomy and function but to also support and empower them to be their own healthcare provider; trusting in their own intuition to make the best healthcare decisions available to them.

Me: Are there any strategies women can use if they are at home and in pain?

Susie: Great question! I encourage everyone to practice B.L.I.S.S.I.P.L.I.N.E

Here’s what it means:

Breathe- do practice deep belly breathing throughout the day

Laugh- laughter is therapeutic. You can only experience one emotion at a time, so laugh often!

Invest- investing in your health is the greatest gift you can ever give yourself

Silence- take 5 min out of your day to be in the moment, meditate often

Stretch- gentle stretching helps increase circulation, improves mental health and flexibility. Also helps relax pelvic floor tension.

Intuition- trust in your own body’s inner wisdom to heal. Follow your gut when making decisions about your health. Remember, you’re your own best healthcare provider.

Positiveness- your perspective is everything! If you think it, it must be true.

Let go- relax and treat yourself. Even if it’s wearing a sexy pair of underwear! A great quote: “pain is an ideal habitat for worry to flourish”- Eccleston

Ink- there’s something about writing it down on paper. Keeping a journal helps cope with anxiety and stress improving your overall mental health and wellness.

Nourish- eat real food and hydrate, hydrate, hydrate! Eliminate sugars, processed foods, and artificial preservatives. Start incorporating foods that are more anti-inflammatory.

Exercise- add in a little bit of light activity to your day. This could range anywhere from talking a short walk to just putting the dishes away. Make “exercise” fun and modify it to your lifestyle. Remember, “motion is lotion and rest is rust”- Mike Stewart

Me: Do you have any thoughts you would like to share with women suffering from pelvic pain?

Susie: No one ever said the journey would be easy but they also didn’t say that you can’t love yourself along the way.


Dr. Susie Gronski, DPT, PRPC is a Doctor of Physical Therapy and a Certified Pelvic Rehabilitation Practitioner. She has a private practice in Willow Springs, IL where she treats men, women, and children with pelvic health conditions. She loves blogging and staying connected with her followers. Her mission is to spread the word about taboo health subjects with a little twist of humor. If you’d like more health tips from the pelvic expert please join her community and connect with her on:


Instagram-logo-005 @dr.susieg


p.s. check out Susie’s website for my interview with her on living with endometriosis.

Empowering women to fight for the best treatment

Increasingly, the internet community is becoming a fantastic research for women suffering and seeking answers as the medical community is slackening it it’s duty to care. There are groups run be registered nurses and patients who have scoured medical journals in order to be armed with the best advice to help women receiving inadequate care.

Unfortunately, I have recently noticed a very strange phenomenon on the endometriosis Facebook groups. Women are coming to these groups confused about the conflicting medical advice, failed treatments and guilt for their continued poor health. They come to these groups seeking direction on where to go next. The advice from the admins and old timers on the groups is often solid, medically correct and factual. However, it is delivered in a callous and abrupt manner, without explanation of the situation or worse, with blatant disregard for the individuals personal journey or choices. If this were a medical professional they would be labelled as having a poor bedside manner. The patient would be left feeling uncared for and confused about how to proceed. They would be unsure of whether to intrust such large decisions in the hands of someone that doesn’t seem to genuinely care about their personal situation, but rather treats them as a statistic.

I understand the people running the groups have the very best intentions. They donate their time to a cause that desperately needs more intelligent and driven people. They are fighting for better care and treatment for millions of women suffering worldwide, AND they are time poor (as are the few surgeons performing expert excision surgery.) But we know bedside manner is important, not just in making the patient feel comfortable but also guiding them in making the best decision for their health. Because what is the point of education if the advice does not lead to real change?

Too many women on these groups are afraid to seek help and ask questions. That is not the environment of empowerment that we should be striving to foster.


Coachella for the chronically awesome

I wanted to share my Coachella experience with the spoonie community. I was so excited to see so many fantastic artists, but it turned out to be a lot of hard work. Luckily, there are a few simple ways to make it an enjoyable experience for someone with a chronic illness.


Day 1

Was a total disaster. We had no idea where we were going. Our uber driver was a lunatic, swearing at the traffic monitors, so we ended up getting dropped off about 2 miles out from the festival. It was a long old journey to get to the stages, without about 3 check points involving waiting for 20 minutes in each line. Our wrist bands didn’t work, so we had to treck across from one end of the festival to the other in order to get them activated. This is no mean feat, Coachella is almost 30 square miles! By the time we got to the stages I was exhausted. My back and abdominal area were aching. I lasted about 15 minutes before I called quits and made the journey back out to the uber station.


Day 2

I spent some time researching Americans with Disabilities Act (ADA) and their provisions at Coachella, turns out there is a golf buggy that can come and pick you up!  However, I didn’t plan far enough in advanced, when I got there it was a 30 min wait until the buggy could come and get us. My partner and his friends were going to miss one of their favourite musicians, I felt too bad to make them wait, so trecked again from the uber drop off (at least not as far as the day before.) I managed to stay a little longer than Day 1, and i got to see Disclosure! Sam Smith came out and I would be lying if i said I didn’t have a little dance to Omen and Latch 🙂 but the standing and walking around again left me very sore and ready to put my feet up.


Day 3

We finally figured our shit out! I called the ADA unit in advance, there was a golf buggy waiting for us on arrival. At first the guy looked at me and didn’t believe I was there for ADA because he has so many people hassling him for a ride all day. When he realised I was legit, he felt terrible and apologised profusely, saying they don’t discriminate #invisibleillness. We skipped all the queues and got dropped right inside the festival! I couldn’t have been happier to arrive there without already being in pain. He also took as to the ADA tent, where I got a wrist band allowing me to skip the lines and give me access onto the viewing platforms (if you want to do this make sure you arrive 20 minutes before the show starts to get a seat.) I had an incredible day 🙂

What I learnt is that most big organizations will go out of their way to help people with a disability, and Coachella certainly does not let down the spoonie community! You just need to do some research and be prepared.

For more information on how to make next year and enjoyable experience visit their site.


Feel free to contact me if you have any questions about my experience at Coachella.


Nat xx


Cookie Monster

If you are like me, then cooking is hard work. I mean climbing a mountain hard. By the time I have finished cooking a meal my pelvic area and lower back ache so much that I no longer even feel like eating.

Although I originally liked to make everything from scratch, I am finding that it is actually better for me to take short cuts so I can reap the benefits of my effort. One example of a short cut I have found to be very helpful is using a quality gluten and dairy free cookie mix (I have a major sweet tooth.) The work involves tossing the mix in with an egg and butter alternative of your choice and plonking tablespoon size pieces of dough on a baking tray before cooking for 15 minutes. And they are soooo delicious…


There is an easy trick to assessing the quality of a pre-packaged mix – pick which ever brand has the shortest ingredient list. Another tip is to look for natural sweeteners such as raw or coconut sugar. If I am baking anything from scratch I will generally use fruit to sweeten, such as a banana, or molasses which is full of minerals.


Below is the brand I used for this batch. I found it at Wholefoods (San Fransisco) but you can also buy it online. All these pics have got my tummy rumbling again, I am off to eat half a dozen cookies 🙂 xx Nat

IMG_20160420_195152 (1)

Fighting For Our Life

Endometriosis isn’t just excruciating pain each month, mind numbing fatigue and frequent nausea that inhibits my ability to enjoy any food, it is also an extreme emotional rollercoaster and something has stopped me enjoying life in a way that most people would take for granted.

Not only do I have monthly labour-like pain, but since I did not receive early treatment for horrendous period pain and excessive bleeding (despite hundreds of tests and medical appointments), the condition became chronic. Now I suffer every single day. My day goes like this… I get woken up by a deep pulling pain just under my belly button, I stumble to the bathroom but that just makes the pain worse. So I scramble to get some painkillers. Within 45 minutes I finally feel a slight reduction in pain, enough to allow me to prepare something to eat (something plain of course, because otherwise I’ll spend the rest of the morning trying to subside my nausea). At this point, I will either still feel pretty terrible and resign to the fact it will probably be a non-eventful day, or pull my broken self together and try to do an activity – get the groceries, clean the bathroom, go for a walk. By the time I get home, I have an ache in my back so intense that I have to lie down. It doesn’t really go away until I have been horizontal for an hour and taken some strong painkillers again. Then I will try to get up again – I am stubborn like that. I will keep trying to get up, because the alternative is that my life is pretty pointless. I might try and prepare dinner or meet a friend for coffee. Either of those activities will trigger my lower back pain again. Otherwise, I’ll just cancel plans entirely, unable to get off the couch because I am too exhausted to even lift my own arm and change the TV station. As a result of this daily struggle I can not pursue a career, I can not have a social life, I can not play sport, I can not be an active and contributing member of my family or my society. And I am not alone. Although my case is extreme, there are 176 million women worldwide that endure what I described above to some extent. Firstly, no one should have to go through that suffering. But secondly, think about how many women are then spending money on costly treatments and simultaneously are unable to contribute to a world that desperately needs strong and passionate people. The estimated financial burden of endometriosis is $22 billion in the United States[1], yet the funding for research going into this disease according to the National Institute of Health was only $10 million last year[2]. That makes no sense. We need to stand up and say ENOUGH! Enough suffering endured by my sister, wife, girlfriend, mother or friend. I demand answers. Women battling in silence, please speak up. People who know loved ones suffering, please speak up. Talk about it, post about it or take up the yellow challenge by posting a yellow photo every day this month. Until we create a conversation loud enough to be heard by those in a position to fund research, there will be no change to the archaic diagnosis and treatment methods currently being used.

Natalie xx

P.S. If there are any women who believe they have a few of the endometriosis symptoms or have received ineffective treatment, please contact me and I would be happy to try and help you on your journey.

[1] Simoens, S., Hummelshoj, L., & D’Hooghe, T. (2007). Endometriosis: cost estimates and methodological perspective. Human reproduction update,13(4), 395-404.