What is the best treatment for multiple sclerosis.?
Answer:
It really depends on the lenient and how he/she is affected by the MS and the treatment. That is, the best treatment for me, might not be the best treatment for you.
As someone else own mentioned tysabri is mostly prescribed when the other drugs are unsuitable for one reason or another - or if your MS is outstandingly aggressive.
Each drug has its advantages or disadvantages. The best would be to hold a talk beside your neurologist about it and study the medication on their respective home page. Your neurologist can inform you about the meds., and aid you find the ones that would be best suited to you, and you can then dogmatic down the options by taking your lifestyle and nature into consideration (do you travel often? How do you be aware of about each day injections, every second day or weekly injections? Would you prefer to inject lower than the skin or into the muscle? How about going to hospital once a month for treatment? etc.)
Once you enjoy chosen the treatment, it need not be a life-long commitment. Usually the first months - 1 year are more close to a trial period to see how all right you, your body and the MS reacts to the medication.
Have you thought nearly trying alternative treatments? My mother had MS for years and we tried the treatments they have available at the time (1980's). I remember her going into the hospital for ACTH treatments and then another treatment that we use to inject within her backside (but I don't remember the name of it). Neither did anything to increase her condition. Then we decided to try an alternative treatment. I know it sounds strange but we tried bee stinging therapy (another heading for it is Apitherapy). Interestingly enough it help more than any other treatment had. She regain some of her function that she had lost years earlier. Anyhow, I wish you the best of luck and hope you find a treatment that help you.
Various disease-modifying treatments have be approved by the USA's Food and Drug Administration (FDA); as well as contained by other countries; for multiple sclerosis.
INTERFERONs:
These are medications derived from human cytokines which support regulate the immune system. Betaseron has be approved by the FDA for relapsing forms of secondary progressive MS.
Interferon beta-1a: (trade name Avonex , Rebif and CinnoVex [Biogereric/biosimolar form of Avonex])
beta-1b: (trade name Betaseron [in Europe and Japan Betaferon]).
GLATIRAMER ACETATE: (trade identify Copaxone)
A synthetic medication made of four amino acids that are found in myelin. This drug stimulates T cell in the body's immune system to translation from harmful, pro-inflammatory agents to beneficial, anti-inflammatory agents that work to cut back inflammation at lesion sites.
MITOXANTRONE: (trade name Novantrone)
This medication is impressive, but is limited by cardiac toxicity. Novantrone have been approved by the USA's FDA for minor progressive, progressive-relapsing, and worsening relapsing-remitting MS.
NATALIZUMAB: (trade name Tysabri).
This medication is efficient and safe alone but within combination with other immunotherapies can front to PML.
Tysabri is NOT a first line of treatment for MS b/c it is associated next to the risk of PML which can be fatal. It is one and only prescribed for people who former other meds for MS. The purpose of MS drugs is to keep the MS from progressing to the point where on earth it is disabling. Several options are: Avonex, Betaseron, Copaxone, Rebif. The National MS society have a GREAT website. I use Betaseron which is injected every two days - you'll get used to it. No oral drugs all the same but should come out in the subsequent couple of years. Good luck.
try chemo
My son was diagnosed near MS 3 years ago and has be on Avonex. It is an injection that goes open into the muscle, but is only given once a week. SInce individual on Avonex, he has have no major problems beside his MS. He is looking forward to the day of oral medication.
Your neuro should know which one to try first. My understanding is that Tysabri is a end line defense. People can notify you what they use and what it has done for them or what reaction they have have, but you know this disease looks different on each individual so that really doesn't help YOU!! Talk to the neuro and do what he/she recommend. Do your research go to NMSS and MS foundation sites, as capably as the medicine sites - I know rebif have one - I've been near - Just Google the drug name.
Good luck!
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