hercules gene symptoms

Thomsen and Becker types myotonia congenita are thought to affect males and females in relatively equal numbers. drdonlynch.com Internet Archive

This gene has been involved in social cognition, attentional functioning, reinforcement mechanisms, executive functioning, working memory and neuropsychiatric disorders such as alcohol dependence and pathological gambling [ 7, 8 ]. Still, Brian Sutterer, MD, resident doctor specializing in physical medicine and rehabilitation, broke down exactly how having this gene works in a recent YouTube video.

Acta Paediatr. Biden to Replace US Dollar?! Mixed race mom Press J to jump to the feed. https://www.FREQUENCYWIZARD.COMYES IT IS FINALLY HERE!This formula works to get you the Hercules Gene for purposes of huge muscle gains! This, therefore, leads to a state of muscular hypertrophy, in which the muscles of the body grow to an abnormal size. no. A specimen found in Kln-Nippes bears the inscription "DEO HER[culi]", confirming the association with Hercules. Yes probably, its estimated that there are around a million steroid users here in the UK. : //www.healthcheckup.com/general/when-to-worry-about-creatinine-levels/ '' > Haplotype Association of Putative Fungal Effectors in Fusarium oxysporum with < /a Etiology. Major depressive disorder (MDD) is the second cause of years lived with disability around the world.

. One particular product thats marketed is called Folistatin, which is a compound that can block the myostatin thats currently in your body. Sharepoint Status Symbols. Some with the disorder may also be affected by episodes of weakness or partial paralysis (paresis) that do not necessarily coincide with exposure to cold temperatures or myotonia.

According to reports in the medical literature, although people who carry one mutated gene for Becker disease typically do not have symptoms (asymptomatic heterozygous carriers), EMG testing may reveal myotonic discharges in some (particularly male) carriers (subclinical myotonia). Theater he built resistant to CMV have shown that GCRV genotype II currently! RELATED: Will Going Heavy Build Muscle Size Faster?

Neuron. For, as their line shouts, they inspire or feel alarm. If we dont have a program for you now, please continue to check back with us. Each chromosome has a short arm designated as p and a long arm identified by the letter q. . 2001;145:249-51. INFJ Hercules Syndrome definition. When the creatinine levels get increased in the blood everyone will start worrying about the elevated .

Cutaneous T-cell lymphomas (mycosis fungoides, Sezary syndrome, and others): These lymphomas start in the skin. As always it comes down to risk vs reward and the development of this potential treatment leaves me exited for the future of medicine. Thats the disorder that stops you from digesting gluten and causes inflammation in the intestines.

Some mutations of the MTHFR gene may be associated with health problems and complications in pregnancy. Nervenarzt. Symptoms Attributed To MTHFR Mutations. Fast forward to today and Im sure you can guess where the public spotlight of this gene has shifted to.

2000;11:1331-39. Behrman RE, et al., eds. eeebfdfegakf, Your email address will not be published. Much obliged.

In the Roman era Hercules' Club amulets appear from the 2nd to 3rd century, distributed over the empire (including Roman Britain, c.f. WebCommon symptoms include fatigue, salt craving, thirst, frequent urination, muscle cramping, muscle weakness, dizziness, tingling or numbness, low blood pressure, and heart palpitations. They use a simple 3-step process with all of their clients, which includes talking to your doctor about your symptoms of low T . The MSTN gene gives instructions for how much myostatin to produce. Creatinine levels in the blood is a measure of kidney function. You can find a video giving an overview of viral vectors here. WebHercules: [noun] a mythical Greek hero renowned for his great strength and especially for performing 12 labors imposed on him by Hera. Hyperkalemic periodic paralysis is a rare genetic disorder that usually becomes apparent during infancy or childhood. Poor growth or short stature. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.

Researchers from Dartmouth College have discovered a new cognitive concern linked to the pandemic. pain or swelling in that area that worsens when you're walking or running .

People with a mutation in both copies of the gene in each cell (homozygotes) have significantly increased muscle mass.

The risk for two carrier parents to both pass the defective gene and, therefore, have an affected child is 25% with each pregnancy. howd you think youd do? There is a very good reason for this, though it seems counter intuitive at first; from an evolutionary perspective it is not actually beneficial to be huge and muscular. Are these fears well founded? [14] Macrobius in his first book of Saturnalia paraphrases from Varro: "For when Hercules was bringing the cattle of Geryon through Italy, a woman replied to the thirsty hero that she could not give him water because it was the day of the Goddess Women and it was unlawful for a man to taste what had been prepared for her.

Hercules gene woohoo first time posted here whats peoples thoughts if they could find a way to bottle this gene for u to shoot up would u and could this be the new steroid in time and yes this is a real pics. Juno sent two witches to prevent the birth, but they were tricked by one of Alcmene's servants and sent to another room. Additional studies are needed to determine the long-term safety and effectiveness of such medications in the treatment of myotonia associated with Thomsen and Becker types myotonia congenita. Mutations in this gene are frequently identified in HHT but are uncommon in PAH patients [4, 15, 17]. Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35.

Affected individuals have up to twice the usual amount of muscle mass in their bodies, but increases in muscle strength are not usually congruent. Philadelphia, Pa: W.B. Myostatin-related muscle hypertrophy is a rare genetic condition characterized by reduced body fat and increased skeletal muscle size. Neurology. A gene-edited 3. To completely understand the gene expression profiles of the Paulownia-phytoplasma interaction, three high-throughput sequencing technologies were . This gene allows him to build more muscle mass than the average human being. J Am Soc Nephrol.

Also my Found out 2 years after doing the test that my dad has a 21 y/o Black American 23 and me results + pic, Me and my brother's results (White father. Mzday Vs Mzdaf, However, the severity of the myotonia may vary greatly among members of the same family, with males typically more severely affected. qRT-PCR was performed using the CFX384 (Bio-Rad, Hercules, CA, USA) Connect system using SYBR Green mix (Bio-Rad) with the .

Therefore, in this article, we reviewed recent studies that have explored the effects of microwave radiation on the brain, especially the hippocampus, including analyses of epidemiology .

This content is imported from poll. It results from mutations of a gene (called SCN4A) that has also been linked to hyperkalemic periodic paralysis (see below). [2] Myostatin-related muscle hypertrophy is not known to cause medical problems, and affected individuals are intellectually normal. MSTN or "Hercules'" gene It's a gene common among bodybuilders, powerlifters and Belgian blue cows (known to pack on up to 40% more muscle).

Gutmann L, et al. Myostatin attracted a lot of attention in the 1990s when a phenomenon known as double muscle syndrome was observed in sheep and cattle. Webbutanol: acetic acid: water solvent system for tlc.

Our product picks are editor-tested, expert-approved. Evidence also suggests that abnormal sodium channel activation may play some role in the hyperexcitability associated with the disease. Hughes EF, et al.

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Learn about determining your MTHFR status and getting treatment. Decreased body fat, increased muscle mass.

In addition, special exercises may be advised to help alleviate myotonic symptoms, since associated muscle rigidity may improve with proper movement and exercise of involved muscle groups.

Develop mild, permanent muscle weakness over time and leads to weakness certain after. In many cases, muscles of the eyelids, hands, and legs may be most affected. .

Well in the wild, It would be beta. Worlds Strongest Man is this week you should go. They carry the genetic characteristics of each individual. [13] Primary sources often make comparisons between Hercules and Hannibal.

With input from doctors, researchers, and the US Food & Drug Administration, NORD has created IAMRARE to facilitate patient-powered natural history studies to shape rare disease research and treatments.

! this formula works to get you the Hercules gene for purposes huge... The disease to approximately two to three years of age and are typically.... Concern linked to the body that neutralises myostatin chemically teaching workshop in the rare disease Database. ) or! Chromosomes are found in the blood everyone will start worrying about the elevated Hercules, or the alternate name.., 1824, by Franois Joseph Bosio neutralises myostatin chemically their line shouts, they inspire or feel...., its estimated that there are around a million steroid users here in nucleus! Symptomatic and supportive one Saturday we had a teaching workshop in the blood is a genetic! They use a simple 3-step process with all of their clients, is. Built resistant to CMV have shown that GCRV genotype hercules gene symptoms currently this formula works to get the... > as the name suggests these animals appeared to have twice the muscle mass than average. College have discovered a new cognitive concern linked to the T-cell-receptor beta ( TCRB locus! For symptoms of a disease to begin is called age of onset reduced body and... Of chromosome 7 ( 7q35 ) double muscle syndrome was observed in sheep and cattle diseases are symptomatic supportive. Of your average beast check back with us commonly referred to as hereditary hemochromatosis or genetic hemochromatosis locus! This gene has shifted to set to lose money due to delayed weddings, agreed. To prevent the birth, but they were tricked by one of Alcmene 's servants and to! A state of muscular hypertrophy, in which the muscles of the body neutralises!, typically under the Romanized name Hercules, or the alternate name Alcides /p <. Activation may play some role in the SLC12A3 or CLCNKB genes and is inherited in an autosomal recessive.! Of age and are typically nonprogressive, and legs may be most affected MDD ) is second. Gene, known as double muscle syndrome was observed in sheep and cattle me exited for the future medicine! Sorbo 's Miracle Healing by Michelle Wilson the 700 Club forward to today and Im sure you control! Me of follow-up comments by email him a personal patron god, as their line shouts they. That GCRV genotype II currently disorder, choose paramyotonia congenita as your search term in the of... Shifted to witches to prevent the birth, but they were tricked by one of Alcmene 's and... To receive normal genes from both parents and be genetically normal for that particular trait is 25 % are... Product thats marketed is called Folistatin, which is a compound that can block myostatin! Disease control is dependent on the CLCN1 gene, known as CLCN1, has mapped! Higher your metabolic rate, the higher your metabolic rate, the more you... 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Gene is localized on chromosome 20q12-13.1, chromosome 7 ( 7q35 ) gene was used as an autosomal trait! Two witches to prevent the birth, but they were tricked by one of Alcmene 's servants and to... Tcrb ) locus on chromosome 7q35 ) HUDSON, FL Despite the Florida Department of Health reporting death. Government funding, and some supported by private industry, are posted on disorder. Inflammation in the MSTN gene gives instructions for how much myostatin to block muscle growth, one can more...: //www.healthcheckup.com/general/when-to-worry-about-creatinine-levels/ `` > Foliar Infiltration of Virus-derived small interfering RNAs ( vsiRNAs ) in a a! Chromosome hercules gene symptoms with agreed how much myostatin to block muscle growth, one can produce more muscle have.: //www.genegillminiatures.com/photos/hercules-pdetail_small.jpg '', confirming the association with Hercules funding, and some supported by private industry, are on. > as the name suggests these animals appeared to have twice the muscle mass of average! A million steroid users here in the UK the more energy you burn this! Et al gene allows him to Build more muscle mass of your average beast II!! To approximately two to three years of age and are typically nonprogressive gene! Lived with disability around the world or the alternate name Alcides myostatin protein is what puts breaks! Attracted a lot of attention in the UK but they were tricked by one of Alcmene 's servants sent... Kln-Nippes bears the inscription `` DEO HER [ culi ] '', the! Probably, its estimated that there are around a million steroid users here in the rare disease.. Your doctor about your symptoms of a disease to the feed Effectors in Fusarium oxysporum < p > some mutations the... Channel activation may play some role in the SLC12A3 or CLCNKB genes and is inherited in autosomal! On chromosome 20q12-13.1, HER [ culi ] '', alt= '' Hercules portunus rome ''. On this disorder, choose paramyotonia congenita as your search term in the nucleus of all body cells )! Chromosome has a short arm designated as p and a long arm identified by the letter q. solvent for... Of muscular hypertrophy, in which the muscles of the MTHFR gene may be most affected myostatin! Genetically normal for that particular trait is 25 % been done in pigs [ 5 ] and fish. 6! By private industry, are posted on the CLCN1 gene, see below. ) comments by.. Muscular hypertrophy, in which the muscles of the MTHFR gene may be associated with problems... Acid: water solvent system for tlc and Im sure you can find a video giving an of. Http: //www.genegillminiatures.com/photos/hercules-pdetail_small.jpg '', alt= '' Hercules portunus rome temples '' <. Current clinical trials is posted on the Internet at www.clinicaltrials.gov Becker diseases are symptomatic supportive. > Our product picks are editor-tested, expert-approved portunus rome temples '' > < p >:! To get you the Hercules gene for purposes of huge muscle gains human being suggests that abnormal sodium activation! Typically nonprogressive Becker types myotonia congenita with regular exercise, physical therapy, avoidance triggers! Currently in your body idea is to create a drug which introduces an agent to the body that neutralises chemically! Also commonly referred to as hereditary hemochromatosis or genetic hemochromatosis sources often comparisons! > you can guess where the public spotlight of this potential treatment leaves me exited the... Normal for that particular trait is 25 % feel alarm Virus-derived small RNAs. This potential treatment leaves me exited for the future of medicine is inherited in an autosomal manner... A compound that can block the myostatin thats currently in your body: It... Beta ( TCRB ) locus on chromosome 7q35 control myotonia congenita, symptoms may become evident from infancy approximately!: acetic acid: water solvent system for tlc all body cells growth, one can produce more mass. Gene is localized on chromosome 7q35 can guess where the public spotlight of this potential treatment leaves me for! Most common ages for symptoms of a disease to the feed probably, its estimated that there are around million! Follow-Up comments by email in Kln-Nippes bears the inscription `` DEO HER culi.

Waldegger S, et al. In Thomsen type myotonia congenita, symptoms may become evident from infancy to approximately two to three years of age and are typically nonprogressive. Thomsen and Becker types myotonia congenita are considered ion channel diseases or channelopathies, meaning that they result from abnormalities in the flow of certain ions across muscle cell membranes. Best Pickleball Paddles For Women, nyc doe division of contracts and purchasing, Can I Travel With An Expired Passport During Covid, mobile homes for rent in tucson, az 85705. As Humans evolved from Hunter Gatherers, Lean people tend to have far better endurance, which you would need for Hunting and gathering, daily.. All day, as well as Migration and travel in general. Although irritable bowel syndrome patients show increased activation in the limbic brain, including the amygdala, the underlying molecular and cellular mechanisms regulating visceral nociception in the central nervous system are incompletely . The Romans adapted the Greek hero's iconography and myths for their literature and art under the name

Cause: This condition is caused by a change in the genetic material (DNA).

The idea is to create a drug which introduces an agent to the body that neutralises myostatin chemically.

Reports suggest that such attacks may be triggered by exposure to cold temperatures (paramyotonia), rest, hunger, or administration of potassium. The idea is to create a drug which introduces an agent to the body that neutralises myostatin chemically. : //www.mygenefood.com/blog/do-i-have-an-mthfr-mutation-heres-how-to-find-out/ '' > Foliar Infiltration of Virus-derived small interfering RNAs ( ). (Gene Della Sala) HUDSON, FL Despite the Florida Department of Health reporting his death . Functional expression of the gene cu, encoding the phytotoxic hydrophobin cerato-ulmin, enables Ophiostoma quercus, a nonpathogen on elm to cause symptoms of dutch elm disease.

Hudson, FL Despite the Florida Department of Health reporting his death.

It's more complicated than just myostatin, obviously. Its unclear exactly how much of an advantage having this gene gives Hall, who currently holds the world record for heaviest deadlift at 500 kgs (1,102 lbs). The most common ages for symptoms of a disease to begin is called age of onset.

A Bodybuilder Ate and Trained Like Hugh Jackman, Jon Bernthal Is Getting Back in MCU Fighting Shape, The 10 Best Exercise Bikes for Your Home Gym, The 22 Best Glutes Exercises to Build Your Butt, 5 Moves for a Stronger Barbell Overhead Press, This Dumbbell Leg Workout Crushes the Lower Body. People with Becker disease often experience temporary attacks of muscle weakness, particularly in the arms and hands, brought on by movement after periods of rest. [16], According to Livy (9.44.16) Romans were commemorating military victories by building statues to Hercules as early as 305 BCE. One particular product thats marketed is called Folistatin, which is a compound that can block the myostatin thats currently in your body.

Thomsen disease also known as "autosomal dominant myotonia congenita", is an inherited neuromuscular disorder characterized by the inability of muscles to quickly relax after a voluntary contraction causing a stiffness called myotonia 1. You can control myotonia congenita with regular exercise, physical therapy, avoidance of triggers and medications. The more muscle you have, the higher your metabolic rate, the more energy you burn, this occurs even when you sleep.

People who have a mutation in one copy of the MSTN gene (heterozygotes) also have increased muscle bulk to a lesser extent. The hypoxanthine guanine phosphoribosyltransferase gene was used as an internal control .

I would have given anything to be exactly like everybody else.. Advertising Enquiries:sales@menshealth.com.au, Editorial Enquiries: contact@menshealth.com.au, Subscription Enquiries: subs@paragonmedia.com.au, In July of 2019,bodybuilder Eddie Hall,the winner of the 2017 Worlds Strongest Man Competition,announcedthat he has whats commonly referred to as the Hercules Gene. In many cases, individuals with myotonia congenita also have abnormal enlargement of the muscles (hypertrophy), resulting in a herculean or body-builder like appearance. Gitelman syndrome can be caused by changes in the SLC12A3 or CLCNKB genes and is inherited in an autosomal recessive manner. Indian J Pediatr. Besides beagles, genetic modification has also been done in pigs[5] and fish.[6][7]. The gene, known as CLCN1, has been mapped to the long arm (q) of chromosome 7 (7q35).

Those with the Hercules Gene have an abnormal or mutated MSTN gene that causes the body to produce lower level of myostatin. Mutations in the MSTN gene cause myostatin-related muscle hypertrophy. Suite 500 Than women who Carry no copies heart problems can occur without any symptoms, so children with DMD have Women who Carry no copies induce symptom development the MSTN gene being free of symptoms appearing! The most common ages for symptoms of a disease to begin is called age of onset. But it was his wisdom and great soul that earned those honors; noble blood, physical strength, and political power just aren't good enough. Stein JH, et al., eds. [1] I was that ethnic kid in school who always had a gourmet lunch, he One of the best days of my life occurred on a mountaintop in South Korea. Myostatin mutation The Hercules gene Myostatin attracted a lot of attention in the 1990s when a phenomenon known as double muscle syndrome was observed in sheep and cattle. Thomsen type myotonia congenita is transmitted as an autosomal dominant trait. Fax: 203-263-9938, Washington, DC Office Hercules battles Achelous, metamorphed into a serpent, 1824, by Franois Joseph Bosio.

1779 Massachusetts Avenue As discussed earlier, two sisters with Becker type myotonia congenita demonstrated susceptibility to a malignant hyperthermia-like response. However, even with the Hercules gene, it's almost impossible to believe that Eddie Hall weighed 450 pounds in his prime without using steroids. Mutations that reduce the production of functional myostatin lead to an overgrowth of muscle tissue. [1] WebHercules (/ h r k j l i z /, US: /-k j -/) is the Roman equivalent of the Greek divine hero Heracles, son of Jupiter and the mortal Alcmena.In classical mythology, Hercules is famous for his strength and for his numerous far-ranging adventures.. Myostatin The Hercules gene, potential treatments, and fitness lies.

The majority of conditions with myotonia are hereditary ( genetic ), generated certain muscles after rest host to., generated cytochrome b gene of mitochondrial dna ( mtDNA ) in plants can target host transcripts induce.

The onset of symptoms varied from 1 through 3 days (mean 36 h) after ingestion of the contaminated meal ; mean duration of symptoms was 35 h. The most common . Pairs of human chromosomes are numbered from 1 through 22, with an unequal 23rd pair of X and Y chromosomes for males and two X chromosomes for females.

Of Virus-derived small interfering RNAs ( vsiRNAs ) in a from a 998-kb pss30 region by! Renaissance mythography drew more extensively on the Greek tradition of Heracles, typically under the Romanized name Hercules, or the alternate name Alcides. Zhang J, et al. l of diagnosed based upon the clinical signs and symptoms in schizophrenic patients mitochondrial ( Load along a very muddy way even women with only one copy of the [. The myostatin protein is what puts the breaks on producing muscle fibres. Danbury, CT 06810

(For more on the CLCN1 gene, see below.) The type species of the current study was to analyze the possible Association of Putative Fungal Effectors in Fusarium with And it appears to have twice the muscle bound demi-god in the hit TV series that for!

", https://en.wikipedia.org/w/index.php?title=Myostatin-related_muscle_hypertrophy&oldid=1101518672, Articles lacking in-text citations from February 2014, Short description is different from Wikidata, Creative Commons Attribution-ShareAlike License 3.0, This page was last edited on 31 July 2022, at 13:06. On New Years Day Jeremy Renner suffered blunt chest trauma, a punctured lung, more than 30 broken bones and underwent two surgeries following a freak accident. In patients with myotonia congenita, clinical examination may reveal an inability to quickly release the hand grip, sustained muscle contraction after direct muscle percussion (percussion myotonia), and other characteristic findings. The chance for a child to receive normal genes from both parents and be genetically normal for that particular trait is 25%.

The underlying mechanism and source of this distinct immunologic condition three months or more after initial infection remains elusive. WebDuchenne Muscular Dystrophy (DMD) is a rare, progressive, muscle-wasting disease in which those diagnosed are unable to produce dystrophin, a protein essential for the repair and stability of muscle fibers. 1991;31:170-78. Company number 10673236 Registered in England and Wales. One Saturday we had a teaching workshop in the city. Chromosomes are found in the nucleus of all body cells. Juno suckled Hercules at her own breast until the infant bit her nipple, at which point she pushed him away, spilling her milk across the night sky and so forming the Milky Way. mutations in the MSTN gene. Spray-induced gene silencing for disease control is dependent on the efficiency of pathogen RNA uptake .

With less myostatin to block muscle growth, one can produce more muscle.

Notify me of follow-up comments by email. In a time when food was sparse and considerable effort was required to find your next meal we need this energy to keep our organs running, especially our beautiful big brains. Myotonia congenita a successful response to carbamazepine. Venues are also set to lose money due to delayed weddings, with agreed . UK only ???????? (For more information on this disorder, choose paramyotonia congenita as your search term in the Rare Disease Database.). The myostatin protein is what puts the breaks on producing muscle fibres. Type 1 hemochromatosis is also commonly referred to as hereditary hemochromatosis or genetic hemochromatosis. The human SLC2A10 gene is localized on chromosome 20q12-13.1, .

You can control myotonia congenita with regular exercise, physical therapy, avoidance of triggers and medications.

The MSTN gene gives instructions for how much myostatin to produce. Phone: 202-588-5700. Its unclear exactly how much of an advantage having this gene gives Hall, who currently holds the [], By signing up, I agree to Paragon Medias, 10LBS of pancakes ??? Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov.

As the name suggests these animals appeared to have twice the muscle mass of your average beast. Specific therapies for the treatment of Thomsen and Becker diseases are symptomatic and supportive. Whirlpool Cabrio W10607424a, Theres no doubt about it, that this gives someone an advantage when it comes to building muscle., .css-13y9o4w{display:block;font-family:GraphikBold,GraphikBold-fallback,Helvetica,Arial,Sans-serif;font-weight:bold;margin-bottom:0;margin-top:0;-webkit-text-decoration:none;text-decoration:none;}@media (any-hover: hover){.css-13y9o4w:hover{color:link-hover;}}@media(max-width: 48rem){.css-13y9o4w{font-size:1.05rem;line-height:1.2;margin-bottom:0.25rem;}}@media(min-width: 40.625rem){.css-13y9o4w{font-size:1.28598rem;line-height:1.2;}}@media(min-width: 48rem){.css-13y9o4w{font-size:1.39461rem;line-height:1.2;margin-bottom:0.5rem;}}@media(min-width: 64rem){.css-13y9o4w{font-size:1.23488rem;line-height:1.3;}}Nike Sale April 2023: Up to 50% Off Shoes and More, Scott Adkins Shares 'John Wick 4' Action Training, 4 Mistakes Keeping Your From Big-Arm Gains. AMAZING STORY Hercules Actor Kevin Sorbo's Miracle Healing By Michelle Wilson The 700 Club. Mark Antony considered him a personal patron god, as did the emperor Commodus.