All Posts Tagged With: "muscle pain"

Linda’s comments: Linda’s comment:  This is the reasons why I try and guide people to make their own healthcare choices and learn all they can about holistic/alternative medicine….There are wayyyyyyyyyy to many folks with Lyme disease who are given these products…..<sigh>

link: http://www.medicationsense.com/fluoroquinolone.html 

Excerpt:

Levaquin and Cipro Reactions

In 2001, Dr. Jay S. Cohen published a ground-breaking article* on the severe and often disabling reactions some people sustained while taking Levaquin, Cipro, or another FQ antibiotic. Dr. Cohen says, “It is difficult to describe the severity of these reactions. They are devastating. Many of the people in my study were healthy before their reactions. Some were high intensity athletes. Suddenly they were disabled, in terrible pain, unable to work, walk, or sleep.” 
The 45 subjects in Dr. Cohen’s study reported the following side effects*.

Peripheral Nervous System

: Tingling, numbness, prickling, burning pain, pins/needles sensation, electrical or shooting pain, skin crawling, sensation, hyperesthesia, hypoesthesia, allodynia (sensitivity to touch), numbness, weakness, twitching, tremors, spasms.

Central Nervous System:

 

Dizziness, malaise, weakness, impaired coordination, nightmares, insomnia, headaches, agitation, anxiety, panic attacks, disorientation, impaired concentration or memory, confusion, depersonalization, hallucinations, psychoses.

Excerpt:

If you have multiple sclerosis (MS)––or you know someone who does––you probably remember how long it took to make the diagnosis.  You also may remember a lot of blood tests, a lumbar puncture, at least one magnetic resonance imaging (MRI) scan, as well as many visits and examinations by various doctors.  You may wonder why it still takes so long to make the diagnosis in this modern age of MRIs and other sophisticated tests.  We are going to try to explain why it can be so difficult for even the most expert MS neurologist to determine that someone has MS.  You have to live with the diagnosis and face the disease and the treatments.  You should understand and have confidence in the diagnosis.  Also, if your case of MS does not fit the typical pattern, you need to be aware of the other disorders that can mimic MS.  This is important because the treatments may be very different and, just as in most cases of MS, treatment begun early in the course of the disease is the best way to prevent or slow further neurologic damage.

MRI and new laboratory tests have definitely helped speed the diagnosis, but it still takes longer than anyone would wish, even in easy cases.  This is partly because of the variable nature of the disease in its many signs and symptoms. But it is also because a rather long list of other medical disorders can cause neurologic symptoms and signs that resemble MS. Furthermore, the “white spots” on brain MRI can be caused by a number of other conditions that also need to be ruled out.

The diagnosis of clinically definite MS requires that a person experience at least two neurologic symptoms of the type seen in MS, in two different areas of the central nervous system (CNS), at two different times (‘disseminated in space and time’).  Most typically, the symptoms are optic neuritis plus either an abnormal sensation or a problem with movement.  It can also be numbness in one part of the body and weakness or lack of coordination in another.  But in every case, there can be no other explanation for the symptoms, the changes seen on the MRI, and the abnormalities in the spinal fluid.  Many “mimics” need to be ruled out in order to make the diagnosis of MS. 

Human leptospirosis can be a difficult infection to describe, as the
symptoms can vary dramatically between patients. Some symptoms are
extremely common, but only a small number of patients will experience
the severe life-threatening illness known as Weil’s disease. The
severity of the infection depends on the age and general health of the
patient, plus the serovar (strain) of bacteria involved and the number
of bacteria that entered the patient’s body. Continued

Clinical practice guidelines are increasing in number. Unfortunately,
when scientific evidence is uncertain, limited, or evolving, as is often
the case, conflict often arises between guideline committees and
practicing physicians, who bear the direct responsibility for the care of
individual patients. The 2006 Infectious Diseases Society of America
guidelines for Lyme disease, which have limited scientific support,
could, if implemented, limit the clinical discretion of treating physicians
and the treatment options available to patients

Introduction

Clinical practice guidelines are now ubiquitous throughout the
United States. The National Guidelines Clearing House, under the
category “diseases,” currently lists 2,126 separate guidelines on its
web site. Clinical guidelines are intended to assist physicians in
patient care by clearly communicating the results of the guideline
committees’ evaluation of available therapeutic options. However,
the processes by which individual guidelines are constructed may be
less clear, leading to disagreements between the issuing committee
and the physicians who treat patients-physicians who may well be
as experienced and knowledgeable as the guideline committee. Continued

Linda’s Comment:  It amazes me that in the following publications do we find any suggestions about reducing our total body burden of pathogens and toxins.  It is a MUST that Lymies begin to reduce their total body burden of pathogens and toxins in order to begin addressing Lyme, Lyme Arthritis, Arthritis, and other chronic illness we see with Lyme patients.  Some people choose antibiotics…..I personally never went near antibiotics.  My whole detox and healing program was using anti-microbials, alternative medicine, alternative modalities, NO GMO foods, NO sugars, NO fast foods, NO soda’s, NO caffeine, NO coffee and I ate and still do eat organic foods.  I also have used a PhotonGenie since 2001 and use it daily.  I like it better than Rife, as I don’t have to worry about settings, I just turn it on and go.  I even sleep in mine.  The critters we Lymies fight LOVE heavy metals and especially GMO foods.  
 
There are also some foods that you don’t want to eat if you are having symptoms of Arthritis, however, it is more important to get rid of the GMO, sugars, coffee and soda’s to reduce the inflammation and pain.  The great thing about the fight program is you are dissolving biofilms and reducing inflammation on a daily basis.  So much of our pain comes from inflammation. 
 
I of course use many more things with my lifelong daily detox protocol.  If you can get IV chelation and do weekly colonics you can move things along faster.  However, you can start the program one step at a time and move at your own pace.  This is one protocol that must be done as suggested to get the full benefit of wellness.  The first three months are your toughest, but after that it is a breeze.  Yes, ever so often you have a day or two like you did when you first started, but I tell folks, it is like peeling an onion.  As you reach a new level you will have a couple of days where you keep your bathroom close.  At the end of 60 to 90 days and you begin to feel your life coming back to you, you will be very pleased that you began this journey.  Feel free to ask questions and I will share my journey with you.  Just remember JUST SAY NO TO GMO!! Continued