Nutrient pathways
Exploring variants relevant to the handling of selected nutrients, with dietary intake and appropriate clinical assessments guiding practical choices.
Your body has been giving you clues for years. Let’s understand what they may be telling you.
An eight-month, practitioner-led programme with comprehensive DNA testing included. We explore selected findings across nutrition, hormone-related pathways, stress, caffeine metabolism and exercise, then interpret what is relevant alongside your history, symptoms, bloodwork and everyday experience. The result is a more considered way to approach how you eat, recover, move and look after yourself.
Perhaps you've always noticed how a late coffee affects you, how training feels different depending on your recovery, or how digestion changes during a stressful week. These are observations worth paying attention to.
In my clinical experience, one of the most fascinating moments is when a woman recognises something from her own life in the findings we explore together. A result may offer context for a pattern she's noticed for years. Sometimes it gives us a new question to investigate. For some clients, learning to trust those observations alongside a more detailed clinical picture has genuinely changed how they approach their health.
Your included test examines selected genetic variants across numerous physiological pathways. I review the findings with you, assess how strong and relevant the evidence is, and combine that information with your symptoms, bloodwork, nutrition and lifestyle. We then focus on changes that are appropriate and realistic for you.
Your report can explore a remarkable range of topics, from nutrient and caffeine metabolism to research on stress-related pathways, inflammation, hormones and exercise. Together we'll work out which parts are relevant, what still needs investigating and how to make sensible changes to your routine.
Exploring variants relevant to the handling of selected nutrients, with dietary intake and appropriate clinical assessments guiding practical choices.
Understanding possible differences in caffeine metabolism and bringing these insights into your individual habits and symptoms.
Reviewing selected genetic findings alongside metabolic markers, food preferences and the strategies that work in daily life.
Discussing relevant pathways without allowing genetics to overshadow sleep, workload, environment and psychological wellbeing.
Personalising your nutrition and exercise approach using real-world goals, progress and recovery, with genetics as one potential input.
Turning the information that is meaningful for you into manageable decisions, regular reviews and a plan you understand.
The clinical usefulness of genetic markers varies considerably. DNA results do not establish a diagnosis, determine an ideal diet or predict an individual response to exercise.
Genetic reports can be dense, sometimes contradictory and difficult to translate into everyday life. The value of this programme lies in interpreting what is relevant, understanding what isn't, and applying it alongside the clinical picture we build together.
Health history, symptoms, goals and baseline habits.
Included DNA testing and relevant clinical context.
Nutrition, exercise and lifestyle recommendations.
Ongoing assessment and practical refinements.
Perhaps you've spent years noticing patterns in your energy, appetite, response to coffee, sleep or recovery, without knowing what to make of them. You may be curious about how those experiences relate to your wider physiology and whether a more personalised strategy could help.
You'll have a practitioner to interpret the information with you, monitor how you're responding and help build a realistic approach that can evolve over time.
Imagine understanding why a certain habit may deserve a closer look, knowing which blood tests or symptoms to review, and feeling more confident adjusting your food, training, sleep routine or stress-management strategies. That's the experience I want women to have through this programme: guided interpretation, more informed decisions and a plan that responds to the individual in front of me.
Your DNA assessment is a substantial part of the investment, and it comes with eight months of personalised practitioner care. We connect relevant findings with your symptoms, lifestyle and progress, refining your plan as we learn more about you.
A comprehensive genetic report exploring selected markers across nutrition, digestion, stress and cognitive pathways, hormone support, inflammation, and cardiovascular health and exercise. Your results receive individual practitioner interpretation, with clinical relevance prioritised over impressive-looking data.
Dedicated 1:1 Zoom sessions to discuss findings, review progress and refine your recommendations.
Ongoing nutrition support that considers your symptoms, preferences, routine and response over time.
Training guidance for your experience, goals, recovery and capacity, at home or in the gym.
A structured exploration of the findings and the wider physiology behind each theme.
Educational materials, progress tools and individually considered supplement recommendations where appropriate.
These are the eight learning themes within your programme. Testing and care are personalised; the topics are educational rather than a promise that a particular genetic variant will explain a symptom or determine a treatment.
Food tolerance, nutrient intake and digestive context.
Nutrient metabolism and the foundations of energy.
Relevant pathways viewed alongside your hormonal history.
Caffeine handling, sleep and everyday stressors.
Environmental and lifestyle contributors to health.
Practical training decisions guided by more than DNA.
Foundational education on DNA maintenance and health.
Making sensible, evidence-informed lifestyle choices.
Eight months of DNA-informed education, individualised nutrition and exercise programming, monthly consultations and regular reviews, with your included genetic testing.
Eight-month programme · Enrolment terms provided before joining
Want to make sure this is the right level of care? We can talk through what you'd like to achieve on a complimentary discovery call.
Book a discovery callYes. Genetic testing is included within the eight-month programme. The exact panel and testing logistics are confirmed as part of your enrolment.
It may reveal useful associations and questions to explore, but common variants cannot reliably prescribe one perfect diet, sleep routine or workout. We interpret the evidence carefully and use your actual symptoms, bloodwork, preferences and response to different strategies to guide personalised decisions.
The programme includes monthly private consultations, fortnightly check-ins and meal-plan updates, personalised exercise guidance, educational materials and monthly interpretation of the programme's genetics themes.
We can consider your health history and whether DNA-informed education would add value. Some concerns require medical investigation or a different InHer programme. A discovery call can help identify the most appropriate starting point.
Choose “Join the Genetic Programme” to open the secure Debit Success enrolment form, or book a complimentary discovery call if you'd like to discuss suitability first.
Get started today before this once in a lifetime opportunity expires.