Myasthenia Gravis need not be your fate.....

My name is Ninia, currently 34 years of age. Though Myasthenia Gravis, as I’ve learned from our research, can truly be life-changing, I wasn’t always afflicted with this disease. There was a time I didn’t worry about any disease at all, much less a cold. I lived healthy – neither smoked nor drinked, neither does my boyfriend then. I live actively as well. I should know what’s best, it comes naturally from being a Nurse (though I chose not to practice it and decided to be an entrepreneur).

My husband has always been supportive and kept an uplifting mind, all the while I struggled with the disease and even when I was beginning to wonder what was happening inside me that seemed so wrong.

I had a happy marriage, a content earning, and since we still don’t have kids we spent valuable time in dating and learning like two young lovers. I was as normal as anyone until 4 to 5 years ago, when one day I suddenly felt my knees give way, and during one occasion when watching a movie, my eyelids began to droop involuntarily. I began to feel nausea when I venture to a crowded place like in a mall even after a short amount of time, like being drowned in a sea of people.

MG makes one’s muscles very, very weak in more ways than one and in several periods of the day, if not all throughout the day. There were times at the height of my MG days that I needed my husband’s help in a lot of such simple activities like brushing my teeth, shampooing my hair, or helping me rise from my seat.

We consulted a lot of physicians: ophthalmologists, neurologists, general medicine, but each one seems to give just a mere piece of the puzzle. Determined to find a cause, we also tried to consult non-traditional methods only to find out that the idea of possible intervention of “unwanted spirits” and “other forces” would complicate matters more. MG, being an uncommon illness, is truly difficult to pinpoint, recognize, and treat. Until such time we came across a neurologist who thinks I MAY have a case of Myasthenia Gravis, but only after subjecting me to a number of special “tests,” all of which are expensive and are only available in modern hospital labs.

I underwent thymectomy on February 14th, 2007, after having one of the most critical decisions we’ve ever done. My doctor said the speed remission would be variable. And after several years, I am enjoying varying desirable effects. But none had been more dramatic than after trying an amazing product a friend has suggested.

Right now, I’m happy to know that even though MG may still be a lifelong predicament, I am free of the burden that MG has and might cause. This revolutionary product has helped me regain much of my normal life and it is my hope that it will do the same for you! Read on…

What is myasthenia gravis?

Myasthenia gravis is a chronic autoimmune neuromuscular disease characterized by varying degrees of weakness of the skeletal (voluntary) muscles of the body. The name myasthenia gravis, which is Latin and Greek in origin, literally means "grave muscle weakness." With current therapies, however, most cases of myasthenia gravis are not as "grave" as the name implies. In fact, for the majority of individuals with myasthenia gravis, life expectancy is not lessened by the disorder.

The hallmark of myasthenia gravis is muscle weakness that increases during periods of activity and improves after periods of rest. Certain muscles such as those that control eye and eyelid movement, facial expression, chewing, talking, and swallowing are often, but not always, involved in the disorder. The muscles that control breathing and neck and limb movements may also be affected.

What are the symptoms of myasthenia gravis?

Although myasthenia gravis may affect any voluntary muscle, muscles that control eye and eyelid movement, facial expression, and swallowing are most frequently affected. The onset of the disorder may be sudden. Symptoms often are not immediately recognized as myasthenia gravis.

In most cases, the first noticeable symptom is weakness of the eye muscles. In others, difficulty in swallowing and slurred speech may be the first signs. The degree of muscle weakness involved in myasthenia gravis varies greatly among patients, ranging from a localized form, limited to eye muscles (ocular myasthenia), to a severe or generalized form in which many muscles - sometimes including those that control breathing - are affected. Symptoms, which vary in type and severity, may include a drooping of one or both eyelids (ptosis), blurred or double vision (diplopia) due to weakness of the muscles that control eye movements, unstable or waddling gait, weakness in arms, hands, fingers, legs, and neck, a change in facial expression, difficulty in swallowing andshortness of breath, and impaired speech (dysarthria).

What causes myasthenia gravis?

Myasthenia gravis is caused by a defect in the transmission of nerve impulses to muscles. It occurs when normal communication between the nerve and muscle is interrupted at the neuromuscular junction - the place where nerve cells connect with the muscles they control. Normally when impulses travel down the nerve, the nerve endings release a neurotransmitter substance called acetylcholine. Acetylcholine travels through the neuromuscular junction and binds to acetylcholine receptors which are activated and generate a muscle contraction.

In myasthenia gravis, antibodies block, alter, or destroy the receptors for acetylcholine at the neuromuscular junction which prevents the muscle contraction from occurring. These antibodies are produced by the body's own immune system. Thus, myasthenia gravis is an autoimmune disease because the immune system - which normally protects the body from foreign organisms - mistakenly attacks itself.

What are myasthenic crises?

A myasthenic crisis occurs when the muscles that control breathing weaken to the point that ventilation is inadequate, creating a medical emergency and requiring a respirator for assisted ventilation. In patients whose respiratory muscles are weak, crises - which generally call for immediate medical attention - may be triggered by infection, fever, or an adverse reaction to medication.

STEPS ON HOW TO BUY AGEL PRODUCTS:
1. Go to www.agel.com (make sure that your country is indicated correctly on the upper left corner of the site.
2. Click "MEMBER'S LOGIN" (this function can be found on the upper right corner of the page.)
3. Click "PURCHASE PRODUCTS HERE"
4. Type this ID number: 712713 ( NINIA VERA )
5. Choose what product to order.
6. Supply the needed details, making sure you filled up all the necessary information.
7. Choose the product (1 box of EXO and 1 box UMI, since the products are sold per box, and each box is good for thirty (30) days of use)
8. You may pay for the products using your credit card.
Once paid, wait for the confirmation. The products will be delivered to your place.
Should you have anymore inquiries about the product or method of ordering, please feel free to email me @ jonivee2429@gmail.com. I hope this will be a start of something good for you, just like how I and a couple more people all over the world I knew and helped with Myasthenia, felt after using this product.
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