Our is to eliminate disparities and provide genetic services and personalized medication for the prevention of cancer and other disease. We are committed to continuously expanding our network of practitioners and offering opportunities to develop, enhance, and support their patients.
We offer four non-invasive genetic buccal swabs/mouth rinses:
Committed to scientific integrity, patient support services, patient advocacy, education and mentoring of experienced and inexperienced medical staff, GMCM’ purpose is to aid the planning, development, implementation and evaluation of standard of care for all patients receiving genetic services for personalized preventative care.
GMCM is located in a private practice in downtown Chicago, Illinois with over 30 years of combined experience in clinical research. GMCM is culturally competent and maintains the highest ethical standards with sensitivity to diverse social, religious and cultural beliefs. This has allowed GMCM to overcome the many challenges of diversified recruitment of patients and physicians.
The commitment to the development and maintenance of a healthy community has allowed GMCM to develop the Strategic Holistic Ongoing Partnership (SHOP) Program. This community outreach program identifies health needs and provides ongoing education, training and services to the healthcare professional as well as the community at large.
GMCM conducts evidence-based services that yield quality data/results, which ultimately provides the physician and any healthcare organization with a comprehensive service plan for their patients. GMCM embraces the importance of diversity in a clinical environment, while enhancing the quality of life for all populations who benefit from personalized preventative care.
Our pharmacogenomics (PGx) test addresses the inefficiencies of trial-and-error medicine by analyzing how individual genetic differences influence drug response and metabolism. Physicians use this detailed report to tailor medications according to the patient's unique metabolic profile. With the support of a dedicated PharmD hotline, both patients and physicians can address any queries or concerns regarding medication adjustments.
We offer a carrier screening analyzing 62 genes associated with 24 common hereditary diseases. This screening targets those in their prime reproductive years (18-45) and gauges the risk of passing diseases to offspring. Beyond assessing inherited disease risks, it offers insights into one's genetic composition—valuable for family planning, understanding hereditary roots, and learning about potential health concerns.
Research indicates that 10% of cancers arise from hereditary factors passed across generations. Our genetic test evaluates 31 genes associated with 8 hereditary cancers to determine an individual's risk. By discerning these risks, patients can proactively manage and potentially mitigate the onset of cancer, fostering early intervention and better outcomes.
Our non-invasive genetic test identifies mutations causing early atherosclerosis. By analyzing genes affecting plasma lipid levels and blood sugar, it pinpoints conditions heightening cardiovascular risk. Early detection is pivotal; certain conditions signify grave risk without timely treatment. For qualifying patients, chances of spotting a causative mutation can be between 60% and 80%.
People at a higher risk for cancer may have the option of having more frequent cancer screenings, avoiding specific risk factors, making lifestyle changes to lessen additional risk, taking preventive medication (chemoprevention), and/or having risk reducing surgeries in order to reduce their risk. Cancer screening panel includes:
Hereditary Breast Cancer
Breast cancer is the most common female cancer, affecting approximately 1 in 8 women in the United States. Approximately 5-10% of breast cancers are hereditary. Hereditary cancers are caused by a mutation in a gene that can be passed on from generation to generation. Women who have an abnormal mutation can have up to an 87% risk of being diagnosed with breast cancer during their lifetimes.
Factors that may increase your risk of Breast cancer include:
How to reduce the risk of Breast cancer:
Hereditary Ovarian Cancer
Ovarian cancer is the ninth most common cancer in women, but it ranks fifth as the cause of cancer death in women. While most ovarian cancer does not run in the family, approximately 10-15% of ovarian cancer is hereditary. Hereditary cancers are caused by a mutation in a gene that can be passed on from generation to generation. Women who have an abnormal mutation can have up to a 44% risk of being diagnosed with ovarian cancer during their lifetimes.
Factors that may increase your risk of Ovarian cancer include:
How to reduce the risk of Ovarian cancer:
Hereditary Colorectal Cancer
Colorectal cancer is cancer that starts in either the colon or the rectum. Most Colorectal cancer does not run in the family, but approximately 5% of colorectal cancer is hereditary. Hereditary cancers are caused by a mutation in a gene that can be passed from generation to generation. Women who have an abnormal mutation can have up to an 80% risk of being diagnosed with colorectal cancer during their lifetimes. Therefore, it is important for practitioners to talk to patients about family history of colorectal cancer and discuss undergoing regular screenings to catch any potential issues early.
Factors that may increase your risk of Colon cancer include:
How to reduce the risk of Colon cancer:
Hereditary Pancreatic Cancer
Approximately 1 in 76 people will develop pancreatic cancer in their lifetime. Most pancreatic cancer develops by chance and does not run in families. However, some pancreatic cancers are hereditary. Hereditary cancers are caused by a mutation in a gene that can be passed on from generation to generation and cause up to 10% of pancreatic cancers. Women who have an abnormal mutation can have up to a 70% risk of being diagnosed with pancreatic cancer during their lifetimes. Therefore, if you have a family history of pancreatic cancer or any other hereditary cancer, it is important to talk to your doctor and consider genetic testing to assess your risk.
Factors that may increase your risk of pancreatic cancer include:
How to reduce the risk of Pancreatic cancer:
Endometrial Cancer
Endometrial cancer, which is cancer of the lining of the uterus, is the most common cancer of the female reproductive organs. It affects approximately 1 in 41 women. While most cases of endometrial cancer are not hereditary, between 1-5% of cases are caused by a genetic predisposition. It is important to be aware of this hereditary risk if there is a family history of endometrial cancer, as it can help with early detection and prevention. Regular check-ups and screenings can also help catch endometrial cancer early on when it is more treatable.
Factors that may increase your risk of Endometrial cancer include:
How to reduce the risk of Endometrial cancer:
Gastric Cancer
Gastric cancer, also known as stomach cancer, is a type of cancer that begins in the stomach. While most cases of stomach cancer are not hereditary, some gene abnormalities can increase the risk of developing one or more types of gastric cancers.
Factors that may increase your risk of Gastric cancer include:
How to reduce the risk of Gastric cancer:
Skin Cancer
Skin cancer is a type of cancer that starts in the skin. It is divided into two main categories: non-melanoma and melanoma. Non-melanoma skin cancers, which include basal cell carcinoma and squamous cell carcinoma, are the most common types of skin cancer and are generally less dangerous than melanoma. However, melanoma is a much more aggressive form of skin cancer that can spread rapidly to other parts of the body if not detected and treated early. It is important to protect your skin from the sun's harmful UV rays by wearing protective clothing, using sunscreen, and avoiding prolonged exposure to the sun during peak hours.
Factors that may increase your risk of Skin cancer include:
How to reduce the risk of Skin cancer:
Prostate Cancer
Prostate cancer is the second most common type of cancer found in men, after skin cancer. It is estimated that 1 in every 8 men will develop prostate cancer during their lifetime. While most cases of prostate cancer occur by chance and do not have a hereditary component, a small percentage of prostate cancers are caused by inherited genetic mutations. Men who have a family history of prostate cancer or who carry certain genetic mutations, such as BRCA1 or BRCA2, are at an increased risk of developing the disease. In its early stages, prostate cancer may not cause any noticeable symptoms, which is why regular screenings are important for early detection. Men over the age of 50, African American men, and men with a family history of prostate cancer are at a higher risk of developing the disease and should talk to their healthcare provider about screening options.
Factors that may increase your risk of Prostate cancer include:
How to reduce the risk of Prostate cancer:
Select the disease and the specific condition for more detailed information.
AORTIC DYSFUNCTION OR DILATION >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
AORTIC DYSFUNCTION OR DILATION List Item 1CYSTIC FIBROSIS & CF-RELATED DISORDERS >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
CYSTIC FIBROSIS & CF-RELATED DISORDERS List Item 2NON-SYNDRONIC HEARING LOSS >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
NON-SYNDRONIC HEARING LOSS List Item 3USHER SYNDROME >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
USHER SYNDROME List Item 4SPINAL MUSCULAR ATROPHY >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
SPINAL MUSCULAR ATROPHYMAPLE SYRUP DISEASE >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
MAPLE SYRUP DISEASEFANCONI ANEMIA >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
FANCONI ANEMIALONG Q-T SYNDROME >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
LONG Q-T SYNDROMEList Item 1 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
AORTIC DYSFUNCTION OR DILATION List Item 1List Item 2 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
CYSTIC FIBROSIS & CF-RELATED DISORDERS List Item 2List Item 3 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
NON-SYNDRONIC HEARING LOSS List Item 3List Item 4 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
USHER SYNDROME List Item 4New List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
SPINAL MUSCULAR ATROPHYNew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
MAPLE SYRUP DISEASENew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
FANCONI ANEMIANew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
LONG Q-T SYNDROMENIEMANN PICK DISEASE >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
NIEMANN PICK DISEASE List Item 1TAY-SACHS >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
TAY-SACHS List Item 2CANAVAN DISEASE >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
CANAVAN DISEASE List Item 3SICKLE CELL DISEASE >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
SICKLE CELL DISEASE List Item 4GAUCHER DISEASE >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
GAUCHER DISEASEPHENYLKETONURIA >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
PHENYLKETONURIAGLYCOGEN STORAGE DISEASE >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
GLYCOGEN STORAGE DISEASEBLOOM SYNDROME >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
BLOOM SYNDROMEList Item 1 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
NIEMANN PICK DISEASE List Item 1List Item 2 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
TAY-SACHS List Item 2List Item 3 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
CANAVAN DISEASE List Item 3List Item 4 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
SICKLE CELL DISEASE List Item 4New List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
GAUCHER DISEASENew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
PHENYLKETONURIANew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
GLYCOGEN STORAGE DISEASENew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
BLOOM SYNDROMEALPHA THALASEMIA >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
ALPHA THALASEMIA List Item 1BETHA THALASEMIA >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
BETHA THALASEMIA List Item 2MUCOLIPIDOSIS TYPE IV >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
MUCOLIPIDOSIS TYPE IV List Item 3FAMILIAL DYSAUTONOMIA >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
FAMILIAL DYSAUTONOMIA List Item 4GLYCOGEN STORAGE DISEASE II >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
GLYCOGEN STORAGE DISEASE IICLASSICAL GALACTOSEMIA >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
CLASSICAL GALACTOSEMIAORNITHINE TRANSCARBAMYLASE DEFICIENCY >> Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
ORNITHINE TRANSCARBAMYLASE DEFICIENCYList Item 1 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
ALPHA THALASEMIA List Item 1List Item 2 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
BETHA THALASEMIA List Item 2List Item 3 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
MUCOLIPIDOSIS TYPE IV List Item 3List Item 4 Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
FAMILIAL DYSAUTONOMIA List Item 4New List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
GLYCOGEN STORAGE DISEASE IINew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
CLASSICAL GALACTOSEMIANew List Item Write a description for this list item and include information that will interest site visitors. For example, you may want to describe a team member's experience, what makes a product special, or a unique service that you offer.
ORNITHINE TRANSCARBAMYLASE DEFICIENCYPerforming the following steps during patient initial intake will be the most efficient. The total time required is approximately 3-5 minutes from start to finish.
PATIENT SCREENING AND SAMPLE COLLECTION
Every day, our clinic staff screens and identifies suitable patients. Trained professionals within the clinic discuss the test, ensuring informed consent, and then collect a mouth swab sample. Before dispatching, patient identification and insurance details are verified. All samples are shipped as per the provided guidelines, using the designated prepaid package.
TEST MATERIALS AND BENEFITS
GreenMCMeds supplies all required materials for swabs and mouth rinses, supplemented by promotional literature. Physicians benefit from this zero-start-up-cost service. Moreover, these tests are pivotal in refining clinical judgment, facilitating a comprehensive, precise treatment strategy, and ultimately elevating the patient's quality of life.
A positive test result means that the patient has the mutation and is at higher risk than the average patient for particular gene. It does not guarantee the patient will inherit the disease or will in fact get cancer.
A negative test result means that the patient doesn’t have a particular mutation that will affect the patient. It doesn’t mean you will not get the cancer/disease, it just means IF you do, it was not genetically related and was caused by environmental or social reasons.
The patient is pre-screened and goes through a prior authorization with the patient’s insurance to identify if the patient qualifies for 100% coverage. If the patient has any financial responsibility towards their test sample, they are contacted directly to offer financial payment options or can opt out at anytime prior to the laboratory running the sample to prevent getting billed.
There are absolutely no start up costs for a physician, clinic or organization to offer these services to their patients. GreenMCMeds provides all kits, marketing material and pre-paid shipping packaging labels to mail samples to our testing laboratory.
Depending on the clinics supporting staff, either the physician, or the appointed staff will identify qualified patients for the day based on family history, and/or insurance coverage from a provided accepted insurance list for that specific test. Upon a successful candidate list for the screening assessment service, explain the service being offered to the patient during the encounter, gather patient/physician signatures (Requisition/Consent Forms), make/print copy of patient’s insurance and perform the mouth swab/rinse on patient.
Mon Chéri remains a profound source of inspiration for us. Her courageous battle with brain cancer compelled us to reassess our approach to illness and disease, prescription drugs, and the critical significance of knowledge in both preventing and treating them. Additionally, her journey ignited our passion for plant science and its potential to heal not only individuals but also the world at large, driving us to explore innovative ways to harness the power of nature for holistic health and environmental sustainability.
Collaboration with CC Insurance
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