Guide

Perimenopause and hormonal health: the functional medicine assessment

Perimenopause is the years of fluctuating hormones before periods stop, and it is diagnosed on symptoms, not blood tests. A functional medicine assessment adds what a standard review leaves out: thyroid, iron, blood sugar, sleep, and cardiovascular and cognitive risk. I offer it in London and online, alongside HRT rather than instead of it.

What perimenopause actually is

Perimenopause is not low oestrogen. That is the misunderstanding behind most of the poor advice, and most of the unhelpful testing, in this area.

It is the transition, usually starting in the early to mid forties and lasting anywhere from a couple of years to nearly a decade, during which the ovaries become less predictable. Progesterone falls first, because cycles without ovulation become more common, and a cycle without ovulation produces no progesterone at all. Oestrogen does not decline smoothly. It swings, often to levels higher than earlier in life before crashing, and the swings produce many of the symptoms. Menopause itself is a single day, twelve months after the last period. Everything before it is perimenopause, and everything after it is postmenopause.

The consequence for testing is direct. A blood test measures one moment in a system that is fluctuating week to week. NICE guideline NG23, updated in November 2024, says that in women over forty-five perimenopause and menopause should be diagnosed on symptoms alone, without laboratory tests. Between forty and forty-five, an FSH test may be considered; under forty, where premature ovarian insufficiency is the concern, two FSH levels taken weeks apart are needed. Anyone offering you a hormone panel to 'confirm' perimenopause at forty-eight is either unaware of the guidance or ignoring it.

The symptoms are wider than hot flushes, and the ones that bring people to me are usually the others:

  • Sleep that breaks at three or four in the morning, with or without night sweats
  • Anxiety, low mood, irritability, or a loss of resilience that feels unlike you
  • Brain fog: word-finding, concentration, holding a thread. This is the symptom that frightens people, and the one most often mistaken for early dementia
  • Joint and muscle aches, sometimes labelled fibromyalgia
  • Palpitations, which are frequently investigated by cardiology and found to be nothing cardiac
  • New or changed migraine
  • Heavier, closer or more erratic periods, and the iron deficiency that follows
  • Weight gain around the middle despite no change in habits, and rising cholesterol
  • Vaginal dryness, urinary symptoms and recurrent urinary infections
  • Loss of libido

Several of those are also the symptoms of thyroid disease, iron deficiency, sleep apnoea, insulin resistance and depression, all of which become more common in the same decade. That overlap is the reason a symptom checklist is not enough on its own, and it is the reason for the assessment below.

What a functional medicine assessment covers that a standard review does not

A good GP menopause review, done according to NICE, covers symptoms, medical history, contraception, cardiovascular risk and a discussion of HRT. Where it is done well it is excellent. Where it goes wrong is usually one of two ways: a ten-minute appointment in which the symptoms are attributed to stress, or a prescription for HRT with nothing else looked at, so that the woman who is also hypothyroid, iron deficient and not sleeping stays unwell and concludes HRT does not work.

What I do is longer and wider. The table sets out the difference honestly, including the tests I do not think earn their place.

Standard review versus a functional medicine assessment
AreaStandard GP reviewWhat I addWhy
DiagnosisClinical, on symptoms (correctly)The same. I do not use hormone panels to diagnose perimenopause over 45.NICE NG23. Levels fluctuate too much to be useful.
ThyroidTSH, sometimes free T4Free T3 and thyroid antibodies as wellAutoimmune thyroiditis peaks in this decade and produces the same symptoms. TSH alone misses early disease.
IronHaemoglobin, perhaps ferritinFerritin with transferrin saturation and CRPHeavy perimenopausal bleeding drains iron. A ferritin in the low-normal range still produces fatigue, hair loss and poor concentration.
Blood sugarHbA1c if at riskFasting insulin and glucose, HbA1c, lipids with ApoBFalling oestrogen worsens insulin sensitivity. This is the decade in which cardiovascular risk in women rises fastest.
NutrientsRarelyVitamin D, B12 with methylmalonic acid, folate, red cell magnesium, omega-3 indexCommon deficiencies, cheap to correct, each with a plausible link to the symptoms.
SleepAsked aboutStructured history and sleep apnoea screeningApnoea in women rises sharply after menopause and is under-diagnosed because it presents as fatigue and low mood, not snoring.
Stress physiologyAsked aboutMorning cortisol and DHEA-S where the history warrantsA blunted or exaggerated pattern changes how I sequence treatment. I do not use the label adrenal fatigue; it is not a diagnosis.
AndrogensRarelyTestosterone and SHBG where libido or energy are the main complaintRelevant to the discussion of testosterone, which the British Menopause Society supports for low sexual desire when HRT alone has not helped.
BoneFRAX if risk factorsDEXA referral where risk is raisedBone loss accelerates in the years around menopause. Early knowledge changes decisions.
Cognitive and cardiovascular riskQRISK if requestedHomocysteine, hs-CRP, ApoB, lipoprotein(a); ApoE genotype where there is a family history of dementiaWomen carrying ApoE4 appear to be more affected by the timing of menopause and hormone therapy. My main clinical interest is cognitive decline, and this is where the two meet.
GutRarelyStool analysis or breath testing only where there are digestive symptomsNot routine. Ordered when there is a reason.

Where HRT fits, and what sits alongside it

The evidence for HRT has been through a long correction since the Women's Health Initiative results of 2002 frightened a generation of women and doctors away from it. The re-analyses of that trial, and the guidance that followed, support a clearer position: for most women under sixty, or within ten years of menopause, the benefits of HRT for symptoms outweigh the risks, and the risks are smaller than was believed. NICE NG23 recommends HRT as the first-line treatment for hot flushes and night sweats, and the 2024 update added cognitive behavioural therapy as an option alongside or instead of it, for vasomotor symptoms, sleep and mood.

The modern regimens matter. Transdermal oestradiol, as a patch, gel or spray, does not carry the increased clotting risk of oral oestrogen. Micronised progesterone is better tolerated and appears safer for the breast than the older synthetic progestogens. Vaginal oestrogen for genitourinary symptoms is safe for almost everyone and can be used long-term. Testosterone, off-licence in the UK but supported by the British Menopause Society, has a place for low sexual desire that persists on HRT.

I do not position myself as your HRT prescriber. That decision belongs with you and your GP or a menopause specialist, and it should be made with your full history in front of them. What I do is the rest of it, and I will write to your GP with what I have found so that the HRT decision is made with the whole picture.

The rest of it is where much of the difference lies for the women who come to me on HRT and still not well. In rough order of how often it matters:

  1. Sleep. Nothing else works well while sleep is broken. Vasomotor symptoms disrupting sleep are the clearest indication for HRT, but apnoea, alcohol, late eating and an evening of screens are frequently doing as much damage.
  2. Iron, thyroid and vitamin D, corrected properly rather than nudged.
  3. Insulin sensitivity. Protein at every meal, resistance training two or three times a week, fewer refined carbohydrates, and a modest overnight fasting window. This is the intervention with the widest benefit: weight, energy, mood, cholesterol and long-term brain health.
  4. Alcohol. It worsens flushes, sleep, mood and breast cancer risk, and tolerance falls in this decade. I am not going to lecture you, but I will be honest about it.
  5. Strength. Muscle and bone both decline faster after menopause, and resistance training is the only intervention that reliably slows both. It also improves insulin sensitivity and mood.
  6. Targeted supplementation where a deficiency was found, and a small number of supplements with reasonable evidence for specific symptoms. I will tell you which have evidence and which are being sold to you.
  7. Non-hormonal options for women who cannot or do not want to take HRT: CBT, certain antidepressants at low dose for flushes, and newer non-hormonal drugs acting on the brain’s temperature control, which your GP or specialist can discuss.

The cognitive and long-term angle

My main clinical work is in cognitive decline and the Bredesen Protocol, and it shapes how I see this decade. Two-thirds of people with Alzheimer's disease are women, and that is not fully explained by women living longer. The loss of oestrogen at menopause changes brain energy metabolism, and the years around it are a window in which vascular risk, insulin resistance, sleep and inflammation are all shifting at once.

The evidence on whether HRT protects the brain is genuinely mixed and depends heavily on timing: started around the menopause it appears neutral or possibly protective; started many years later it may be harmful. I will not overstate it. What I will say is that a woman in her late forties with brain fog, poor sleep, rising insulin and a parent with dementia has a set of modifiable risks that deserve attention now, whatever she decides about HRT, and that the brain fog itself almost always improves when the rest is dealt with.

Where there is a family history and the worry is real, I extend the assessment along the lines set out in the early Alzheimer's guide.

Who this suits

This assessment is a good fit if you are:

  • In your forties or fifties with symptoms that have been attributed to stress, or that have not been explained
  • On HRT, and better, but not well
  • Unable or unwilling to take HRT and wanting a serious plan that is not just endurance
  • Worried about brain fog or memory, particularly with a family history of dementia
  • Told your bloods are normal, when nobody has looked beyond the basics
  • Wanting one longer appointment with a doctor who will look at the whole picture and write it down

It is a poor fit if you want a hormone panel to confirm a diagnosis, a supplement protocol in place of HRT, or a practitioner who will tell you that HRT is dangerous. I will not do any of those.

Perimenopause and hormonal health are assessed under my functional medicine service. The initial consultation is two hours; fees and what is included are on the fees page. Testing is additional and I give a written estimate before anything is ordered. I see patients in Twickenham and Richmond, and online across the UK, and a discovery call costs nothing.

Common questions

Is there a private clinic in London that takes an evidence-based approach to perimenopause?

Yes. I am a GMC-registered doctor and certified functional medicine practitioner in Twickenham, south west London, and I work to NICE NG23 and British Menopause Society guidance. That means diagnosing on symptoms, supporting HRT where it is appropriate, and assessing the thyroid, iron, metabolic, sleep and cognitive factors that a standard review leaves out.

Do I need a blood test to confirm perimenopause?

Not if you are over forty-five. NICE says the diagnosis is clinical, based on symptoms and cycle changes, and that hormone levels fluctuate too much to be useful. Between forty and forty-five an FSH test may help; under forty, two FSH levels are needed to assess for premature ovarian insufficiency.

Do you prescribe HRT?

The HRT decision is best made with your GP or a menopause specialist who will manage it long-term, and I do not position myself as that prescriber. My role is everything around it: making sure nothing else is driving your symptoms, and giving your prescriber the full picture in writing.

I am on HRT and still exhausted. What am I missing?

In my experience, most often one of iron deficiency, thyroid disease, sleep apnoea, insulin resistance or simply an HRT dose or route that has not been optimised. Each of those is identifiable and each is treatable, and the assessment is designed to find them.

Is brain fog in perimenopause a sign of early dementia?

Almost never at this age, and it usually improves substantially when sleep, hormones, iron and blood sugar are addressed. The exception is a strong family history or an unusual pattern, where I extend the assessment. The worry itself is reasonable and I take it seriously.

Are DUTCH or saliva hormone tests worth having?

I do not think so for diagnosing perimenopause or for adjusting HRT, and neither NICE nor the British Menopause Society supports them for those purposes. If you have already had one I will look at it, but I will not base treatment decisions on it.

What does the assessment cost?

It is a two-hour functional medicine consultation; the fee is on the fees page along with follow-up fees and what is included. Testing is charged separately and I give a written estimate before anything is ordered.

Discuss your case with Dr Greenland

A short discovery call is the usual starting point. It costs nothing, and it is the fastest way to find out whether this approach fits your situation.