Sierra Acai Company
Sierra Acai Company
Open 7 Days a Week
MonaVie Independent Distributor
Distributor Training
Shop Online
Enroll Now
Buy Wholesale and maintain an Active status for 2 months and we will refund your $39 Distributor Fee
Friends
Buy Wholesale and maintain an Active status for 2 months and we will refund your $39 Distributor Fee
07-SEPTEMBER-2008 03:17:44 - Creutzfeldt-Jakob disease Creutzfeldt-Jakob disease Classification and external resources ICD-10 A81.0, F02.1 ICD-9 046.1 OMIM 123400 DiseasesDB 3166 eMedicine neuro/725 MeSH D007562 Creutzfeldt-Jakob-Stortz disease CJD is a very rare and incurable degenerative neurological disorder brain disease that is ultimately fatal.1 Among the types of transmissible spongiform encephalopathy found in humans, it is the most common.citation needed Contents 1 History 2 Causes 3 Incidence and prevalence 3.1 New concerns on incidence and prevalence 4 Symptoms 5 Diagnosis 6 Treatment 7 Transmission 7.1 Blood donor restrictions 8 Cultural references 9 References 10 External links History The disease was first described by German neurologists, Hans Gerhard Creutzfeldt and Alfons Maria Jakob, in 1920. Some of the clinical findings described in their first papers do not match current criteria for Creutzfeldt-Jakob disease, and it is considered highly likely that at least two of the patients in initial studies were suffering from a different ailment. Causes Transmissible spongiform encephalopathy diseases are caused by prions. The diseases are thus sometimes called prion diseases. Other prion diseases include Gerstmann-Sträussler-Scheinker syndrome GSS, fatal familial insomnia FFI and kuru in humans, as well as bovine spongiform encephalopathy BSE, commonly known as mad cow disease chronic wasting disease CWD in elk and deer, and scrapie in sheep. Alpers' syndrome in infants is also thought to be a transmissible spongiform encephalopathy caused by a prion.23 The prion that is believed to cause Creutzfeldt-Jakob exhibits at least two stable conformations. One, the native state, is water-soluble and present in healthy cells. As of 2007, its biological function is presumably in transmembrane transport or signaling. The other conformational state is very poorly water-soluble and readily forms protein aggregates. People can also acquire CJD genetically through a mutation of the gene that codes for the prion protein PRNP. This only occurs in 5-10% of all CJD cases. The CJD prion is dangerous because it promotes refolding of native proteins into the diseased state. The number of misfolded protein molecules will increase exponentially,citation needed and the process leads to a large quantity of insoluble prions in affected cells. This mass of misfolded proteins disrupts cell function and causes cell death. Mutations in the gene for the prion protein can cause a misfolding of the dominantly alpha helical regions into beta pleated sheets. This change in conformation disables the ability of the protein to undergo digestion. Once the prion is transmitted, the defective proteins invade the brain and are produced in a self-sustaining feedback loop, causing exponential spread of the prion, leading to death within a few months, although a few patients have lived as long as two years. Stanley B. Prusiner of University of California, San Francisco UCSF was awarded the Nobel Prize in physiology or medicine in 1997 for his discovery of prions. For more than a decade, Yale University neuropathologist Laura Manuelidis has been challenging this explanation for the disease. In January 2007 she and her colleagues published an article in the Proceedings of the National Academy of Science and reported that they have found a virus-like particle but without finding nucleic acids so far in less than 10% of the cells a scrapie-infected cell line and in a mouse cell line infected by a human CJD agent.4 Incidence and prevalence Although CJD is the most common human prion disease, it is still rare and only occurs in about one out of every one million people. It usually affects people aged 45-75, most commonly appearing in people between the ages of 60-65. The exception to this is the more recently-recognised 'variant' CJD vCJD, which occurs in younger people. CDC monitors the occurrence of CJD in the United States through periodic reviews of national mortality data: According to the CDC: CJD occurs worldwide at a rate of about 1 case per million population per year. On the basis of mortality surveillance from 1979 to 1994, the annual incidence of CJD remained stable at approximately 1 case per million persons in the United States. In the United States, CJD deaths among persons younger than 30 years of age are extremely rare fewer than 5 deaths per billion per year.citation needed The disease is found most frequently in patients 55-65 years of age, but cases can occur in persons older than 90 years and younger than 55 years of age. In more than 85% of cases, the duration of CJD is less than 1 year median: 4 months after onset of symptoms.15 New concerns on incidence and prevalence In The Lancet June 2006, a University College London team suggested that it may take more than 50 years for vCJD to develop, from their studies of kuru, a similar disease in Papua New Guinea.6 The reasoning behind the claim is that kuru was possibly transmitted through cannibalism in Papua New Guinea when family members would eat the body of a dead relative as a sign of mourning. In the 1950s, the practice was banned, thereby preventing any further possible transmission. In the late 20th century, however, kuru reached epidemic proportions in certain Papua New Guinean communities, therefore suggesting that vCJD may also have a similar incubation period of 30 to 50 years. A critique to this theory is that while mortuary cannibalism was banned in Papua New Guinea in the 1950s, that does not necessarily mean that the practice ended. Fifteen years later Jared Diamond was informed by Papuans that the practice continued.7 There is dispute as to whether the Fore ever practiced cannibalism, due to the fact that nobody ever observed them and that Kuru could have passed to the Fore through the preparing of the dead body for burial. These researchers noticed a genetic variation in some kuru patients that has been known to promote long incubation periods. They have also proposed that individuals who contracted CJD in the early 1990s represent a distinct genetic subpopulation, with unusually short incubation periods for BSE. This means that there may be many more vCJD patients who have longer incubation periods, which may surface many years later.6 In 1997 a number of Kentuckians contracted the disease. It was discovered that all the victims had a penchant for squirrel brains.89 See: http://www.guardian.co.uk/uk/2008/aug/03/bse.medicalresearch for recent concerns. Symptoms The first symptom of CJD is rapidly progressive dementia, leading to memory loss, personality changes and hallucinations. This is accompanied by physical problems such as speech impairment, jerky movements myoclonus, balance and coordination dysfunction ataxia, changes in gait, rigid posture, and seizures. The duration of the disease varies greatly, but sporadic non-inherited CJD can be fatal within months or even weeks Johnson, 1998. In some people, the symptoms can continue for years. In most patients, these symptoms are followed by involuntary movements and the appearance of a typical diagnostic electroencephalogram tracing. The symptoms of CJD are caused by the progressive death of the brain's nerve cells, which is associated with the build-up of abnormal prion proteins. When brain tissue from a CJD patient is examined under a microscope, many tiny holes can be seen where whole areas of nerve cells have died. The word 'spongiform' in 'transmissible spongiform encephalopathies' refers to the 'spongy' appearance of the brain tissue. Diagnosis The diagnosis of CJD is suspected when there are typical clinical symptoms and signs such as rapidly progressing dementia with myoclonus. Further investigation can then be performed to support the diagnosis including Electroencephalography - often has characteristic triphasic spikes Cerebrospinal fluid analysis for 14-3-3 protein MRI of the brain - often shows high signal intensity in the caudate nucleus and putamen bilaterally on T2-weighted images. Diffusion Weighted Imaging DWI images are the most sensitive. In about 24% of cases DWI shows only cortical hyperintensity; in 68%, cortical and subcortical abnormalities; and in 5%, only subcortical anomalies.10 The involvement of the thalamus can be found in sCJD, even is stronger and constant in vCJD.11 Clinical testing for CJD has always been an issue. Diagnosis has mostly been based on clinical and physical examination of symptoms. In recent years, studies have shown that the tumour marker Neuron-specific enolase NSE is often elevated in CJD casescitation needed. In one third of patients with sporadic CJD, deposits of prion protein scrapie, PrPSc, can be found in the skeletal muscle and/or the spleencitation needed. Diagnosis of vCJD can be supported by biopsy of the tonsils, which harbour significant amounts of PrpSc; however, biopsy of brain tissue is the definitive diagnostic test. Clinical and Pathologic Characteristics:12 Characteristic Classic CJD Variant CJD Median age at death 68 years 28 years Median duration of illness 4-5 months 13-14 months Clinical signs and symptoms Dementia; early neurologic signs Prominent psychiatric/behavioral symptoms; painful dysesthesias; delayed neurologic signs Periodic sharp waves on electroencephalogram Often present Often absent Signal hyperintensity in the caudate nucleus and putamen on diffusion-weighted and FLAIR MRI Often present Often absent Pulvinar sign on MRI Not reported Present in 75% of cases Immunohistochemical analysis of brain tissue Variable accumulation. Marked accumulation of protease-resistant prion protein Presence of agent in lymphoid tissue Not readily detected Readily detected Increased glycoform ratio on immunoblot analysis of protease-resistant prion protein Not reported Marked accumulation of protease-resistant prion protein Presence of amyloid plaques in brain tissue May be present May be present An abnormal signal in the posterior thalami on T2- and diffusion-weighted images and fluid-attenuated inversion recovery sequences on brain magnetic resonance imaging MRI; in the appropriate clinical context, this signal is highly specific for vCJD. Source: CDC Treatment There is currently no cure for CJD, a fatal disease, and the search for viable treatments continues. An experimental treatment was given to a Northern Irish teenager, Jonathan Simms, beginning in January 2003.13 The medication, called pentosan polysulphate PPS and used to treat interstitial cystitis, is infused into the patient's lateral ventricle within the brain. PPS does not seem to stop the disease from progressing, and both brain function and tissue continue to be lost. However, the treatment is alleged to slow the progression of the otherwise untreatable disease, and may have contributed to the longer than expected survival of the seven patients that were studied.14 The CJD Therapy Advisory Group to the UK Health Departments advises that data are not sufficient to support claims that pentosan polysulphate is an effective treatment and suggests that further research in animal models is appropriate.15 A 2007 review of the treatment of 26 patients with PPS finds no proof of efficacy because of the lack of accepted objective criteria.16 Scientists have investigated using RNA interference to slow the progression of scrapie in mice. The RNA blocks production of the protein that the CJD process transforms into prions. This research is unlikely to lead to a human therapy for many years.17 Both amphotericin B and doxorubicin have been investigated as potentially effective against CJD, but as yet there is no strong evidence that either drug is effective. Further study has been taken with other medical drugs, but none are effective. Experiments with Cannabis are currently being undertaken. Dr. Michael Geschwind, Dr. Bruce Miller and Dr. Stanley Prusiner from University of California, San Francisco are currently running a treatment trial for sporadic CJD using quinacrine, a medicine originally created for malaria. Pilot studies showed quinacrine permanently cleared abnormal prion proteins from cell cultures, but results have not yet been published on the clinical study. Transmission The defective protein can be transmitted by human growth hormone hGH products, Immunoglobulins IVIG, corneal grafts, dural grafts or electrode implants acquired or iatrogenic form: iCJD; it can be inherited herary or familial form: fCJD; or it may appear for the first time in the patient sporadic form: sCJD. In the herary form, a mutation occurs in the gene for PrP, PRNP. 10 to 15% of CJD cases are inherited. CDC The disease has also been shown to result from usage of HGH drawn from the pituitary glands of cadavers who died from Creutzfeldt-Jakob Disease,18 though the known incidence of this cause is as of April 2004 quite small. The risk of infection through cadaveric HGH usage in the US only ceased when the medication was withdrawn in 1985. It is thought that humans can contract the disease by consuming material from animals infected with the bovine form of the disease.citation needed The only suspected cases to arise thus far have been vCJD, although there are fears - based on animal studies - that consuming beef or beef products containing prion particles can also cause the development of classic CJD.citation needed When BSE material infects humans the resulting disease is known as new variant CJD DiseasenvCJD19 Cannibalism has also been implicated as a transmission mechanism for abnormal prions, causing the disease known as kuru, found primarily among women and children of the Fore tribe in Papua New Guinea. While the men of the tribe ate the body of the deceased and were not affected, the women and children ate the brain and contracted the disease from infected brain tissue. Prions, the infectious agent of CJD, may not be inactivated by means of routine surgical instrument sterilization procedures. The World Health Organization and the US Centers for Disease Control and Prevention recommend that heat and chemical decontamination be used in combination to process instruments that come in contact with high-infectivity tissues. No cases of iatrogenic transmission of CJD have been reported subsequent to the adoption of current sterilization procedures, or since 1976.202122 Copper-hydrogen peroxide has been suggested as an alternative to the current recommendation of sodium hydroxide or sodium hypochlorite.23 Thermal depolymerization also destroys prions in infected organic and inorganic matter, since the process dissolves protein at the molecular level. Blood donor restrictions In 2004 a new report published in the Lancet medical journal showed that vCJD can be transmitted by blood transfusions.24 The finding alarmed healthcare officials because a large epidemic of the disease might arise in the near future. There is no test to determine if a blood donor is infected and in the latent phase of vCJD. In reaction to this report, the British government banned anyone who had received a blood transfusion since January 1980 from donating blood.citation needed On May 28, 2002, the United States Food and Drug Administration instituted a policy that excludes from donation anyone who spent at least 6 months in certain Western European countries, or 3 months in the United Kingdom, from 1980 to 1996. Given the large number of U.S. military personnel and their dependents residing in Europe, it was expected that over 7% of donors would be deferred due to the policy. Later changes to this policy have relaxed the restriction to a cumulative total of 5 years or more of civilian travel in Western European countries 6 months or more if military. The 3-month restriction on travel to the UK, however, has not been changed.25 The American Red Cross' policy is as follows: Since January 1, 1980-December 31, 1996 spending a total time of 3 months or more in Channel Islands, England, Falkland Islands, Isle of Man, Gibraltar, Northern Ireland, Scotland, and Wales would preclude you from donating. Since January 1, 1980 to present, spending a total time of 5 years or more in the above countries and countries in Europe. For complete listing, please go to Redcross.org A similar policy applies to potential donors to the Australian Red Cross' Blood Service, precluding people who have spent a cumulative time of six months or more in the United Kingdom between 1980 and 1996. The Singapore Red Cross precludes potential donors who have spent a cumulative time of three months or more in the United Kingdom between 1980 and 1996. In New Zealand anyone who lived in the UK, France or the Republic of Ireland for a total of six months or more between 1980 and 1996 is permanently deferred from donating blood in New Zealand As of 1999, Health Canada announced a policy to defer individuals from donating blood if they have lived within the United Kingdom for one month or more from Jan. 1, 1980 to Dec. 31, 1996. In 2000, the same policy was applied to people who have resided in France, for at least three months from Jan. 1980 to Dec. 1996. Canada will not accept blood from a person who has spent more than 6 months in a Western European country since January 1, 1980.26 The Association of Blood Donors of Denmark precludes potential donors who have spent a cumulative time of at least twelve months in the United Kingdom between 1 January 1980 and 31 December 1996. The Swiss Blutspendedienst SRK precludes potential donors who have spent a cumulative time of at least six months in the United Kingdom between 1 January 1980 and 31 December 1996. Cultural references George Balanchine, the esteemed choreographer, was found to have traces of Creutzfeldt-Jakob disease in his brain after his death. Indeed, his final years showed evidence of related symptoms.27 The disease was also featured in an episode of the X-Files, Our Town, in which a group of cannibals eat the whole body brain and all of their fellow humans in order to stay young forever. They contract the disease from one of their victims, and it passes through the whole town, killing them. During the fourth season of the TV series House, in episode four Guardian Angels House, House's job applicants suspect the patient of having contracted CJD after doing cosmetic work on a cadaver with similar symptoms at a funeral parlour. To test the diagnosis the team dig up the grave and carry out a brain biopsy, which is negative. References ^ a b CDC Classic CJD. Retrieved on 2008-04-15. ^ Chakraborty, C., Nandi, S. and Jana, S. 2005.Current Pharmaceutical Biotechnology, 6:167-177 ^ Obi, R. K. and NwanebuAfrican, F. C. 2008 Journal of Clinical and Experimental Microbiology. 91:38-52 ^ Manuelidis L; Yu ZX, Barquero N, Mullins B February 6, 2007. Cells infected with scrapie and Creutzfeldt-Jakob disease agents produce intracellular 25-nm virus-like particles. Proceedings of the National Academy of Science 104 6: 1975-1970. doi:10.1073/pnas.0610999104. PMID 17267596. Retrieved on 2007-09-24. ^ Variant CJD, Fact Sheet. Retrieved on 2007-12-02. ^ a b forbeslife. Retrieved on 2007-12-02. ^ Diamond, J.M. 2000Archaeology: Talk of cannibalism Nature 407, 25-26. ^ Berger J 1997. Creutzfeldt-Jakob Disease and eating squirrel brains. doi:10.1016/S0140-67360563333-8. ^ Explainer: Squirrel a la Huckabee. Retrieved on 2008-03-24. ^ Young, Geoffrey S.; Michael D. Geschwind, Nancy J. Fischbein, Jennifer L. Martindale, Roland G. Henry, Songling Liu, Ying Lu, Stephen Wong, Hong Liu, Bruce L. Miller and William P. Dillon June-July 2005. Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Imaging in Creutzfeldt-Jakob Disease: High Sensitivity and Specificity for Diagnosis. American Journal of Neuroradiology 26: 1551-1562. American Society of Neuroradiology. PMID 15956529. Retrieved on 2007-10-30. ^ Tschampa, Henriette J.; Petra Mürtz, Sebastian Flacke, Sebastian Paus, Hans H. Schild and Horst Urbach May 2003. Thalamic Involvement in Sporadic Creutzfeldt-Jakob Disease: A Diffusion-Weighted MR Imaging Study. American Journal of Neuroradiology 24: 908-915. American Society of Neuroradiology. PMID 12748093. Retrieved on 2007-10-30. ^ Belay ED, Schonberger LB 2002. Variant Creutzfeldt-Jakob disease and bovine spongiform encephalopathy. Clin. Lab. Med. 22 4: 849-62, v-vi. PMID 12489284. ^ Teenager with vCJD 'stable. BBC News 13 December 2004. Retrieved on 2007-01-01. ^ Bone, Ian 12 July 2006. Intraventricular Pentosan Polysulphate in Human Prion Diseases: A study of Experience in the United Kingdom. Medical Research Council. Retrieved on 2007-01-01. ^ Use of Pentosan Polysulphate in the treatment of, or prevention of, vCJD. Department of Health:CJD Therapy Advisory Group. Retrieved on 2007-10-30. ^ Rainov NG, Tsuboi Y, Krolak-Salmon P, Vighetto A, Doh-Ura K 2007. Experimental treatments for human transmissible spongiform encephalopathies: is there a role for pentosan polysulfate?. Expert opinion on biological therapy 7 5: 713-26. doi:10.1517/14712598.7.5.713. PMID 17477808. ^ Revamp of brain 'could slow CJD'. BBC News 4 December 2006. Retrieved on 2007-01-01. ^ HGH Linked to Brain Eater. Retrieved on 2007-12-02. ^ Obi, R. K. and NwanebuAfrican, F. C. 2008 Journal of Clinical and Experimental Microbiology. 91:38-52 ^ Questions and Answers: Creutzfeldt-Jakob Disease Infection-Control Practices. Infection Control Practices/CJD Creutzfeldt-Jakob Disease, Classic. Centers for Disease Control and Prevention January 4, 2007. Retrieved on 2007-06-09. ^ WHO Infection Control Guidelines for Transmissible Spongiform Encephalopathies 26 March 1999. Retrieved on 2007-06-09. ^ McDonnell G, Burke P. 2003. The challenge of prion decontamination. Clin Infect Dis 36: 1152-4. doi:10.1086/374668. ^ Solassol J, Pastore M, Crozet C, et al. 2006. A novel copper-hydrogen peroxide formulation for prion decontamination. J Infect Dis 194: 865-869. doi:10.1086/506947. ^ Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW 2004. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet 364 9433: 527-9. doi:10.1016/S0140-67360416811-6. PMID 15302196. ^ In-Depth Discussion of Variant Creutzfeld-Jacob Disease and Blood Donation. Retrieved on 2007-12-02. ^ H�ma-Qu�bec, blood, donors, blood donation, volunteers, receivers, blood drives, Globule, blood clinics, stem cells, blood cord, human tissues, safety, H�ma-Qu�bec, job openings, press center. Retrieved on 2007-12-02. ^ Gottlieb, Robert 2004. George Balanchine: the ballet maker. New York: HarperCollins/Atlas Books, 179-181. ISBN 0-06-075070-7. External links Creutzfeldt-Jakob Disease Foundation UCSF Memory and Aging Center - CJD Info The National Creutzfeldt-Jakob Disease Surveillance Unit NCJDSU in UK v d e Infectious diseases - Prion diseases / Transmissible spongiform encephalopathy A81, 046 Prion diseases in humans Creutzfeldt-Jakob disease - Kuru - Gerstmann-Sträussler-Scheinker syndrome - Fatal familial insomnia Prion diseases in animals Bovine spongiform encephalopathy - Scrapie - Chronic wasting disease - Transmissible mink encephalopathy v d e WHO ICD-10 mental and behavioral disorders F · 290-319 Neurological/symptomatic Dementia Alzheimer's disease, multi-infarct dementia, Pick's disease, Creutzfeldt-Jakob disease, Huntington's disease, Parkinson's disease, AIDS dementia complex, Frontotemporal dementia, Elopement, Sundowning, Wandering · Delirium · Post-concussion syndrome · Organic brain syndrome Psychoactive substance alcohol drunkenness, alcohol dependence, alcoholic hallucinosis, Alcohol withdrawal, delirium tremens, Korsakoff's syndrome, alcohol abuse · opioids opioid dependency · sedative/hypnotic benzodiazepine withdrawal · cocaine cocaine dependence · general Intoxication, Drug abuse, Physical dependence, Withdrawal Psychotic disorder Schizophrenia disorganized schizophrenia · Schizophreniform disorder · Schizotypal personality disorder · Delusional disorder · Folie à deux · Schizoaffective disorder Mood affective Mania · Bipolar disorder · Clinical depression · Cyclothymia · Dysthymia Neurotic, stress-related and somatoform Anxiety disorder Agoraphobia, Panic disorder, Panic attack, Generalized anxiety disorder, Social anxiety, Social phobia · OCD · Acute stress reaction · PTSD · Adjustment disorder · Conversion disorder Ganser syndrome · Somatoform disorder Somatization disorder, Body dysmorphic disorder, Hypochondriasis, Nosophobia, Da Costa's syndrome, Psychalgia · Neurasthenia Physiological/physical behavioral Eating disorder: Anorexia nervosa · Bulimia nervosa Sleep disorder: Dyssomnia Hypersomnia, Insomnia · Parasomnia REM behavior disorder, Night terror · Nightmare Sexual dysfunction: Erectile dysfunction · Premature ejaculation · Vaginismus · Dyspareunia · Hypersexuality · Female sexual arousal disorder Postpartum depression · Postnatal psychosis Adult personality and behavior Personality disorder · Passive-aggressive behavior · Kleptomania · Trichotillomania · Voyeurism · Factitious disorder · Munchausen syndrome · Ego-dystonic sexual orientation · Fetishism Mental retardation Mental retardation Psychological development developmental disorder Specific: speech and language expressive language disorder, aphasia, expressive aphasia, receptive aphasia, Landau-Kleffner syndrome, lisp · Scholastic skills dyslexia, dysgraphia, Gerstmann syndrome · Motor function developmental dyspraxia Pervasive: Autism · Rett syndrome · Asperger syndrome Behavioral and emotional, childhood and adolescence onset ADHD · Conduct disorder · Oppositional defiant disorder · Separation anxiety disorder · Selective mutism · Reactive attachment disorder · Tic disorder · Tourette syndrome · Speech stuttering · cluttering Retrieved from http://en..org/wiki/Creutzfeldt-Jakob_disease Categories: Transmissible spongiform encephalopathiesHidden categories: All articles with statements | Articles with statements since January 2008 | Articles with statements since July 2007 | Articles with statements since August 2008 | Articles with statements since July 2008 | Articles with statements since June 2008 | Articles with statements since June 2007 Views Article Discussion this page History Personal tools Log in / create account Navigation Main page Contents Featured content Current events Random article Search Go Search Interaction Community portal Recent changes Contact Donate to Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Cite this page Languages Català Česky Dansk Deutsch Español Français í•œêµì–´ Hrvatski Bahasa Indonesia Italiano עברית Magyar Nederlands 日本語 ‪Norsk bokmÃ¥l‬ Polski Português РуÑ?Ñ?кий Srpskohrvatski / СрпÑ?кохрватÑ?ки Suomi Svenska ä¸æ–‡ This page was last modified on 29 August 2008, at 16:50
39 Reasons to Drink Acai Juice Every Day
What is MonaVie - Watch the 8-minute video
Discovering MonaVie Video
The Power of You Video
Effects of MonaVie Active on Antioxidant Capacity in Humans
Log into your Wholesale MonaVie Account
So many of us do not eat a balanced diet, get enough sleep, have too much stress, or are impacted with toxins and pollutants. Drinking 2 ounces of MonaVie twice a day will help your body detoxify as well as build your immune system. Its the smartest thing you can do for yourself, so start today. Buying MonaVie through our company guarantees you support 7 days a week and, if you would like to share MonaVie with your family and friends we will guide you from start to finish.
1. Click on Enroll Now (30 - 55% off retail price)
2. Pay $39 for your Wholesale ID number.
3. NO minimum order required.
4. MonaVie is delivered to your door in 3 to 5 days.