No treatment for Myasthenia Gravis is good for all; a special program should be created for each patient considering their age, gender and the intensity of the symptoms. Below listed are the most commonly applied and trusted treatments, I have also included my own experiences about the ones I have tried.

Cholinesterase (ChE) Based
Although these show improvement in many patients, they have no effect on some. The symptoms disapper or vanish for a short term; this changes from patient to patient, but from my experience I can say that it is between 4 to 6 hours. Only you can decide how often and how many at a time you will take of these pills, someone from the outside (even a doctor) can not give you a completely fit dosage. The need for these can change from day to day, depending on the warmth of the weather, or how stressful you are. To reduce possible side effects it is advised that you don't take more than 6 a day, and leave a 4 hour gap between each dose. These might increase the production of saliva glands in certain patients who have complaints about swallowing and chewing; and also nausea, vomiting and diarrhea in some. Even though I never encountered any of these, one should be careful not to overdose.

Thymectomy
The surgically removal of the thymus gland is advised to most Myasthenia Gravis patients. The surgery doesn't show considerable improvement in patients over 60, and take about 2 to 5 years to show its effect on others. In 2006, an international coalition has been started to completely discover thymectomy's effect on the disease. Thymectomy has two methods which can simply be called open and closed. The open method can be difficult and painful, as it requires the whole chest area to be cut open, and it can take a long time to be released from the hospital. However, the closed method is much easier on the patient, I was released on my second after the surgery, and went abroad to a summer camp just three weeks later. If you are going to have the surgery with the open method, you should enquire how long you will have to stay in the hospital and how long it will take you to get better carefully.

Corticosteroids (Cortisones)
Corticosteroids considerably decrease or completely clear the symptoms in 75% of the patients, and create some improvement in the rest. Most of the improvement takes place in the first 6-8 weeks, and complete healing may take place in the successive months. The best results are received with patients who have severe symptoms before the drug use. Once you have started using these drugs, you should never quit them without discussing it with your doctor carefully, the best is to keep using them for a long time in very low doses before you completely quit them. I once managed to convince my doctor in totally quitting them, however it was only 1.5 months before the symptoms came back. It is also possible for the symptoms to slightly worsen in the first 7-10 days of the use of these drugs. The worst part of corticosteroids are their inevitable adverse effects; although techniques such as starting in low doses and increasing the dosage slowly can be used to decrease them, I suggest you keep your morals high and prepare yourself for the worst. Once you start using them, you must completely erase salt from your diet, because salt is one of the main reasons you gain weight while on corticosteroids. Weight gain might also cause stretch marks on your body. There are many things to say about corticosteroids; when I was using them on high doses I was almost more demoralized by the adverse effects rather than Myasthenia Gravis. You should prepare for your appetite to increase twice as much, and decrease sweets if you like them before you even start using the drugs, and prefer a vegetable based diet. Stretch marks can be a real cause of annoyance especially in girls and women, as it was in me, I admit I did not want to wear short sleeves or skirts for a long time. I have tried many skin products and I can say that the only thing that gave me a visible result was the mousse version of OHT Peptide3. It's not the cheapest one out there, but it was the only one I found effective. Some types of corticosteroids bring the risk of cataract with them, the best is to visit your eye doctor regularly once a year or even siz months. Cataract (or the beginnings of it) usually disappear once you decrease the cortison dosage.

Immunosuppresants
I do not have too much information on these drugs right now, how are this category includes the ones known as CellCept and Imuran. The biggest drawback of these is that they can not be used during pregnancy. I shall update this section as I gather more info.

Plasma Exchange (Plasmapheresis)
This is a short term solution for patients who suffer from a sudden worsening of symptoms for any reason, patients who do not respond to other treatment may use this periodically. The need and frequency of plasmapheresis change depending on each patient's condition. Although improvement might last for weeks or even for months, it does not have a lasting effect unless combined with thymectomy or corticosteroids. There's nothing special I can say about it as I have not tried it myself.

Intravenous Immune Globulin (IVIG)
Although it is unknown why this method works, it creates improvement in most patients about a week after it is done, and the effect lasts between 2 weeks to 3 months. It is usually given to patients between 2 to 5 days. The drug's side effects depend on the rate of application, and though some of them might sound scary, they are temporary. To give a list; headache, dermititis (inflammation especially in soles and palms), pulmonary oedema (fluid in the lungs), allergic reactions, hepatitis (inflammation of the liver), acute renal (kindey) failure, blood clotting, aseptic meningitis, vomiting. The only side effects I ever encountered were inflammation in my fingers and vomiting, which are insignificant compared to the relief it brings. However, I never took it in less than 5 days, so I can not comment on the side effects you will feel if you take it in less than 2 days. It also does take some getting used to the serum tied up to your arm, it is my experience that the drug moves faster if you manage to never move your arm.