Sunday, February 25, 2018

iPhones Have Been Keeping These Secrets For Too Long

http://www.fashionbeans.com/content/iphones-have-been-keeping-these-secrets-for-too-long?rtg=3166-lkm03L¶m4=fsb-fni-fbss-3166-us-mo-ocpm-look75¶m5=10154383474101186¶m6=23842743793100652

On-board compressed air (#5) - 4x4Help.com

On of several articles at this site - this has a good description of the many small parts required:
http://4x4help.com/tech/oba5.htm

On-board compressed air #3 - 4x4Help.com

One of several similar articles at this site - this has a good set of photographs:
http://4x4help.com/tech/oba3.htm

On-board compressed air - 4x4Help.com

One of several articles on this site - it has a comprehensive parts list:
http://4x4help.com/tech/oba4.htm

Axles and What Vehicles they came in - www.4x4Help.com

http://4x4help.com/axle/axlevehicles2.htm

Axle identification - 4x4Help.com

http://4x4help.com/axle.htm

Ford Explorer rear axle measurements & details - 4x4Help.com

These are often recommended for Falcons & Mustangs as well as Jeeps.. From 1995 on they feature disc brakes, and can be found with limited-slip differentials and various gear ratios.

The Ford 8.8-Inch Solid Rear Axle: 
https://www.therangerstation.com/tech_library/Ford-8_8-axle.shtml
"Axle Width Differences:
1990-1992 Ford Ranger 8.8-Inch Axle - 56.50 inches
1993-2009 Ford Ranger 8.8-inch Axle - 58.50 inches
2010-2011 Ford Ranger 8.8-inch Axle - 58.50 inches *
1991-2003 Ford Explorer 8.8-Inch Axle - 59.625 inches
* The 2010-2011 Ford Ranger 8.8-inch axle is actually narrower and has shorter shafts than the 2009 and earlier models. Ford used rear disc brakes on the 2010-2011 Rangers, so Ford Shortened the axle housing and shafts to compensate for the extra width created by the disc brake setup. These shafts are not going to work in a 2009 and older Ford Ranger 8.8-inch axle. "

2010 Ford Ranger 8.8-Inch Axle vs 2004 8.8-Inch Axle:
https://www.therangerstation.com/tech/2010-ford-ranger-8-8-inch-axle-vs-2004-8-8-inch-axle/

The Ford Explorer 8.8-Inch Rear Axle - Swap:
https://www.therangerstation.com/tech_library/Explorer8_8.shtml

How wide is a Ford 8.8 rear end?  https://askinglot.com/how-wide-is-a-ford-88-rear-end
"Vehicle Application        Axle Width (inches)
'86-'93 Ford Mustang 8.8     59 11/44
'65-'66 Mustang        57 11/44
'67-'70 Mustang 8.0        59 51/48

Axle Dimensions        Ranger 1983-1992 7.5-Inch Axle     Explorer 8.8
Width WMS-WMS         56-1/2 inches             59-1/2 inches
Axle tube diameter (1983-2009)     2.80 inches             3.25 inches"

8.8 Axle Facts and Swap info:
https://www.explorerforum.com/forums/threads/8-8-axle-facts-and-swap-info.235261/
"Explorer 8.8 Measurements:
Weight (complete assembly w/ brakes etc.): 174 lb.
O.D. of tubes: 3.250".
Tube thickness: .250" (some are .188”!)
Ring gear diameter: 8.800".
Ring gear bolts: 7/16" dia. (qty. 10).
Pinion diameter/splines: 1.625 / 30.
Axle shaft/splines: 1.320 / 31.
Rotor thickness (where it mounts to axle is .250").
Overall width 59.625" (the F8.8 is .950" narrower then a TJ Dana 35).
(The F-150 8.8 is drum brake and width WMS to WMS is 65.5”.)
Hole diameter for ABS sensor in top of housing: .811".
Bolt size (U-joint flange to yoke) is: 12 x 1.75 x 30 mm
Centerline of housing to C/L of pinion difference is 3.875" toward the P/S.
Pinion offset: P/S to C/L of Pinion, 27-3/4" (no rotor on axle), D/S to C/L of Pinion, 31-5/8" (no rotor on axle). (this measurement is 2.5" more offset to the P/S then a TJ Dana 35).

Specs:
Code Capacity Ratio
43 Open 3200 3.08
41 Open 3200 3.27
42 Open 4.10
46 Open 3.73
45 Open 3200 3.55
D4 Limited Slip 3200 3.73
D2 Limited Slip 4.10
L73 Limited Slip 3.73
L - Limited Slip Differential
C - Conventional Differential

How many splines are the axle shafts?
31 spline for 97 & up Mountaineer, 95 & up Explorer - 30-1/2 inch length - 5 X 4.5 inch lug pattern.
31 spline for 97 & up Mountaineer, 95 & up Explorer - 27-5/8 inch length - 5 X 4.5 inch lug pattern"

Rear End Widths:  http://www.carnut.com/specs/rear.html
A chart listing specifications for the major American cars & trucks back to the mid '60s.

Scrounger’s Guide - Ford 8.8 Rear Axle:  https://www.motortrend.com/how-to/ford-rear-axle/



Tuesday, February 13, 2018

Sunday, February 11, 2018

FORD Complete TBI system | Affordable Fuel Injection

For classic Ford small blocks:

https://affordable-fuel-injection.com/product/ford-complete-tbi-system/ 

 Base price (in 2021) $845 - with necessary options (distributor, fuel pump, etc.) $1,139.00 or more.

Howell EFI Conversion & Wiring Harness Experts – EFI Is All We Do

Upgrades for classic vehicles:
https://howellefi.com/

Monday, February 5, 2018

Diabetic Brains - Nemechek Autonomic Medicine

https://www.nemechekconsultativemedicine.com/blog/diabetic-brains/

From FB post:

Diabetic Brains

By Dr. Patrick M. Nemechek, D.O. and Jean R. Nemechek

The common form of diabetes (DM II) that affects 11-24% of the U.S. adult population is commonly discussed as a problem of elevated blood sugar primarily caused by obesity. Unfortunately, this version is very outdated.

A steady stream of research is demonstrating that diabetes is a chronic condition resulting from the deterioration of brain function. Brain function deteriorates, and then the symptoms of obesity and abnormal blood sugar regulation follow.

Unrepaired damage to the brain sets into motion the deterioration of the body. People need to be aware of the effects diabetes has on the brain and the aging process as measured by Autonomic Nervous System testing.

More importantly, people need to know that the Autonomic Nervous System is now capable of improvement or repair.

The Autonomic Nervous System is the brain's communication network that regulates hunger, where and how body fat is deposited, many hormones including insulin, and the hunger hormones leptin and ghrelin.

When Autonomic Nervous System function deteriorates the brain's hunger, glucose regulation, and body fat regulation systems falter. This is when body fat increases and blood sugar levels rise.

Increased levels of hunger, thirst, abdominal fat, fatigue, blood sugar and blood pressure regulation problems are the result of Autonomic Dysfunction from metabolic inflammation. Simply put, these are symptoms of brain deterioration due to increased inflammation.

Diabetics are suffering from premature aging of their brains with deterioration of their Autonomics, up to a 50 – 80% reduction of Autonomic Nervous System function over the first two decades.

In other words, diabetics may reach Stage 5 Autonomic Dysfunction, cardiac autonomic neuropathy ("CAN"), nearly two decades earlier than people who are their same age who do not have diabetes.

The rapid aging of diabetic brains is easily measured through Autonomic Nervous System testing. It is important to detect and stabilize advanced Autonomic dysfunction because CAN, if left untreated, has a 50% mortality rate in 5 years.

The importance of Autonomic testing to identify CAN is not new information to the medical community. In the 2010 Standards of Care the American Diabetes Association stated that screening for signs and symptoms of cardiovascular autonomic neuropathy (CAN) should be instituted at the time of diagnosis of type 2 diabetes and within 5 years after the diagnosis of type 1 diabetes (Diabetes Care, Volume 33, Supplement 1, January 2010, page S37).

Yet many diabetics and their physicians have never heard of cardiac autonomic neuropathy even though it is responsible for sudden death syndrome, the most common form of death for diabetics.

Education about the diabetic pathway may help people take steps to prevent the disease.

How do we know if we have developed type II diabetes? Many people become aware of the disease process when blood sugar test numbers identify them as "pre-diabetic" which is a state of impaired glucose tolerance.

This is an important window of time in which substantial changes to one's diet can halt or reverse the impaired glucose tolerance process, such as dropping one's daily total intake of carbohydrates and sugar below 100 grams a day.

Four words sum up the disease at this point: diabetes is carbohydrate poisoning. Diet is so important that the medical treatment for diabetes back before the invention of insulin was … a low carbohydrate diet.

But today too many people misunderstand this phase and think they are "just" pre-diabetic on blood work so they "wait" until their numbers get worse to "do" something (pills or insulin).

But in the pre-diabetic stage people have already begun to experience decreased Autonomic Parasympathetic modulation of their heart. That means in pre-diabetics their brain has already started having trouble controlling their heart through the Autonomic Nervous System.

Valuable time is lost when someone waits to pass from being pre-diabetic to the diabetic range on a lab test. That lab result is simply a number on a piece of paper that alerts us when excess sugars in the body transition from being toxic to the sugars that actual cause a disease themselves.

People may better understand what is going on within their body if they choose the most informative blood test. There are two blood tests that are given to check for diabetes and people should know the difference so that they can request the Hemoglobin A1c test that is newer and more accurate.

Poorly trained healthcare professionals either do not understand the tests or they do not understand the bigger picture of disease and organ damage.

The first testing method is the old Fasting Blood Sugar testing on a basic blood panel, but this test is limited and only measures the liver's ability to properly make or maintain blood sugar while sleeping the night before your test. It does not reflect what will happen after you eat, like how high or how low your sugars will go.

The other test, which is just minimally more expensive, is the Hemoglobin A1c. This test is the most accurate measure of glucose regulation because it averages your blood sugar over the last 3 months. It is the measure of advanced glycation end products ("AGE's") from elevated blood sugars.

With only a limited look at blood sugar (fasting blood sugar), and not an extended 3 month look at blood sugar (HgbA1c), many people do not realize they are slipping into pre-diabetes and their opportunity for prevention and intervention are lost.

An A1c of 5.6 or less is normal, 5.7 – 6.4 is pre-diabetic, and 6.5+ is diabetic. But when someone reaches 6.5 and is officially diagnosed with diabetes half of their pancreas has already been destroyed. The blood tests are way behind the silent destruction.

The second part of understanding the diabetic brain is found in a network called the Autonomic Nervous System. The Autonomics control every organ in the body such as the heart, bladder, stomach, intestines and kidneys. It is how the brain regulates blood pressure, blood sugar, sleep cycles, the immune system, and hormones.

There are two main branches in the Autonomic Nervous System. In simple terms, the Sympathetic branch is responsible for energy expenditure ("fight or flight") and the Parasympathetic branch is responsible for energy conservation and restoration ("rest and digest").

These two opposite Autonomic branches should work together simultaneously and in balance. But number of things are damaging the Autonomic Nervous System and causing patterns of weakness or excess in one or both branches too early in diabetics.

Autonomic function naturally declines with age but it has become clear to me over the past 11 years that our Autonomics have become increasingly prone to injury and dysfunction after some accumulation of stress, poor nutrition, chemicals in our foods, childbirth, intestinal infections, and both physical and emotional concussions and traumas.

When the Autonomics fail to work properly the bodies' response to disease and stress are impaired. The brain develops problems that include maintaining normal heart rhythms, blood pressure and brain oxygen delivery, moving the digestive tract, and proper organ and immune function.

If the "fight or flight" Sympathetic brain commands are disrupted people may feel tired, crave salt or sugar, experience excessive hunger, or get anxious.

People may get heart palpitations, tingling or numbness in their arms (hands or face), disrupted night vision, varicose veins, E.D., stiff necks and shoulders, severe ("migraine") headaches, or insomnia.

If the "rest and digest" Parasympathetic brain commands are disrupted they may affect the intestinal tract (heartburn or constipation), immune system (autoimmune disorders), and produce chronic pain syndromes (fibromyalgia).

People may get sleep apnea, "restless legs", morning nausea, night sweats/hot flashes, power surge sensations when they should be at rest, or non-restorative sleep.

There are five stages in Autonomic Dysfunction and in Stage 3 people start to experience symptoms that affect their daily life like GI trouble, sleep trouble, headaches, temperature regulation problems, or dizziness.
Stage 4 and Stage 5 Autonomic Dysfunction are the results of progressive deterioration.

Spectral analysis Autonomic testing measures the weakening of one or of both the Autonomic branches. This is important diagnostic information for diabetics to know because they may develop weak Autonomic patterns years or decades too early than the natural rate of aging.

Extreme Autonomic imbalance, which is Stage 5 Autonomic Dysfunction, is cardiac autonomic neuropathy (CAN) which has a 50% mortality rate in 5 years. This Autonomic pattern places diabetics at risk of cardiac events, including during times that the Autonomics are artificially suppressed like when someone has gone to sleep under anesthesia.

Diabetes pre-maturely accelerates the ability of the brain, through the Autonomic Nervous System, to properly control the heart (leading to CAN = increased risk of sudden death). To reverse CAN and restore normal aging Autonomic Nervous System balance must be restored.

The first step is to identify Autonomic Dysfunction and CAN and then stabilize with medication when necessary. The second step is to lower metabolic inflammation in the body and brain with every tool available. The lowering of inflammation is greatly accomplished by key shifts in diet, food quality, and methods of cooking. This is how people make their kitchens more powerful than the operating room.

Metabolic inflammation is the cumulative effect of a variety of problems. Excessive omega-6 fatty acids (vegetable oils) and deficient omega-3 fatty acids (DHA, ALA, EPA) in our foods are believed to be one of the major global triggers of obesity and diabetes.

Compounding this is an imbalance of intestinal bacteria (SIBO) and the ingestion of chemicals referred to as AGE's (advanced glycation end products).

AGE's are formed from heating sugar and protein molecules at high cooking temperatures, and are often found in commercially prepared foods. The higher and longer the temperature during cooking, the more AGE's are formed. Simply cooking foods at lower levels results in lower blood sugar levels for diabetics.

If you are diabetic or pre-diabetic, you need to reduce your levels of inflammation to maintain a brain that can function more normally. By lowering inflammation enough, your Autonomic Nervous System can recover, and this improvement can lead to a reduction in blood sugar, blood pressure, hunger levels, and body weight.

Fixing the brain, to fix the body, takes persistent effort by the patient but I have guided Autonomic recovery even in diabetics who presented in my office in advanced Stage 5 Autonomic Dysfunction. I am an internal medicine physician (D.O.) from UCLA and my Internal Medicine and Autonomic practice is in the Phoenix area.

I use Vagal Nerve stimulation in my medical practice, and I have discovered a multifaceted formula for Autonomic restoration that is so groundbreaking that I recently filed a patent application for The Nemechek Protocol for Autonomic Recovery (Patent Pending). For additional information you may call my office 623-208-4226 or go to AutonomicMed.com

Remember, it is the failure of the brain is that sets into motion the failure of the body. And we can, reverse CAN.

This post is provided as an information resource only, and is not to be used or relied on for any diagnostic or treatment purposes. This information is not intended to be patient education, does not create any patient-physician relationship.

© 2016. Dr. Patrick M. Nemechek and Jean R. Nemechek. All Rights Reserved. Patent Pending.