MTHFR Treatment in Raleigh, North Carolina
Methylation and the MTHFR gene mutation have received significant attention in recent years due to their impact on health.
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At FoundationMED in Raleigh, North Carolina, we specialize in MTHFR treatment, identifying genetic mutations and optimizing methylation processes through personalized therapy.
Understanding MTHFR and Methylation
Methylation is a biochemical process that transfers a methyl group from one substance to another. This essential function enables biological processes, including:
- Detoxification
- DNA repair and synthesis
- Neurotransmitter production
- Energy metabolism
- Immune system regulation
The MTHFR gene (methylenetetrahydrofolate reductase) plays a key role in converting homocysteine into methionine, an amino acid essential for building proteins. MTHFR mutations can impair this process, increasing the risk of various health issues.
Symptoms of MTHFR Gene Mutation
Individuals with MTHFR mutations may experience:
- Chronic fatigue
- Depression and anxiety
- Migraines
- Insomnia
- Digestive issues
- Cardiovascular disorders
- Fibromyalgia or chronic pain
- Increased inflammation
Since MTHFR mutations affect methylation efficiency, they can contribute to neurological, cardiovascular, and immune-related disorders.
Diagnosing MTHFR Gene Mutation
At FoundationMED, we use comprehensive genetic testing to assess MTHFR status. Our evaluation includes:
- Genetic testing to identify MTHFR mutations.
- Homocysteine level testing to measure methylation efficiency.
- Comprehensive blood panels to check for vitamin and nutrient deficiencies.
- Gut health assessment to evaluate digestion and detoxification efficiency.
- Toxin burden analysis to identify environmental factors affecting methylation
By understanding your MTHFR status, we can develop a personalized therapy plan to optimize methylation and support overall health.
MTHFR Treatment Options
Nutritional and Supplement Therapy
Since MTHFR mutations can affect the body's ability to process folate, we focus on targeted nutritional therapy, which includes:
- Methylated B vitamins (B12 and folate) to support proper methylation.
- Magnesium and zinc to enhance enzyme function.
- Antioxidants (glutathione, vitamin C, and NAC) to reduce oxidative stress.
- Omega-3 fatty acids to reduce inflammation and improve cardiovascular health.
- Probiotics to support gut microbiome balance, essential for methylation.
Lifestyle Modifications
Since methylation efficiency is influenced by more than genetics, our MTHFR therapy includes:
- Detoxification protocols to eliminate heavy metals and environmental toxins.
- Stress management techniques like meditation and deep breathing to lower cortisol levels.
- Adequate sleep strategies to support optimal genetic expression.
- Dietary changes focused on whole, organic foods to reduce synthetic folic acid intake.
Functional and Medical Interventions
For individuals experiencing severe symptoms related to MTHFR gene mutation, additional interventions may be necessary:
- Hormone balancing therapy to support neurotransmitter production.
- GI health optimization to enhance nutrient absorption.
- Bioindividual treatment plans based on genetic expression and metabolic function
Each treatment plan is customized to address MTHFR-related challenges, helping patients achieve optimal health.
Preparing for Your Appointment
Before your consultation, take note of any symptoms, diet, and environmental exposures that may impact methylation. Our specialists at FoundationMED will conduct a thorough evaluation to determine the most effective MTHFR treatment for your needs.
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What Our have To Patients Say
FoundationMED always appreciates feedback from our valued patients. We’re thrilled to have an average rating of 5 out of 5 stars. Please read what others are saying about us below, and as always, we would love to collect your feedback.
BOOK APPOINTMENT“I was fortunate to have participated in a group coaching program with Sharon Fowler. The overall experience was enjoyable and insightful. I loved the group chats and individual assessments and learned a lot about vision and goal setting as well as making habit changes.”
“I was fortunate to have participated in a group coaching program with Sharon Fowler. The overall experience was enjoyable and insightful. I loved the group chats and individual assessments and learned a lot about vision and goal setting as well as making habit changes.”
Frequently Asked Questions
MTHFR testing involves genetic blood or saliva tests to identify mutations in the MTHFR gene. Additional blood work may assess homocysteine and folate levels.
MTHFR mutations are relatively common, with about 30-50% of the population carrying at least one mutation. However, the impact varies based on individual health factors.
Individuals with MTHFR mutations may experience chronic fatigue, anxiety, depression, migraines, and inflammation. Genetic testing is the only way to confirm MTHFR status.
MTHFR treatment focuses on methylated B vitamins, nutritional support, detoxification, and lifestyle changes to optimize methylation and reduce health risks.
MTHFR mutations affect a significant portion of the population, but not everyone with a mutation experiences health problems. The impact depends on other genetic and environmental factors.
