“Caught in the throes of a revolution, I found myself at the Spanish port of Valencia after a tedious 16 hour train journey. After six days and nights a tramp steamer put in, and I succeeded in getting taken aboard to enjoy (sic) the pleasures of a cruise to Liverpool.
I wish the boat wouldn’t roll so much! Down she goes, now she is up again. Still I do not think the rolling is as bad as yesterday, so I will get up and try the Spanish breakfast.
“Buenos Dias” Captain,
“How are you this morning?”
“Oh! Not so bad. I feel I can eat a little to-day”.
“Si, it is nice now”.
The table is set, with places for the captain, first and second mates, and myself. There are two decanters of Spanish wine, a plate of rolls in the centre, and ranged around these are several small dishes. At each place there is a knife, fork, and soup spoon (the same knife and fork is used for all the courses), and four plates, one being for soup.
The “entremeses” or entrée this morning consists of sardinas (sardines), anchoe (anchovy), and hamon (raw ham). Having tasted a little of each, we really started the meal.
EGGS IN OIL
The second course is “Sopa de ajo” in a large earthenware dish, and all that meets the eye at first is about a dozen-and-a-half eggs joined together and lightly fried. Having taken three or four eggs you find underneath a coloured liquid, which is oil, and pieces of bread and garlic. You put this on your soup plate, mix it up, and eat it with your soup spoon. (The boat seems to be rolling more now that I have tasted this dish).
And now for “Bacalao,” or Swordfish, follows. This is served in another earthenware dish with oil or sauce. You eat the fish with bread and wash it down with wine.
While the captain and the others are eating this I take a course in Auto-suggestion, and I find the boat must be now in a calm spot, she is so quiet.
Here is something I can try to eat, it is named “Abichuela con Verza.” This is really a very simple dish, although the name is long, and the recipe is: baked beans decorated with large slices of fat.
NOT IRISH PORK
We are slowly coming to the end, as I find I have only one plate left in front of me. At last something I will feel at home with, “Patatas y Cerdo” (chips and pork). But I am afraid there is something wrong, because it is definitely not the same as Irish pork – still, I can get my teeth into it.
“Yes! I will have some Membrillo” (this is a type of solidified jam, and it is cut into small pieces, and placed – not spread – on the dry bread).
To conclude this early morning feast we will have some black coffee, and a Spanish cigarette, which must be tasted to be known – and will be known at a range of 20 yards ever afterwards.
It is now 10.45a.m., an hour and three-quarters since we sat down, so I’ll finish my cigarette in the air.
TWO MEALS A DAY
I am glad I was able to eat some breakfast because the next meal is timed for 4 o’clock in the afternoon. It is an “old Spanish custom” that you only get two meals per day when at sea. When I eat again, if I am able to, I shall spend about two hours at the table, for at the later meal there will be two other dishes in addition to those I have mentioned.
This article appeared in the newspaper the Irish Weekly Independent on November 24th, 1934. It was written by my father Liam O’Reilly who was 21 years old at the time of writing.
Travelling in the Basque region of northern Spain my father Liam O’Reilly became caught up in the turmoil that was the Asturian miners’ strike of October 1934, an armed uprising by miners and other workers in the mining towns of Asturia in north west Spain, known as the Revolution of Asturias, which developed into the class and regional conflict that became the Spanish Civil War two years later.
In response to a call by opposition anarchists and communists opposing the rising power of the catholic and right-wing Confederation of the Autonomous Right (CEDA) party, on October 4th the armed Asturian miners occupied several towns, while the provincial capital Oviedo was taken by October 6th.
The revolt was finally crushed on October 19th by hitherto unknown General Francisco Franco y Bahamonde. 3,000 miners were killed in the fighting and another 30,000 taken prisoner. Convinced the revolutionary uprising had been meticulously planned by Moscow, General Franco felt the brutal use of colonial Morrocan regulares and the Spanish Foreign Legion troops from Morocco, and the Spanish Navy to repress the revolt (including the torture, rape, and summary execution of Spanish civilians) was wholly justified.
Comparable to my own experience in Beijing in June 1989 (read more at http://wp.me/p15Yzr-r), it is easy to imagine the turmoil, fueled by the Spanish Navy’s bombardment of the Asturian port of Gijon, rumours and counter rumours of port blockades, frontier closures, troop movements, and escalating general strikes which would have caused my father to take flight for the eastern port of Valencia: His Tiananmen Square moment.
My modern day equivalent of a Spanish Tramp Steamer was a Cathay Pacific Boeing 747 from Beijing to Hong Kong (to evacuate about 10 members of the Irish community in Beijing). Unfortunately I don’t recall the menu!
Related reading: ‘4.15pm May 8th 1973’ http://wp.me/p15Yzr-y recalls the day my father Liam O’Reilly went to meet his maker.
Ballyhanna Man – Early Evidence of Hereditary Multiple Exostoses
He occupies pride of place in a specially constructed case at Donegal Museum in Letterkenny, in far-flung rugged North West Ireland, and was a key focus of the Ballyhanna Research Project funded by Ireland’s National Roads Authority (NRA) and involving cross-border collaboration between Queen’s University Belfast and the Institute of Technology in Sligo.
Dating at least 600 years, from 1100-1400, ‘Ballyhanna Man’ was one of 1,200 skeletal remains found by archaeologists around a buried church less than a mile south of Ballyshannon, on the banks of the River Erne, in 2006.
And what makes him so interesting is that he is the first intact case of Hereditary Multiple Exostoses (HME) / Diaphyseal Aclasis to have emerged in Irish archaeology and one of the very few in the world.
Research (which is ongoing) evidence so far indicates he was about a young adult of about 25 years old when he died (typical of the mortality rate of the other non-HME male remains excavated at the burial site). Projecting bony lumps were evident on the upper and lower limbs: Two bones on each lower leg were fused together, and he was knock kneed. His arms were bow-shaped, with the left arm noticeably shorter.
Ballyhanna Man’s condition would have meant he suffered from pain and was very much disabled, and it’s unlikely he would have survived to such an age without some form of support. He appears to have been afforded the same Christian burial as other remains. Regarding his quality of life, given he would have had HME since childhood, who knows?
Given the congenital nature of HME, osteoarchaeologists are working to establish family ties between Ballyhanna Man among the other remains. The remains of a second, man, young to middle aged adult in his late 30’s to 40’s, exhibiting lumps that would have been less obvious than those which afflicted Ballyhanna Man, were also excavated in the same burial ground. According to researchers radiocarbon dating indicates he died several hundred years before Ballyhanna Man, which may point to the HME gene existing within the group for a considerable period of time.
The hope is that in future advancements in genetics and DNA research will provide evidence regarding how HME has evolved.
In addition to the two skeletal remains uncovered by archaeologists at Ballyhanna, two skeletal remains with indications of HME were uncovered by archaeologists in Dublin: The remains of a young to middle-aged female were excavated from a medieval cemetery on St. Stephen’s Street, while a young adult male, dating back to later early Christian era, was exhumed in Kilshane.
In the study of ancient diseases that is paleopathology four of the 16 known cases of HME are specific to Ireland, and a further three cases specific to England (the remaining nine ancient cases of HME are located in Jordan, Zimbabwe, Peru, Sweden, Poland and Canada). As such, is living on an isolated island in any way significant in the context of a higher HME prevalence in the UK and Ireland?
The purpose of this composition (updated March, 2019) is to provide a focal point of support and information for family members and persons living in Ireland and beyond who have Hereditary Multiple Exostoses (HME) in order to encourage them to share their experiences so that people in general will have a clearer understanding of this rare condition and how challenging affected lives can be.
What are the chances of transmitting HME to your children?
Pre-Implantation Genetic Diagnosis (PGD): Karyomapping and MALBAC
Traditional Chinese Medicine (TCM)
Omega-3 Krill Oil
Prognosis – The Good News
HME in Ireland
HME and Autism / Asperger Syndrome linkage?
HME and animals?
Dorsal Foot Exostosis
Is that a bunion or exostosis protruding from your foot?
Orthopaedic / Neurological Consultant / Surgeon HME Know-how in Ireland
Support resources for HME patients and their families
HME and Me
I recall being about nine years old, maybe younger, when I first noticed the large tender lump protruding from my left shoulder blade like a Rhino horn. I soon became very self-conscious as bone protrusions multiplied to cover my legs (femur, tibia, and fibula), arms (humerus, radius, and ulna), shoulder blades, hands, feet, ribs, and pelvis, particularly around the shoulder, elbow, wrist, knee, and ankle joints. My height was affected, as was the shape of my arms (bow-shaped, my left arm is shorter than my right) and legs (my knees won’t bend all the way), with structural impairment to my left elbow and hand. I knew I was different to all my other friends, and with such low self-esteem I certainly felt that way. I hated going to school. I just wanted to seclude myself. As a consequence I was shy and introverted as a child. I wore long sleeve shirts and explained away the bow-like curvature of my left arm by faking how it had been broken. I loved sports, but was unable to participate like other kids my age, while almost nobody, except my mother, knew of the constant 24*7*365 daily pain, the cause of which medical practitioners in the 1970s and 1980s were at a loss to deduce.
The surgery started in earnest when I was 13 years old and by the time I was 27 years old 48 of the more irritating lumps had been hacked, sawed, and chiseled off. The leading orthopedic surgeons in Ireland at the time Messrs. Gerry “Gold Fingers” Brady, John Varian, and Jimmy Sheehan all had a go on me in both Saint Michael’s Private Hospital, in Dun Laoghaire, and the Mount Carmel Hospital, over in Churchtown (Dublin), while I have been also referred to orthopedic consultants, ENT consultants, neurologists (medical interns in tow) and Traditional Chinese Medicine (TCM) practitioners in Liverpool (UK), Seoul (Korea), Singapore, Malaysia, Hong Kong and mainland China.
In 1990, following an operation to remove a lump from my pelvis, I recall the surgeon’s reassuring words “That’s it, no more operations, the bony lumps wouldn’t grow again“, and that I could now get on with my life. I was 27 years old and I’d gone through more operations, physiotherapy, and recovery periods and overcome more obstacles than anyone should ever have to go through in their entire life. So get on with my life I certainly tried to do, and did.
However, despite leading as active a life as I could, the ever present twinge, spasm, ache, and clicking sound, which I guess only a person with HME can truly identify with, continued and in 2008 I was referred to neurologist Mr. Chris Pidgeon at Dublin‘s Beaumount Hospital. He advised surgery on compressed cervical vertabra caused by atypical spinal curvature on the basis that if I didn’t have such surgery sooner rather than laternerve damage and dysfunction would gradually lead to acute lack of sensation on the left side of my body. At around the same time one of China‘s leading ENT experts, Professor Pu Xing Kuan (JiangSu Province Hospital, Department of Oto-Rhino-Laryngology -卜行宽, 江苏省人民医院耳鼻咽喉科卜行宽主任医师) postulated a connection between the bony growths and troubling hearing and balance challenges.
New medical knowledge gleaned through advances in scientific research indicate that intermittent fatigue, poor coordination and short concentration span troubles I have always tried to come to grips with are neurological motor disorder symptoms associated with HME, and not just a figment of my imagination.
By and large living with HME has been a largely silent battle marked by good and bad days. While the bad days don’t define me, they do seem to be happening more often than I care to admit. I would describe a good day as a day when things are manageable, when the level of needling pain is at least two levels below my average. Regardless, in spite of the challenges that come with the territory, I will never let HME beat me.
What is Hereditary Multiple Exostoses?
The condition was first alluded to in 1786 by John Hunter, the prominent, yet controversial, Scottish surgeon and anatomist, infamously known for taking possession of 2.31 metres tall Irish giant Charles Byrne’s corpse contrary to Byrne’s clear deathbed request. It would take a further 90 years for the term ‘multiple exostoses’ to first surface, as conceived in 1876 by the venerated German physician Rudolf Virchow. What is more, the first reference to Hereditary Multiple Exostoses (HME) in American medical literature only happened in 1915 when the Boston surgeon Albert Ehrenfried wrote of “Multiple cartilaginous exostoses—hereditary derforming chorodysplasia: A brief report on a little know (sic) disease”.
Hereditary Multiple Exostoses (HME) is one of the numerous synonyms [along with: Bessel-Hagen Syndrome;Chondral Osteogenic Dysplasia of Direction;Chondral Osteoma;Deforming Chondrodysplasia; Diaphyseal Aclasis (multiple hereditary); Dyschondroplasia;Exostosing Disease; Exostotic Dysplasia;Exostosis Multiplex;EXT; Hereditary Deforming Chondrodysplasia;Hereditary Multiple Osteochondromas;Multiple Cartilaginous Exostoses;Multiple Congenital Osteochondromata;Multiple Exostoses;Multiple Hereditary Exostoses (MHE); Multiple Hereditary Osteochondromatosis (MHO); Multiple Osseous Exostoses;Multiple Osteochondromas (MO – which is the term designated by the World Health Organisation (WHO)); Multiple Osteomatoses; Osteochondromatosis; and Osteogenic Disease] is a very rare bone disease in which multiple benign bony cartilage-capped outgrowths (or exostoses /osteochondromas) thatare atypical in size, position and number grow in areas of active bone development, or open growth plates, in children.
Regarding HME’s origins scientists have linked it with chromosomal mutations in three genes: EXT1, which maps to Chromosome 8q24.1; EXT2 which maps to Chromosome 11p13; and EXT3 which maps to the short arm of Chromosome 19 (though its precise location is still unclear). It seems the majority of HME cases have either HME EXT1 or HME EXT2 mutations, while a small proportion of HME cases are linked to the EXT3 gene.
Approximately 50% of people with HME are diagnosed by the time they are three years old
5% of newborns that carry an HME gene show some signs at birth
Though not present at birth, 96% of all cases with HME will show noticeable signs by the time they are 12 years old
Approximately 70% of people with HME have an exostosis or bone abnormality around the knee
Six is the number of exostoses the average person affected with HME will typically develop during his or her life
Most often affected are long tubular bones, while in 10% of cases the small bones of the hands and feet are also affected, the scapula only in 1% of patients. The spine is involved only in 2%, but it can lead to cord compression.
While HME currently has no cure, the good news is that a cure may not be far away!
FANTASTIC NEWS FROM MARCH 2018
Update March 2018: MHE Research Foundation in collaboration with Clementia Pharmaceuticals is has announced recruitment for the trialing in Australia, Belgium, Canada, France, Italy, Japan, Portugal, Spain, The Netherlands, Turkey, United Kingdom and United States ) of (once daily pill) the efficacy and safety ClementiaPalovarotene, as a potential treatment of HME in children.
Research moves toward the first drug treatment for Hereditary Multiple Exostoses
Prevalence and geographical reach
Curiously, the research also points to much higher prevalence rates amongst island populations with geographically restricted movement, such as Guam, which has about 100 HME cases per 100,000 people.
Be that as it may, taking for granted that Ballyhanna Man, and the two age-old skeletal remains discovered in Dublin, proved HME’s existence in Ireland over 600 years ago one would be inclined to think that given its hereditary nature the prevalence of HME among their future ascendants on the island would be relatively high. In actuality, secondary research and interactions with orthopaedic surgeons and online support groups undertaken by myself suggest there may be less than 100 cases on the island of Ireland (April, 2018).
Geographically, while the primary HME clusters are to be found in Europe, North America, and Australia, HME is a global disease with people impaired by the condition living in China, India, South East Asia, South America and Africa.
Chloe B tells the story behind the scars
An exotosis is a benign rounded or sharp bone growth at the metaphyseal areas of the long bones. Exostoses start, and continue, growing, for the duration of a child’s development around the growth centres of bones that are near the ends of the bones, which is why lumps tend to grow, or fuse, near the joints. When a person has achieved full skeletal growth, the exostoses are expected to stop growing, which is not to say their tenderness also stops. This last point is quite contentious, as previously less painful exostoses can become very tender with the wear and tear of age. Moreover, exostoses can also return to the same places from where lumps have been previously extracted, and they may be more painful. Many members of online HME support communities highlight increasingly chronic pain experienced in later life.
What is an Osteochondroma?
Chronic, not contagious
What complications are caused by HME?
HME can be particularly troublesome. Because the exostoses grow around areas of active bone growth, they disrupt the normal growth process, leading to defective growth that causes nerve compression, inequality of limb length and irritation of adjoining soft tissue, such as skin, nerves, tendons, muscles, and blood vessels. Such is their sensitivity, these cartilage-capped lumps can cause chronic pain, clicking sounds, and numbness until they are surgically removed. Accidentally bumping them against something solid can be particularly painful.
Exostoses that grow near the ends of long bones may limit the normal range of motion of the joints upon which they encroach. Consequently, people with HME may have a shorter stature than average, with studies of HME patients showing the final height in men typically averaging 170 cm (66 in), while the average height in women is about 160 cm (62 in). Moreover, differential rates of growth between a child’s legs or arms can result in disparities in leg or arm length sometimes reaching 2 cm (1 in) or more. Leg length disparity can result in hip pain and difficulties with walking caused by a slanting of the pelvis.
HME patients may also have bowed arms or legs. Often, the forearm will bow out, or the legs can grow to be “knock-kneed“. While function is usually fairly normal, the bowing can be very troublesome.
Another complication caused by HME is stiffness, particularly in the hands, elbows and hips usually because the lumps block their natural movement.
The most alarming potential HME complication is also one of the rarest, typically occurring after skeletal growth has finished. In less than 1% of cases the benign exostoses can become a cancerous tumor called Chondrosarcoma. Such Chondrosarcoma cases are usually in the 20’s to 50’s age range. Growth and soreness are two key warning signs that a benign tumor has become malignant. If a person with HME notices after they have stopped growingthat an exostosis is getting larger or painful he or she should consult their doctor right away. Chondrosarcoma while uncommon (arising in0.5% to 3% of HME patients) is still something people who have Hereditary Multiple Exostoses must know about. An unnoticed bone malignancy always presents a risk of metastasis (the spreading of cancerous cells elsewhere in the body), which is one of the most dangerous complications of any cancer (For more on Chondrosarcoma check out this YouTube video explanation from Dr. Christopher R. Beauchamp, M.D., Orthopedic Oncology and Adult Reconstruction Surgery, Mayo Clinic ).
Hereditary Multiple Exostoses (HME) [Multiple Hereditary Exostoses (MHE), Hereditary Multiple Osteochondromas, Multiple Exostoses, Exostosis Multiplex, Multiple Osseous Exostoses, Multiple Cartilaginous Exostoses], or Diaphyseal aclasisis a condition that is passed by the genes of the affected parent to their children. If one parent has the condition, there is a 50% likelihood that any child could also develop Hereditary Multiple Exostoses (HME).
As is my own situation, in 10% to 20% of HME cases a person can develop multiple exostoses with no family history of HME. In medical terms this is referred to as a de novo or “spontaneous mutation” indicating a genetic problem arose in that person without being inherited from a parent. Moreover, my two brothers, who are both in their 60s, did not inherit this condition.
HME has a 96% penetrance, which means that if the disease is indeed transmitted to a child, he or she will have a 96% chance of actually manifesting the disease, and 4% chance of having the disease but never manifesting it.
While males who have the HME gene tend to exhibit more obvious and severe symptoms than females, and are therefore more likely to be diagnosed with HME, males and females are equally likely to inherit HME.
Straight talking exostoses boy Mikey spells it out in black and white
What are the chances of transmitting HME to your children?
A person with HME has a 50% chance of transmitting this condition to his or her children. Male and female are equally likely to be affected. In other words, if it is assumed that four children are produced, and one parent is a carrier and exhibits the disease, the statistical expectation is for two children to be normal and two children to inherit this disease. This does not mean that children will necessarily be affected; it does mean that each child has a 50:50 chance of inheriting the disorder.
Pre-Implantation Genetic Diagnosis: Karyomapping and MALBAC
For individuals with HME who are considering starting a family, recent scientific developments in pre-implantation genetic screening and diagnosis (PGS & PGD) and pre-natal diagnosis can detect the exostoses gene from embryo samples and help select normal embryos. [Note: For further information about PGS refer to the ‘Research’ section below].
In February 2015, confirming the significance of pre-implantation genetic diagnosis with respect to detecting the exostoses gene the Cork Fertility Centre , stated:
“We do provide PGD service for Multiple Exostoses patients based on Karyomapping technic, which can do the same job as MALBAC. Karyomapping can detect the exostoses gene from embryo samples and at the same time obtain the information of chromosome status. ” (Source: Cork Fertility Centre email to author of this blog piece, dated 15th February, 2015).
The Beacon CARE Fertility centre in Sandyford, Dublin, also provides pre-implantation genetic testing services.
FANTASTIC NEWS FROM SEPTEMBER 2014
“Hereditary Multiple Exostoses patients can now expect their offspring to be free from their disorders”
Beijing (Peking) University, Sep.24, 2014: On September 19, 2014, the first in vitro fertilization (IVF) baby with pre-implantation genomic screening based on MALBAC was born in the Beijing University Third Hospital, Beijing, China. MALBAC is a newly developed whole genome amplification method, allowing for the precise selection of embryos in the IVF process when combined with next generation sequencing. This event brings the good news to patients with monogenic diseases around the world that they can now expect their off springs free from their disorders.
In this case, the husband suffers from Hereditary Multiple Exostoses, an autosomal dominant hereditary disorder, which is characterized by multiple bony spurs or lumps on the bones at an early age. There is a frame-shift point mutation at the EXT2 gene of this patient, which has a 50% chance of transmitting this disorder to his children. To avoid this risk, a normal embryo free from the husband’s disease allele was selected by Dr. Jie Qiao’s group at Beijing University Third Hospital using the MALBAC technique that was developed by Sunney Xie’s lab.
Total 18 embryos at blastocyst stage were obtained from the couple during IVF cycle, and a few cells were biopsied from each of the day 5 or day 6 embryo. Genomic DNAs of the obtained cells were amplified evenly and accurately with the MALBAC method for the whole genome sequencing analyses. Combined with the targeted PCR and next generation sequencing techniques, all the numerical and structural chromosome abnormalities and the mutated allele of the genetic disease were accurately detected with low depth sequencing data (0.1X). The team identified three embryos with neither the inherited mutated allele nor chromosome copy number abnormalities from these 18 embryos, and finally chose one healthy embryo to transfer back to the wife. The embryo implanted successfully, grew normally, and later the amniotic fluid cells from the baby were isolated and analyzed as free of aneuploidy and mutated allele. Now the baby was born successfully, with 4.03 kg of weight and 53 cm of length. Umbilical cord blood genome detection confirmed the baby is free of the mutated allele.
Pre-implantation genetic diagnosis (PGD) is a technique that helps selecting normal embryos to transfer into uterine using IVF. It is an early prenatal diagnosis technology to obtain a healthy offspring by avoiding the genetic diseases.
Currently, the widely used PGD technologies are fluorescence in situ hybridization (FISH), polymerase chain reaction (PCR), and comparative genomic hybridization (Array-CGH) and single-nucleotide polymorphism (SNP-array)… it has been highly desirable, but has not yet been reported to simultaneously detect monogenic point mutations and chromosome abnormalities. MALBAC allows for simultaneous circumvention of point mutations and chromosome abnormalities with high accuracy. Furthermore, the procedure developed by the team has used low depth sequencing, allowing low cost and fast PGD.
MALBAC, a powerful single cell whole genome amplification method, which was first developed and reported by Sunney Xie’s lab in 2012, is the key technique in this project. Since MALBAC use linear instead of exponential amplification, it is much more accurate and uniform than the traditional DOP-PCR and MDA methods. So MALBAC can be used to analyze the genomes of rare and limited materials. At the end of 2013, Sunney Xie’s lab cooperated with Jie Qiao’s team and Fuchou Tang’s lab and demonstrated the proof of principle of using MALBAC for PGD in IVF, which was published in Cell.
The project is done with the support from the Ministry of Science and Technology, Beijing Municipal Science and Technology Commission, the National Natural Science Foundation of China, and 985 project of Peking University. The project is accomplished under the cooperation of the three partners: Jie Qiao’s team in Peking University Third Hospital, Sunney Xie’s lab and Fuchou Tang’s lab in Biological dynamic Optical Imaging Center (BIOPIC) of Beijing University.
Ruby Page explains what it’s like to live with HME
Some people with HME never need any treatment. They learn to counterbalance the abnormality or reduced range of motion so they can perform as normally as possible. When abnormality does occur it often develops so slowly that the patient can adjust to it well, while others may require surgical treatment to provide relief.
Surgery (bear in mind modern medicine has really advanced with ongoing technological breakthroughs!), physiotherapy and pain management are currently the only options available to HME patients, and while success varies from patient to patient many continue to struggle with pain, fatigue and mobility problems throughout their lives.
It is not unusual for patients with Hereditary Multiple Exostoses (HME) [Multiple Hereditary Exostoses (MHE), Hereditary Multiple Osteochondromas, Multiple Exostoses, Exostosis Multiplex, Multiple Osseous Exostoses, Osteocartilaginous Exostoses, Multiple Cartilaginous Exostoses], or Diaphyseal aclasis to undergo numerous surgical procedures throughout their lives to remove painful or deforming exostoses, correct limb length discrepancies or improve range of motion.
HME Presentation by Dr. Dror Paley, Paley Limb Lengthening Institute, St. Mary’s Hospital, West Palm Beach, Florida
If an exostoses is painful, pressuring an important structure, visibly unsightly, or is easily knocked, it can be removed by surgical methods. Excision itself is usually a fairly straightforward procedure, some are removed without necessitating an overnight stay in hospital. Once removed, however, as previously mentioned, exostoses can reappear (about 20% – 50% of the time), although they are may not grow to the same extent as before.
When an exostosis causes a growth deformity, such as bowing, sometimes simply cutting off the lumps at an early stage will let the bone straighten itself out and adapt as the child grows. However, some bowing is so acute that not only must the lumps be removed, but also the bone must be straightened. This can be done either by cutting the bone, remodeling it and then holding it in place while it mends or, if the child is still developing, by altering the rate of growth on one side of the growth plate.
There are a number of options available and an orthopedic doctor should be able to advise accordingly.
Moses Ndiritu’s story – Every day gets harder
Managing the severe pain associated with HME can be very disheartening, and there are all sorts of opinions regarding treatment. Below are several different approaches to pain management, notwithstanding that fact that in distinguishing which pain medicine provides the most effective relief it is important for each HME patient (or parent / guardian in the case of children) to do their own research before any new treatments are commenced. While a proposed treatment may sound beneficial, there are also some potential negative side effects that a HME patient may suffer from. Always be aware of both the pros and cons of any treatment before deciding whether it is the right approach to controlling specific pain, and preferably use the therapy in a controlled environment.
1. Medical Marijuana?
While the MHE Research Foundation does not support the use of Medical Marijuana, HME is one of a defined number of conditions with symptoms or ailments that advocates claim can treated with Medical Marijuana. Stockbroker and HME patient Irvin Rosenfeld, from Fort Lauderdale, Florida, has been issued with 12 daily government-supplied marijuana cigarettes for more than 30 years. The longest surviving patient to be assigned to the federal medical marijuana, Mr. Rosenfield claims he would not be alive if he hadn’t been issued with marijuana cigarettes for the treatment of his HME condition.
For more on Irvin Rosenfeld (http://irvinrosenfeld.com/), refer to the YouTube video ‘Medical Marijuana – Multiple Exostoses (Irvin Rosenfeld)’ below.
In Canada, Saskatoon high school student Michael Wileniec says high-grade medical marijuana is the only drug that eases his chronic pain, noting in a January 2015 newspaper interview, he had already “…tried conventional prescription drugs, from Tylenol 3 to morphine, but didn’t like how they clouded his mind“.
For more about Michael Wileniec and his usage of Medical Marijuana to help alleviate HME related pain refer to:
Having lived in China for a number of years I have had the benefit of trying out traditional acupuncture, electroacupuncture, and tuina acupressure, the needle free alternative to acupuncture. These Traditional Chinese Medicine treatments are effective paint controls, although I found the relief to be short lived, meaning that once treatment concluded the soreness would soon return. For specific HME patient feedback regarding the effectiveness of such Traditional Chinese Medicine practices, including qigong read the “Comments” https://nialljoreilly.com/2012/04/28/hereditary-multiple-exostoses-ireland/#comments section located at the bottom of this post.
Learning to Love Myself and My Scars From Multiple Hereditary Exostoses
3. Omega-3 Krill Oil?
Having endured an agonising winter of 2013 / 2014, to the point where even a walk of 20 metres could be a harrowing exercise -the degree of tenderness contingent on the prevailing weather- my introduction to the benefits of Omega-3Krill Oil, which the Journal of Lipid Research claims is 48 times more potent than fish oil, was simply a business-driven fluke. Yet, while there are no research studies to back me up, I have found exceptional relief (reduced pain, inflammation, functional impairment, stiffness) since the summer of 2014 when I started taking Omega-3Krill Oil in capsule (500 mg per day) and more recently in syrup format. In fact, of late, since finishing the bottle of Omega-3Krill Oil (300 ml) syrup in late January (2015), once again I can now feel both bone and joint pain levels starting to give me a hard time.
The Omega-3 Krill Oil capsule and syrup products I used are from CleanMarine (http://www.cleanmarine.ie/), who also produce a Krill Oil syrup for kids.
Advocates of homeopathy for HME contend that surgical excision of exostoses does not remove the cause of HME, as it cannot guarantee further exostoses from forming. Homeopathists aim to treat the patient (not HME) by strengthening his/her immune system to remove the disease and prevent recurrence.
FANTASTIC NEWS FROM NOVEMBER 2017!
“Preclinical study demonstrates promising treatment for rare bone disease
Data supports clinical investigations of palovarotene to treat multiple hereditary exostoses”
La Jolla, Calif., November 20, 2017 – Researchers at Sanford Burnham Prebys Medical Discovery Institute (SBP) have led a preclinical study demonstrating that the drug palovarotene suppresses the formation of bony tumors (osteochondromas) in models of multiple hereditary exostoses (MHE). The research, published in the Journal of Bone and Mineral Research, is an important step toward an effective pharmacological treatment for MHE, a rare genetic condition that affects about 1 in 50,000 people worldwide.
MHE (also known as multiple osteochondromas, or MO) is an inherited genetic disorder in which multiple benign bone tumors covered with cartilage grow at active areas of bone growth. The condition is caused by mutations in two genes: EXT1 and EXT2. Individuals with these mutations develop painful, debilitating tumors, often repeatedly during their childhood and adolescence. Surgery and pain management are currently the only treatment options for MHE patients.
“Our study shows that palovarotene is a remarkably potent inhibitor of osteochondromas, says Yu Yamaguchi, M.D., Ph.D., professor at SBP. “In our mouse model of MHE, we were able to reduce bone tumors by more than 90 percent, which is a significant improvement over the previous drugs we have tested in the same mouse model.”
“Especially promising is that palovarotene has been tested for toxicity and side effects in humans and has been shown to be well tolerated,” says Yamaguchi. “This means that time line for getting the drug to the clinic for MHE may be shortened.”
Clementia Pharmaceuticals licensed palovarotene from Roche Pharmaceuticals, which previously investigated the compound as a possible treatment for chronic pulmonary disease and evaluated its safety in more than 800 healthy volunteers and patients. Clementia Pharmaceuticals is planning to initiate a Phase 2/3 clinical trial in 2018 for patients with MHE.
“This is first time we are seeing a clear path toward a therapy that will improve the lives of MHE patients and their families,” says Sarah Ziegler, vice-president of the MHE Research Foundation. “The long awaited first clinical trial for a drug to treat MHE is now a reality. This breakthrough comes after years of working with medical professionals and scientists like Dr. Yamaguchi to achieve something we have all been desperately striving for, for many years.”
Through gene mapping studies scientists, as previously noted, have linked HME with mutations in three genes: EXT1, which maps to Chromosome 8q24.1; EXT2 which maps to Chromosome 11p13; and EXT3 which maps to the short arm of Chromosome 19 (though its precise location is still unclear).
Continuing research of the HME genes will likely establish an accurate prevalence for each of the three gene types, thus providing greater insight into the growth of cells, which is really what HME is all about. With such rapid advances in science, particularly in terms of gene mapping, it not inconceivable that such as understanding will sooner rather than later provide the knowledge leading to a tangible treatment for HME.
Recently, Chinese scientists, supported by the Ministry of Science and Technology, have also started conducting extensive research into HME. One such research paper published in 2014 concluded that in China:
“HME starts earlier and becomes more severe and extensive with each successive generation in members of the pedigree analyzed”
[For more about HME in China refer to ‘10. Instances of Hereditary Multiple Exostoses (HME) in China, from 1990 – 2013′ in the research segment at the bottom of this blog.
As it stands, gene mapping can serve as a basis for testing children at risk with HME and the information gleaned from such testing will hopefully lead to the prevention of the development of exostoses and their associated complications. There is good reason for optimism: the day when our doctors are equipped to undertake such testing is near.
Multiple Hereditary Osteochondromatosis (MHO)* – Suzie’s Story
*Multiple Hereditary Osteochondromatosis is the official World Health Organisation term for HME / MHE
HME in Ireland
Osteochondroma… this is My story
HME and Autism / Asperger Syndrome Linkage?
Heparan Sulphate and MHE – Dr. Yu Yamaguchi. Many parents of children with MHE / HME / MHO frequently observe autism and Asperger Syndrome like social issues in their children
“….“The bumps themselves are not so much a problem, what tends to cause the issue in children or even in adults is if [the bumps] are causing deformity,” explains Dr. Carmen Brauer, an orthopediatric surgeon with the Alberta Children’s Hospital. “Bone lengthening in the upper extremity is fairly rare compared to the lower extremity, and here at the Alberta Children’s Hospital we hadn’t done any lengthening of the upper extremity,” Dr. Brauer says. A team was assembled to perform the first procedure on Dunbar last June. His bone was cut and a device was implanted to apply tension over time to help the bone to grow. “We slowly distract and the bone then heals under the tension we’re applying. By doing that we can lengthen the bone up to a millimeter a day,” Dr. Brauer explains…….” Source / read more and view the Video: http://globalnews.ca/news/907083/bone-lengthening-surgery-saves-calgary-boy-from-disability/
Dorsal Foot Exostosis
Dorsal foot exostosis is a bony growth on the dorsum (top) of the foot. It can occur where the first metatarsal joint meets the big toe, causing the toe to lose its ability to bend. This is also known as Hallux rigidus (inability to move the joint) or Hallux limitus (limited movement of the big toe). Acute or chronic pain on the top of the foot happens in the morning and as the day progresses, more so the longer a person is standing. Metatarsal Cuneiform Exostoses crop up in the midfoot area, where the first metatarsal shaft meets the cuneiform, while a forefoot version of Haglund’s Deformity is where the throat line of the shoe meeting the foot causes pressure and rubbing which results in the fleshy area behind the toes..
Is that a Bunion or an Exostosis protruding from your foot?
– “A large exostosis was the source of a bunion deformity in a 60-year-old woman. Its unusual clinical and radiographic features were suggestive of a bizarre parosteal osteochondromatous proliferation. However, histologic features were most consistent with a benign osteocartilaginous exostosis…..” Source / read more: http://www.ncbi.nlm.nih.gov/pubmed/11482512
Orthopaedic / Neurological Consultant / Surgeon HME Know-how in Ireland
Unfortunately GPs / HSE in Ireland have little or no knowledge of HME. Best to have a GP refer you to an orthopedic consultant specialising in the specific area that causes most discomfort. No one consultant will cover all areas affected by HME. Below is what I would consider to be the best orthopaedic surgeon team in Ireland. These guys are very well grounded, they know the score and have the know-how when it comes to dealing with HME. Typically, the first consultant you engage with should take the lead in calling in other orthopaedic specialists either to verify a particular prognosis or to advise on specific areas beyond his area of expertise.
Mr. Hannan Mullett (Shoulder), Blackrock Clinic, Beaumont Hospital, Sports Surgery Clinic, Cappagh National Orthopedic Hospital
Mr. Philip P. Grieve (Elbow, Hand, and Wrist), Blackrock Clinic
Mr. Alan Liang (Foot and Ankle), Blackrock Clinic
Mr. Fintan Doyle (Hip and knee), Blackrock Clinic
Mr. Eoin Fenton (Neurosurgery, Spine), Blackrock Clinic
Dr. Sean Connelly (Neurophysiology), Blackrock Clinic
Tip: Make sure you have health insurance. MRIs at Blackrock Clinic should be fully covered by VHI, but not CTs. CTs are fully covered by VHI at the Affidea clinics. For x-rays public hospitals have walk in services, which cost about €50.00, rather than €100.00 + in the private hospitals
Useful Support Resources for HME patients and their families
– This support group offers a German translation of The MHE and Me Handbook
Hereditary Multiple Exostoses (HME) and Mehttp://wp.me/p15Yzr-Mr – Despite evidence of HME occurring in 4 ancient Irish skeletal remains (“Ballyhanna Man“) of only 16 ancient skeletal remains worldwide diagnosed with HME bone growth disorder, Ireland doesn’t have an HME information support group, hence this blog.
National Center for Biotechnology Information (NCBI) http://www.ncbi.nlm.nih.gov/sites/ga?disorder=multiple%20hereditary%20exostoses – Up to date website with detailed information on Hereditary Multiple Exostoses (HME). Includes: * Links to introductory material about Multiple Hereditary Exostoses and genetics. * NCBI Book sections and chapters about Multiple Hereditary Exostoses and genetics. * Recent scientific articles about Multiple Hereditary Exostoses. * Links to resources for screening, genetic testing, and directories of specialists.
PAPER – Cervical spinal cord compression in hereditary multiple exostoses Abstract– Spinal cord compression is an extremely serious complication of hereditary multiple exostoses (HME). A case of HME with compression of the cervical spinal cord is reported. Complete recovery following surgery was achieved. A review of the relevant literature revealed 51 previous cases of HME with cord/cauda equina compression. Most patients were under 30 years of age with more men affected than women. The family history was positive in 60%. The cervical and thoracic areas were predominantly affected, with the symptoms usually developing slowly. Recovery following surgery is to be expected in the majority of cases. In patients with HME and suffering from neurological symptoms, the possibility of spinal cord compression should be considered. Prompt diagnosis and surgical excision provide the best prognosis. Source / read more: http://www.ncbi.nlm.nih.gov/pubmed/9006779
ONGOING RESEARCH – Call for participants – Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary Exostoses: Multicentre Project.
PAPER (Chinese)- Ultrastructural features of hereditary multiple osteochondroma cartilage cap in children Abstract –目的观察儿童遗传性多发性骨软骨瘤（hereditary multiple exostoses, HME）软骨帽的超微结构，为儿童HME超微病理诊断提供可靠依据。方法实验组：切除18例HME患儿肋骨瘤体分离软骨帽；对照组：15例胸廓发育畸形患儿手术矫正切除的肋软骨；分别取其纵、横切面应用扫描电镜和透射电镜观察。结果对照组：冷冻断裂的软骨组织内见少量软骨细胞位于软骨陷窝内，软骨组织表面可见大量散乱、稀疏的胶原纤维；软骨细胞数量不多，细胞表面有少量短小的微绒毛，细胞核形状不规则，细胞质内可见到粗面内质网呈条索样分散在细胞质内，线粒体较小，糖原颗粒呈簇状分布。实验组：冷冻断裂的软骨组织内见大量不规则的软骨陷窝，每个软骨陷窝内均含有软骨细胞，细胞表面有丰富的细胞突起；软骨组织内见大量瘤样细胞增生，聚集分布，细胞核较大，细胞质内可见圆形或椭圆形的线粒体及扩张的粗面内质网；瘤细胞间可见毛细血管，其附近可见明显增多的软骨细胞，软骨细胞体积较对照组增大。结论儿童HME软骨帽的超微结构改变（细胞形态及细胞内部细胞器），不同于正常软骨细胞，可能与儿童HME的遗传、发病、发展、转归因素密切相关。 Source / read more: http://www.cjcep.com/oa/darticle.aspx?type=view&id=201302014
PAPER – Multiple osteochondromas in the archaeological record: a global review Abstract
…The paper undertakes the ﬁrst synthesis study of the 16 known cases of the condition that have been identiﬁed in the international palaeopathological record. It also includes information derived from two newly discovered cases of the disease in two adult male individuals recovered from the Medieval cemetery at Ballyhanna, Co. Donegal, Ireland. Source / read more: http://www.qub.ac.uk/sites/Ballyhanna/FileStore/Filetoupload,216459,en.pdf
7. PAPER – Hereditary Multiple Exostoses: A Current Understanding of Clinical and Genetic Advances…Recent advances in understanding the molecular and genetic basis of this condition not only offer hope for patients and families with HME, but also offer clues to the underlying basis for the formation of the human musculoskeletal system… Source / read more: http://upoj.org/site/files/v14/v14_09.pdf
“In medicine and (clinical) genetics preimplantation genetic diagnosis (PGD or PIGD) (also known as embryo screening) refers to procedures that are performed on embryos prior to implantation, sometimes even on oocytes prior to fertilization. PGD is considered another way to prenatal diagnosis. Its main advantage is that it avoids selective pregnancy termination as the method makes it highly likely that the baby will be free of the disease under consideration. PGD thus is an adjunct to assisted reproductive technology, and requires in vitro fertilization (IVF) [Note: IVF costs around €4,000, with fertility drugs, if required, costing up to €3,000] to obtain oocytes or embryos for evaluation.
PGD is also now being performed in a disease called Hereditary multiple exostoses (MHE / MO / HME)..
The term preimplantation genetic screening (PGS) is used to denote procedures that do not look for a specific disease but use PGD techniques to identify embryos at risk. PGD is a poorly chosen phrase because, in medicine, to “diagnose” means to identify an illness or determine its cause. An oocyte or early-stage embryo has no symptoms of disease. They are not ill. Rather, they may have a genetic condition that could lead to disease. To “screen” means to test for anatomical, physiological, or genetic conditions in the absence of symptoms of disease. So both PGD and PGS should be referred to as types of embryo screening….” Source / read more: http://library.everyonehealthy.com/library/furthertest/In%20Vitro%20Fertilization%20With%20Preimplantation%20Genetic%20Diagnosis
9. NEW RESEARCH: How gene mutations lead to the abnormal bone growth that is Hereditary Multiple Exostoses (MHE)?
In humans, MHE is caused by a mutation in one of two genes, Ext1 or Ext2. Together, these genes encode an enzyme necessary to produce heparan sulfate—a long sugar chain that facilitates cell signals that direct bone cell growth and proliferation. But when these genes were inactivated in mice just as they are in human MHE patients, the mice failed to develop the symptoms of MHE. This had scientists scratching their heads.
Enter Dr. Yamaguchi and his colleagues, who took a different approach. Instead of knocking out the Ext1 gene in the whole mouse, they targeted the gene only in bone cells. Moreover, they deleted the gene in only a small fraction of these cells. Surprisingly, this minimalistic approach led to a mouse with all the physical manifestations of MHE, such as bony protrusions, short stature and other skeletal deformities.
The new mouse model answered some long-standing questions about MHE. Scientists had gone back and forth on whether the abnormal growths observed in MHE are true tumors or just malformations of the bone. In this study, the protrusions were made up of two cell types. A minority were mutant cells lacking Ext1, but, amazingly, most were normal bone cells. True tumors, in the strictest sense, arise from the proliferation of mutant cells only. Hence, MHE bone protrusions must result from a different – though still very serious – type of growth.
“I have been waiting 13 years for this breakthrough,” said Sarah Ziegler, vice president of The MHE Research Foundation, which has provided seed funding for Dr. Yamaguchi’s research. “My son had more than a 100 of these tumors and has gone through 15 surgeries. When your child has such a debilitating condition, and you know there’s nothing you can do, it’s petrifying. Now we have hope.”
While this study takes MHE research a giant step forward, more questions remain. For one, it is still unknown how a few mutant bone cells can convince normal cells to divide and proliferate abnormally. Researchers hope that this MHE model will help solve that mystery, as well as provide leads for new treatments.
“This new mouse system also provides a platform for screening potential drugs that inhibit bone growths in MHE,” Dr. Yamaguchi explained. “We are currently developing chemical inhibitors to block their formation.”
10. Instances of Hereditary Multiple Exostoses (HME) in China, from 1990 – 2013
“...Hereditary multiple exostoses (HME) are an autosomal dominant skeletal disease with wide variations in clinical manifestations among different ethnic groups. This study investigated the epidemiology, clinical presentations, pathogenetic features and treatment strategies of HME in mainland China. We searched and reviewed the related cases published since 1990 by searching electronic databases, namely SinoMed database, Wanfang database, CNKI, Web of Science and PubMed as well as Google search engines. A total of 1051 cases of HME (male-to-female ratio 1.5:1) were investigated and the diagnosis was made in 83% before the age of 10 years. Approximately 96% patients had a family history. Long bones, ribs, scapula and pelvis were the frequently affected sites. Most patients were asymptomatic with multiple palpable masses. Common complications included angular deformities, impingement on neighbouring tissues and impaired articular function. Chondrosarcomas transformation occurred in 2% Chinese cases. Among the cases examined, about 18% had mutations in EXT1 and 28% in EXT2. Frameshift, nonsense and missense mutations represented the majority of HME-causing mutations. Diagnosis of HME was made based on the clinical presentations and radiological documentations. Most patients needed no treatment. Surgical treatment was often directed to remove symptomatic exostoses, particularly those of suspected malignancy degeneration, and correction of skeletal deformities. This study shows some variance from current literature regarding other ethnic populations and may provide valuable baseline assessment of the natural history of HME in mainland China.”
– Source: Guo XL, Deng Y, Liu HG, Clinical characteristics of hereditary multiple exostoses: a retrospective study of mainland chinese cases in recent 23 years. J Huazhong Univ Sci Technolog Med Sci. 2014; 34(1):42-50 – See more at: http://www.cancerindex.org/geneweb//X0205.htm
11. The following links http://www.cancerindex.org/geneweb//X0205.htm provides a detailed overview of ongoing HME-related research worldwide. A lot of research is now being conducted on mainland China with conclusions (as per the attached) highlighting that:
– “HME starts earlier and becomes more severe and extensive with each successive generation in members of the pedigree analyzed. A splicing mutation, IVS5+1G>A, of EXT1, first identified in Chinese population, may be responsible for HME in the studied pedigree. EXT1 and EXT2 mutation rates may be different between the Chinese and Western populations – See more at: http://www.cancerindex.org/geneweb//X0205.htm#sthash.JRl5abuL.dpuf“
12. Hereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments (June 2017)
“Hereditary multiple exostoses (HME) is a complex musculoskeletal pediatric disorder characterized by osteochondromas that form next to the growth plates of many skeletal elements, including long bones, ribs, and vertebrae. Due to its intricacies and unresolved issues, HME continues to pose major challenges to both clinicians and biomedical researchers. The purpose of this review is to describe and analyze recent advances in this field and point to possible targets and strategies for future biologically based therapeutic intervention.
Most HME cases are linked to loss-of-function mutations in EXT1 or EXT2 that encode glycosyltransferases responsible for heparan sulfate (HS) synthesis, leading to HS deficiency. Recent genomic inquiries have extended those findings but have yet to provide a definitive genotype-phenotype correlation. Clinical studies emphasize that in addition to the well-known skeletal problems caused by osteochondromas, HME patients can experience, and suffer from, other symptoms and health complications such as chronic pain and nerve impingement. Laboratory work has produced novel insights into alterations in cellular and molecular mechanisms instigated by HS deficiency and subtending onset and growth of osteochondroma and how such changes could be targeted toward therapeutic ends. HME is a rare and orphan disease and, as such, is being studied only by a handful of clinical and basic investigators. Despite this limitation, significant advances have been made in the last few years, and the future bodes well for deciphering more thoroughly its pathogenesis and, in turn, identifying the most effective treatment for osteochondroma prevention.”
Source / Author: https://www.ncbi.nlm.nih.gov/pubmed/284664532017 Translational Research Program in Pediatric Orthopaedics, Abramson Research Center, 902D, Division of Orthopaedic Surgery, Department of Surgery, The Children’s Hospital of Philadelphia, Philadelphia, PA, 19104, USA. email@example.com.
O’Reilly, with its variants Riley and R (e) illy, comes from the Irish Ui Raghallaigh, “grandson of Raghallach” thought to be from ragh meaning “race” and ceallach meaning “sociable”. The family was part of the Connachta tribal grouping and the particular Raghallach, and Irish chieftain from whom the name is derived is said to have been a descendant of the O’Conor kings of Connacht. A great-grandson of Maomordha, he lived at the time of Brian Boru, High King of Ireland, and, like him, died at the Battle of Clontarf in 1014.
The O’Reillys were for centuries the dominant ruling family of the kingdom of East Breifne, and at their height controlled most of counties Cavan and Longford and large parts of county Meath, despite many attempts by their main rivals, the O’Rourkes, to make it otherwise.
The chiefs were inaugurated on the Hill of Shantramon (Seantoman or Shantoman) between Cavan and Ballyhaise, in Castleterra parish on the summit of which may still be seen the remains of a Pagan Druidical temple consisting of three huge stones standing upright and known as Fionn McCool’s fingers. In later times the O’Reillys were inaugurated on the Hill of Tullymongan, above the town of Cavan; and took the tribe name of Muintir Maolmordha or the People of Maolmordha, one of their celebrated chiefs. This name Maolmordha or Mulmora was Latinized “Milesius” and anglicised “Miles” or “Myles,” – a favourite personal name among the members of the clan.
The patron saint of the O’Reilly family was St. Maedoc.
The Right Hand Symbol, a symbolic representation of God the Father in the Middle Ages, was the principal symbol of the clan.
The primary place of residence and Castle was Ballyreilly (Baile Ui Raghallaigh)
Their religious zeal is evident from the following foundations that were endowed by them: Monastery of the Augustinian Canons Premontre (Trinity Island, Lough Oughter, County Cavan, founded by Cathal O’Reilly, Prince of Breifne, circ 1237); Franciscan Monastery, Cavan town, founded by Gilla Isa Ruadh O’Reilly, King of Breifne, in 1300; Franciscan Brothers, Third Order Conventual, founded in 1414 by William O’Reilly at Thacineling, County Leitrim; Inchamore Abbey, Lough Gowna, County Cavan; while abbots of the O’Reilly family ruled the Monastery of Canons Regular of St. Augustine, Kells, County Meath from 1423 to 1523.
They were also renowned in medieval Ireland for their involvement in trade; their success may be gauged by the fact the “reilly” was at one point a colloquial term for money in Ireland, for the O’Reillys were the only clan in Ireland known to have a money system, their own coinage, which encroached on the monetary system of the English Pale and of Britain before being banned in 1447. What use they made of their prosperity can only be conjectured, but the phrase “the life of Reilly” is suggestive. After the collapse of Gaelic power in the seventeenth century, large numbers emigrated to serve in the armies of France, while many joined Colonel Edmund O’Reilly’s regiments in Austrian and Spanish armies during the 1700s.
The connection with the original homeland is still strong, however; even today (O’) Reilly is the single most numerous surname in both Cavan and Longford. The return of the prefix has been spectacular. Less than 10% give their name as “O’Reilly” in 1890, but almost 60% in 1996. The O’Reilly name is extremely common (as is Wang in China, or Kim in Korea) and widespread throughout Ireland, ranked the 8th most common in 1890 and 11th in 1996.
Myles Maolmordha O’Reilly, better known as Myles “the Slasher” O’Reilly fought his great fight as the heroic defender on the Bridge of Finea in Co. Cavan in 1644 where he and a band of one hundred held out against a 1,000-strong Cromwellian army. O’Reilly is commemorated by a cross in the main street of Finea, a pretty village on the banks of the River Inny.
Count Alexander O’Reilly (1722-1794) was born in Baltrasna, Co. Meath. Like so many of his “Wild Geese” generation, during the penal times he left Ireland and fight Spanish army. He became Governor of Madrid and Cadiz, and Captain-General of Andalucia. As a Field Marshal and Count, his later career took him to Cuba in 1769 to quell a rebellion. Many his of O’Reilly descendants are still to be found in Cuba. His name is recorded in one of Havana’s streets: Calle Orely.
The O’Reillys of Templemills, Celbridge, County Kildare: Pedigree
FATHER: Liam Sean O’Reilly, son of Dr. Michael William O’Reilly (http://wp.me/p15Yzr-R) I and Catherine Cooney, m. Kathryn O’Reilly, and had issue: Michael William III; Conor James; Niall Joseph.
GRANDFATHER’S BROTHER: Stephen James, son of John O’Reilly II, m. Elizabeth O’Toole (whose family have a tradition of descent from the O’Tooles of Wicklow) and had issue: Cathal; Elizabeth (Lilly).GREAT GRANDFATHER: John O’Reilly II, son of John O’Reilly I and Anne Craddock; m. Mary Lyons, and had issue: John Joseph; Stephen James; Michael William I;Mary Anne (Molly).
GRANDFATHER’S SISTER: Mary Anne (Molly), daughter of John O’Reilly II, m. Richard Eyre and had issue: Mary Una; Roland; Finbarr Roche; Margaret Elizabeth; William Joseph.
GREAT GREAT GRANDFATHER: John O’Reilly I of Templemills, Celbridge, born circa 1828-1832, son of Thomas Reilly and Anna Lynch, m. Anne Craddick (Craddock), 11 Oct. 1858 (Register of Celbridge), and has issue: John O’Reilly II and Michael O’Reilly.
GRANDFATHER’S FATHER’S BROTHER: Michael O’Reilly, m. Alice Barrett, and had issue: Edward Clement, Johanna Mary, Padraig Gabriel, Michael William, Angela, Margaret, and James Joseph.
GREAT GREAT GREAT GRANDFATHER: Thomas Reilly II, of Templemills, who m. Anna Lynch, circa 1812-1828, son of Thomas Reilly I of Templemills.
GREAT GREAT GREAT GREAT GRANDFATHER: Thomas Reilly I of Templemills, born circa 1792 son of James O’Reilly of Templemills.
GREAT GREAT GREAT GREAT GREAT GRANDFATHER: James O’Reilly of Templemills, born in County Cavan circa 1762-1777 (descended from Colonel Myles “the Slasher” O’Reilly) m. (Anne Gorey?), circa 1792.
As Colonel Myles died in 1644, there must be three or four generations missing between him and my GREAT GREAT GREAT GREAT GREAT GRANDFATHER James O’Reilly of Templemills.
Sons of the Slasher
The following is the pedigree of Colonel Myles O’Reilly, from Burke’s “Landed Gentry”, O’Hart’s “Irish Pedigrees, “The Dictionary of National Biography”, the Preface by O’Donovan to Carlton’s “Willie Reilly”, and the manuscript 23.D.9:-
Myles (Maelmordha) “the Slasher” O’Reilly m. Catherine O’Reilly and had issue: John, Philip, and Edmund.
From Myles “the Slasher” O’Reilly’s sons John, Philip, or Edmund, according to constant family tradition, is descended my GRANDFATHER Captain Michael William “M.W.” O’Reilly, I.R.A. 1916 (Commandant in P.H. Pearse’s division, holding the General Post Office during the Easter 1916 Rising against British rule in Ireland).
Alexander O’Reilly (Count Alexander de O’Reilly / Marshal Alejandro, Conde de O’Reilly)
Alexander O’Reilly was born in Baltrasna, Co. Meath in 1722. Military tradition ran in the family; his grandfather John O’Reilly was a colonel in the army of King James II, whose regiment—‘O’Reilly’s Dragoons’—fought at the siege of Derry.
Colonel John O’Reilly died on 17 February 1716. His wife was Margaret O’Reilly of County Cavan and they had five children, Brian, Eugene, Myles, Cornelius and Thomas.
The latter Thomas O’Reilly, father of Alexander, married Rose MacDowell of County Roscommon. Their four children were James, Nicholas, Dominic and Alexander.
Thomas O’Reilly left Ireland with his family and settled in Zaragoza, Spain where Alexander O’Reilly was educated. Aged only eleven, Alexander O’Reilly joined the Spanish army as a cadet in the Regimento de Infanteria de Hibernia, or Hibernia Regiment, formed in 1705. He was promoted to Sub-Lieutenant in 1739 (he was 17 years old), the year that war broke out with Britain and Austria. His regiment was sent to Italy to confront the Austrians. He showed such outstanding bravery and ability in several battles that he was promoted to Infantry Lieutenant. In the Battle of Campo Santo he was badly injured and lay all night on the field with other wounded and dead. The following morning, about to be bayoneted by an Austrian soldier, he convinced him he was of a wealthy Spanish family and worth a ransom. He was taken before the Austrian commander, who, as luck would have it, was another Irishman called Browne (Austrian military leader and scion of the “Wild Geese”, Maximilian Ulysses, Reichsgraf von Browne, Baron de Camus and Mountany), who had O’Reilly’s wounds tended to, and returned him to the Spanish side, but with a permanent limp as a result of his wounds.
Peace was signed and Alexander O’Reilly returned to Spain, now third in command of the Irish brigade Regimento de Infanteria de Hibernia or Hibernia Regiment. He immediately petitioned the king for a temporary transfer to the Austrian army, no longer at war with Spain, but now with Frederick the Great of Prussia. The Prussian army was renowned for its advanced tactics of manoeuvre and attack, and O’Reilly’s proposal was to study these with the view to their incorporation in the Spanish army.
In 1757 he joined the Austrian army, and distinguished himself against the Prussians at Hochkirchen, in 1758. The following year he entered the French service and assisted at the Battle of Bergen (1759), and the taking of Minden and Corbach.
War having broken out between Spain and Portugal, he re-entered the Spanish service, was made a Lieutenant-General / Brigadier, and defeated the Portuguese before Chaves, in 1762.
After campaigning in the Spanish invasion of Portugal not only was Alexander O’Reilly / Alejandro O’Reilly viewed as a fighting soldier, but also as an expert in military strategy and his recommendations for the tactical restructuring of the Spanish armed forces were approved. He subsequently swore allegiance to Spain and rose to become a Brigadier General.
Alejandro O’Reilly stayed acting as Adjutant and second-in-command for the new Governor of Cuba Conde de Ricla. While in Havana (Havannah), Ricla and O’Reilly received the city back from the British forces that had besieged and occupied it at the end of the Seven Years’ War.
Alejandro O’Reilly analysed what had gone wrong with the defenses of Havannah during the successful British siege in 1762, and recommended sweeping reforms to completely reorganise the defense of the island, while also calling for the introduction of a new justice system, increasing agricultural production, with a guaranteed market in Spain, and beef production. His recommendations were quickly approved by the Spanish Crown.
In 1765 he saved the life of King Charles III (King Carlos III) in a popular tumult in Madrid and was awarded by being sent Alejandro O’Reilly to Puerto Rico to assess the state of the defenses of that colony. Alejandro O’Reilly, known today as the “father of the Puerto Rican militia,” took a very detailed census of the island and recommended numerous reforms, including the instilling of strict military discipline in the local troops. He insisted that the men serving the defense of the Spanish crown receive their pay regularly and directly, rather than indirectly from their commanding officers, an old practice that had led to abuses. Some of O’Reilly’s recommendations resulted in a massive 20-year program of building up the Castle of Old San World Heritage Site.
Returning to Cuba, Alejandro O’Reilly married into a prominent Cuban family. His wife, Dona Rosa de Las Casas, was the sister of Luis de Las Casas, who served as Governor of Cuba. Today there is a street in Old Havannah “Calle Orely”, which is still named for O’Reilly, marking the location where this he came ashore while the English were embarking to leave.
Captain General of Louisiana
Alejandro O’Reilly was appointed Governor and Captain-General of colonial Louisiana while in Spain in April 1769, with orders to put down the revolt in Louisiana, and re-establish order.
Arriving in New Orleans from Cuba in August 1769, O’Reilly took formal possession of Louisiana. O’Reilly then held trials and severely punished those French Creoles responsible for the expulsion of Spain’s first Governor Antonio de Ulloa from the colony.
He is still remembered in New Orleans as “‘Bloody’ O’Reilly” because he had six prominent rebel Frenchmen executed in October 1769.
Having crushed the ringleaders who had led the Rebellion of 1768, O’Reilly turned his attention on administratively getting Louisiana back on its feet, and stabilising the food supply.
O’Reilly reformed many French bureaucratic practices and his proclamations and rulings affected many aspects of life in Spanish Louisiana, including the ability of slaves to buy their freedom, and the ability for masters to more easily manumit slaves. He also banned the trade of Native American slaves.
He regularized the weights and measurements used in marketplaces, regulated doctors and surgeons, and improved public safety by funding bridge and levee maintenance.
The affront to the self-esteem of the Spanish Crown having been quickly dealt with, and good public order restored, O’Reilly efforts had firmly positioned Louisiana as a dependency of the military and political establishment in Cuba.
Return to Spain
Back in Spain after October 1770, the king honoured O’Reilly with the title ‘Conte’ O’Reilly. He resumed his duties as Inspector General of Infantry, and then was named Inspector-General of Infantry and Governor of Madrid, which gave him control of all civil and criminal administration.
In 1775, O’Reilly was given command of a major Spanish expedition to Algiers, and it is said that jealously amongst the Spanish officers resulted in the ill-fated attack which left 2,000 soldiers dead and thousands injured. Although this North African campaign was a national humiliation, Alejandro O’Reilly was still held in high esteem by the king, who in 1776 appointed him Captain General of Andalucía and Governor of Cadiz, the key port connecting Europe with the Americas. He was very much at home in the political ambience of the time that was enlightened absolutism, and tight control from the centre attempting to resolve old ills and reform introduce reform. When he resigned in 1786 most of the people he worked with in Andalucía were full of praise for his energetic and authoritarian character as well as his special talent for implementing change.
He died in Bonete, near Albacete, Spain, in 1794, aged 72, while on his way to take command of Spanish force in the Eastern Pyrenees that had been ordered to resist, on behalf of French royalists, invading French revolutionary forces, following the beheading of Louis XVI during the French Revolutionary wars.
1). “The O’Reillys of Templemills, Celbridge and a pedigree from the old Irish manuscripts brought up to dat, with a note on the history of the clann Ui Raighilligh in general”
By E. O’H.
Published 1942 by Compiled and printed for M. W. O’Reilly Moorefield, Dundrum Co. Dublin Ireland.