10 Best Type Of Bow For Hunting

Updated on: September 2022

Best Type Of Bow For Hunting in 2022


TOPARCHERY Archery Takedown Recurve Bow Hunting Long Bow Set Alloy Riser - Right Hand Black - Draw Weight 30lbs 40lbs - with Arrow Sight, Arrow Brush (Orange, 30lbs)

TOPARCHERY Archery Takedown Recurve Bow Hunting Long Bow Set Alloy Riser - Right Hand Black - Draw Weight 30lbs 40lbs - with Arrow Sight, Arrow Brush (Orange, 30lbs)
BESTSELLER NO. 1 in 2022

Diamond Archery Infinite Edge Pro Bow Package, Mossy Oak Country, Right Hand

Diamond Archery Infinite Edge Pro Bow Package, Mossy Oak Country, Right Hand
BESTSELLER NO. 2 in 2022
  • Wide draw length range between 13 and 31 inches
  • Accelerates arrows to up to 310 ft/sec
  • Redesigned cam system for a flawlessly smooth draw
  • Integral stabilizer creates a perfect balance and a steadier shot
  • Draw weight adjustable from 5 to 70 lbs of force

The Complete Guide to Hunting, Butchering, and Cooking Wild Game: Volume 1: Big Game

The Complete Guide to Hunting, Butchering, and Cooking Wild Game: Volume 1: Big Game
BESTSELLER NO. 3 in 2022

Vaorwne Archery Lightweight Canvas T-Type Bow Case Archery Hunting Crossbow Bag

Vaorwne Archery Lightweight Canvas T-Type Bow Case Archery Hunting Crossbow Bag
BESTSELLER NO. 4 in 2022
  • Bottom width: 69cm/27.2 (appr.)
  • Total length: 89cm/35.0 (appr.)
  • Material: Canvas
  • Color: Black
  • Shoulder strap length: 55 cm/21.6 (appr.)

Whitetail Adrenaline - The Reckoning Round 1 - All Public Land Whitetail Deer Bow Hunting

Whitetail Adrenaline - The Reckoning Round 1 - All Public Land Whitetail Deer Bow Hunting
BESTSELLER NO. 5 in 2022
  • Duration: 206 minutes
  • Not found on TV Anywhere
  • Grond Stalking Bow Edition
  • Real as we could film it - unscripted
  • Incredibly close shond long stalks

Outdoors with Eddie Brochin - The Real Deal - Hunting for Whitetail Deer

Outdoors with Eddie Brochin - The Real Deal - Hunting for Whitetail Deer
BESTSELLER NO. 6 in 2022

Atlantic Fleet

Atlantic Fleet
BESTSELLER NO. 7 in 2022
  • No In Apps/Advertising. No Pay-to-Progress. One Price = Full Game
  • Play the Royal Navy and her allies or Kriegsmarine in the Battle of the Atlantic
  • Single Battle Editor with 30 Historical Missions for standalone combat
  • Campaign of 50 missions per faction
  • Full Dynamic Campaign from 1939 to 1945

Primitive Archer

Primitive Archer
BESTSELLER NO. 8 in 2022

Traditional Bowyer's Handbook: How to build wooden bows and arrows: longbows, selfbows, & recurves.

Traditional Bowyer's Handbook: How to build wooden bows and arrows: longbows, selfbows, & recurves.
BESTSELLER NO. 9 in 2022

Salomon Men's Speedcross 4 Trail Runner, Black/Everglade/Sulphur, 10.5 M US

Salomon Men's Speedcross 4 Trail Runner, Black/Everglade/Sulphur, 10.5 M US
BESTSELLER NO. 10 in 2022
  • Agressive Grip : Obvious and penetrating traction on soft ground
  • Precise Foothold : Close to foot and comfortable feel
  • Contragrip rubber sole; MIDSOLE HEIGHT : 30mm/20mm (10mm drop);WEIGHT: 310g
  • Aggressive Grip : Obvious and penetrating traction on soft ground , minimalistic and strong lace for one pull tightening. Easy on, easy off
  • EVA midsole provides lighweight cushioning and stability

In the Darkest Shadows: Huntington's Disease

In the documentary, he compares her past young life; to her deterioration until age 40, where Huntington's disease has ravaged her mind and has made her nearly brain dead.

Huntington's disease affects the central nervous system causing intellectual impairment and severe mental disturbances. Initial symptoms include irritability, clumsiness, depression and forgetfulness. Eventually mood and personality changes occur combined with uncontrollable movements. It is a dominant gene, so as long as the victim has the gene, the person will have the disease, which is progressive and fatal, and carries with it a twenty year life expectancy after first showing symptoms. Huntington's specifically affects the number of repeats of CAG, three nucleotide bases, found at the end of the number 4 chromosome. This mutation increases the number of repeats to 37 or more, while a normal HD gene only has about 11 to 34 copies of CAG. The HD repeat size generally increases or sometimes dramatically increases from generation to generation when transmitted from one's father, but if transmitted from one's mother, only small increases or even decreases occur in the repeat size.

The article creates images of Huntington's which I have never truly heard or experienced of before. To me, reading about Huntington's disease or any type of disease in any biology book was dull and created insensitivity for any victims of the disease. Most biology books only go into details about how it affects the genes or what symptoms it creates, but how does this have to do about me. The article really addresses the day and the life of a Huntington's carrier, and hits more to home because a true individual is spoken of and makes me realize this experience can become a personal experience. Also, it is written using regular vernacular, rather than any technical, scientific language to describe the victim and his troubles. I prefer learning about any disease through the context of an actual individual rather than through the use of definitions. It makes the word, Huntington's, an actual disease, rather than a definition in a dictionary or glossary in the back of our biology book. It makes the word, Huntington's, a disease to be scared of having, rather than a word not worth reading. Through the use of personal stories, the reader is able to get a sense of the overall disease and the experiences which surround it. It demonstrates a gradual and progressive disease that changes over a person's life, giving a true sense of time and making the disease that much more real, especially to those who have not experienced it. The background on the disease was helpful though, more so to researchers than average people.

The article is a bit outdated as of today. The background on the disease is about eleven years old and there may be new findings as to how Huntington's disease is operated or treated that I would like to know more about. I would think that the tests have also become easier and more efficient and thus less expensive for any Huntington's disease victim, not unless the actual tests have gotten more complex and sophisticated and keep the costs pretty level. It is surprising to me that with all our technical and scientific expertise with the genome that there is not identifiable cure to date or some sort of medicinal aid to increase the life span of a Huntington's carrier. I understand there are probably stimulants designed to lessen the impact of carrier's lost mental capacity, but how come there are no other drugs, which have lowered the fatalities of Huntington's disease carrier. It may be due to the repeat CAG mutations, but would that really prolong the research of a working treatment to combat the terrible effects of Huntington's?

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