


"This Coat of Arms was prepared by the Department of Heraldry of Tiffany, New York, and was considered by Francis Bacon Trowbridge to correctly depict the Trowbridge Coat of Arms. It reads in Latin: "Let the bridge be firm." The Trowbridge Coat of Arms in England was borne, by Admiral Sir Thomas Troubridge (as it was spelled then): a brave naval officer under Horatio Nelson, Great Britain's greatest admiral. Sir Thomas Trowbridge was knighted in 1799. The cross keys of St. Peter being added to his Coat of Arms after his reduction of the Castle of Saint Elmo. His motto was SPES PONS VITAC ESTE. The Trowbridge Coat of Arms was still on a wind.. in St. James Church, Taunton, England in 1908."

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This
web page is primarily about
the descendents of David Trowbridge (b. 1709), which settled in
Morris County sometime during the 1730s. Many of David's
descendents now live throughout the United States. If you were to do
a web search on Trowbridge genealogy, you wil find a significant
portion of web pages are about his descendents. This web site
is primarily is about the branch of the family that remained in
Morris County. In researching this web page, I
relied on
a variety of sources, including such genealogy web sites such as
Ancestry.com, Family Search.com, other Trowbridge web pages
(especially the web pages of cousin Cheryl Trowbridge-Miller,
&Sylvie
Higgins Paine), research by two of my second cousins, Mary Pavlik and
Doug Gawron; the US Genweb pages for Morris County (maintained by
Brianne Kelly-Bly); local cemeteries, libraries.
The most
important source of most of this information is the book that has
become the main source book of information for Trowbridge
researchers, "The Trowbridge Genealogy" by Francis Bacon
Trowbridge. Francis Bacon Trowbridge, was a New Haven based
genealogist from the early part of the 20th century who compiled this
book in 1909, following the mass mailing of about 800-1000
questionnaires to members of the Trowbridge family living throughout
the United States. The information that he obtained is an invaluable
source of information for Trowbridge researchers. If
you
wish to obtain a copy of "The Trowbridge Genealogy", it
is available as a free PDF download
through the Internet Archive Project,
courtesy of Microsoft and the Allen County Public Library of Ft.
Wayne Indiana.
Trowbridge,
the name
in early records is variously spelled: Troubrugge, Trobrugge,
Troubrigge, Troubryge, Troubbridge, Troubridge, Troberidge,
Trobrydge, Trobreeg, Troobridg, Troblebridge, Trobblebridge,
Throughbridge, Throwbridge, Trobruig, Trobridge, Trowbrydge,
Sturbrigge, Sturbridge, Turbridge, Strobreidge, Strobridge,
Strowbridge, Strawbridge, (the final "e" being omitted in
many cases). The mode of spelling now generally adopted is
Trowbridge. Trowbridge has been used as a surname in England for many
centuries, but the exact time that it was first so used is uncertain
and the Authors of dictionaries of family surnames do not agree as to
its derivation. Bardsley in his "Dictionary of English and Welsh
Surnames" states that the name was first given an individual on
account of his residence at Trowbridge in Wiltshire. It may be said
that this was its origin, and that a member of the family removed to
Devon and gave the same name to his seat in that county, and it is
also quite possible that some individuals in later times may have
assumed the name of Trowbridge on account of a residence at
Trowbridge.
Trowbridge is a thriving market town situated on a rocky eminence rising from the valley of the river Biss, and in respect of population is the largest town in Wiltshire. The parish of Trowbridge forms part of the hundred of Melksham. On the south side it adjoins the hundred of Wherwelsdown and on the west of that of Bradford-on-Avon. It consists of a strip of land some three miles long and on an average one mile broad, and contains in all 2,443 acres. It is divided into several tithings; on the north is that of Staverton; on the west that of Trowle; on the south that of Studley; and there is also the town Liberty. The town itself is situated, as nearly as may be, in the center of the whole parish. No trace of history of Trowbridge is found until the end of the eleventh century, here we find it in the Domesday book, where it is called Straburg; a strange form of the name, but nevertheless pretty clearly identified with what we now call Trowbridge.
Wiltshire,
LXVII: The
Land of Oda And Other Kings Theghs, Page 192
"Beorhtric holds
Trowbridge his father held it in Trey, and it paid geld for 10 hides.
There is land for 9 ploughs. In demeshe are 2 ploughs and 7 slaves;
and 11 villains and 6 cotsets with 7 ploughs. Ther is a mill
rendering 10s and 10 acres of meadow, and 12 acres of pasture. [And]
woodland 5 furlongs long and 3 furlongs broad. It is worth 5 pounds
now 8 pounds."
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The following is a description of CMT from the
Charcot-Marie-Tooth Association website:
"...Charcot-Marie-Tooth, or CMT, is the most common inherited
neurological disorder, affecting approximately 150,000 Americans.
CMT is found world-wide in all races and ethnic groups. It was
discovered in 1886 by three physicians, Jean-Marie-Charcot,
Pierre Marie, and Howard Henry Tooth.
CMT patients slowly lose normal use of their feet/legs and
hands/arms as nerves to the extremities degenerate. The muscles
in the extremities become weakened because of the loss of
stimulation by the affected nerves.
Additionally, there is a loss of sensory nerve function. Unlike
muscular dystrophy in which the defect is in the muscles, CMT is
a disorder in which the defect is in the nerves that control the
muscles.
What are its characteristics?
A high arched foot is one of the first signs of this disorder. As
the disease progresses, structural foot deformities take place.
The patient develops a pes cavus foot with hammer toes. Foot drop
and ankle sprains are frequent manifestations. The progressive
muscle wasting leads to problems with walking, running, and
balance. To avoid tripping, patients with foot drop raise their
knees unusually high resulting in high steppage gait. In some
patients, muscle weakness may also occur in the upper legs. Flat
foot is seen as well in patients with CMT.
Hand function also becomes affected because of progressive muscle
atrophy, making fine manipulatory acts, like writing,
difficult.
The loss of nerve function in the extremities also leads to
sensory loss. The ability to distinguish hot and cold is
diminished as well as the sense of touch.
CMT also can be inherited in a recessive or an X-linked pattern.
The degree of severity can vary greatly from patient to patient,
even within the same family. A child may or may not be more
severely disabled than his/her parent.
How is it inherited?
CMT is generally inherited in an autosomal dominant pattern. This
means that if one parent has the disease (either the father or
the mother) there is a 50% chance of passing it on to each
child.
CMT can also be inherited in recessive or an X-linked pattern. To
determine the pattern of inheritance, each CMT patient should
consult a genetic counselor, neurologist or other medical
authority familiar with the disease.
How is it diagnosed?
Careful diagnosis of CMT involves clinical evaluation of muscle
atrophy, testing of muscle and sensory responses, nerve condition
and electromyographic (EMG) studies, as well as a thorough review
of the patient's history. CMT types 1A and 1X can now be
diagnosed by a DNA blood test. Some people who carry the CMT
genetic trait show no apparent physical symptoms. The variation
in degree of physical disability, together with a lack of
physician awareness of CMT, has often led to misdiagnosis.
Today, the Charcot-Marie-Tooth Association is educating both
medical specialists and patients about CMT.
How is it treated?
At present there is no cure for CMT, although physical therapy
and moderate activity are often recommended to maintain muscle
strength and endurance.
Custom shoes or shoe inserts (foot orthoses) will help to improve
gait. Leg braces will prevent ankle sprains, improve gait, and
reduce the amount of energy needed to walk. Corrective orthopedic
foot surgery is available to help maintain mobility when
medically indicated.
Splinting, specific exercises, adaptive devices and surgery can
help maintain hand function.
Currently I am trying to track the extent of the disease in the
Trowbridge family, namely those descended from David Trowbridge
and Anna Youngs of Mount Freedom, New Jersey. If you or any
members of your family who suffer from this disease, or any of
the symptoms, you can email me at trowbridges@gmail.com. For more
information on CMT, visit the above linked website. You can also
get more information from the Muscular Dystrophy Association
(MDA) website by clicking here.

Special thanks to the following
members of the Trowbridge family who contributed to this
webpage:
the late Barbara Foderaro for information on the descendents of
William Francis Trowbridge
Angela Dethloff for her hours of
research, and information on her ancestor, William Francis
Trowbridge's brother, David Jarrard Trowbridge.
Nancy for
information on Thomas Trowbridge.
George Trowbridge, Sr. and
Cherri Trowbridge for information regarding the family of Elwood
Trowbridge and Rose Snook.
Cheryl Trowbridge-Miller for material
regarding Charles Tyler Trowbridge and the descendents of David
Trowbridge the son of Daniel Trowbridge.
Charlie Scott (Tabitha
Trowbridge)
Doug Gawron (documents and theories regarding Shubael
Trowbridge &Crispus Trowbridge)
Mary Pavlik (The descendents
of David J. and Bryant Trowbridge)
Jim McCallum (Crispus
Trowbridge and the Canadian branch of the Trowbridge family)
Cristi
Starr (Strawbridge and Maus families)
George S. Nas
and many
others, who are acknowledged throughout my webpage.

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