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Which advice would you give to someone who has just been diagnosed with Multiple Sclerosis?

See some advice from people with experience in Multiple Sclerosis to people who have just been diagnosed with Multiple Sclerosis

Multiple Sclerosis advice
13 answers
Translated from spanish Improve translation
He continues his life as until now, with some inpedidento, but, to continue forward..be strong

Posted Feb 28, 2017 by Belén 1111
Translated from spanish Improve translation
THE MOST IMPORTANT, THAT YOU START WITH YOUR MEDICAL TREATMENT, IF YOU WANT TO SEE OTHER OPTIONS SUCH AS ALTERNATIVE MEDICINE, ACUPUNCTURE, NATUROPATHY, ETC. TO DO SO, BUT NEVER STOP YOURSELF, HAVE A POSITIVE ATTITUDE TOWARDS LIFE, THAT THIS IS NOT JUST WITH MS, THAT YOU CAN LEAD A GOOD LIFE, THAT IS NOT THE END OF THE WORLD, THAT THERE IS A STRUGGLE DAILY AND NOT TO BE OVERCOME.

Posted Mar 1, 2017 by Jose 1140
Translated from spanish Improve translation
Do not be afraid.
Enjoy every sunrise.
Enjoy your life to the fullest.
You make it all up to where your body will allow.

Posted May 4, 2017 by Antonio 1050
Translated from spanish Improve translation
Life does not end with this disease, we have to fight this life, some more than others, and while they accept the new companion with a good attitude will not affect your life, be attached to the treatment

Posted May 4, 2017 by Bely 1000
Translated from portuguese Improve translation
The diagnosis is a both scary and seeking knowledge on the Internet is a double-edged sword.
The ideal is to seek information from your doctor, and talk with people already diagnosed and the help of a Psychologist to the patient will help you experience a milder form of this new step.

Posted May 11, 2017 by Thais Sivieri Tauil 1000
Translated from portuguese Improve translation
Calm FAITH and strength today we have many resources treatments.

Posted May 11, 2017 by Tatiane 1000
Translated from portuguese Improve translation
Defines your priorities.

Posted May 13, 2017 by Rui Rodrigues 2650
Translated from spanish Improve translation
That is a disease that has no cure, but that is being researched and will soon reach the answer that we all hope for.

Posted May 31, 2017 by Laura 2000
Translated from spanish Improve translation
A person newly diagnosed in the first place, deb, take a breath and accept the reality in a positive way. Immediately go where your neurologist to this to explain and to clarify their doubts about his condition. The patient should be put attention to the treatment chosen by your neurologist in order to avoid complications with the condition and stay stable

Posted Jun 1, 2017 by Ezequiel 2100
Translated from french Improve translation
Contact an association

Posted Aug 16, 2017 by johnny 1000
Translated from french Improve translation
attention has the power, keep your faith in the future and enjoy every moment

Posted Aug 16, 2017 by Boucheron 1125
Translated from french Improve translation
Continue to live without worrying about it. Of course, to be limited according to its strengths and its difficulties, but life doesn't change!

Posted Oct 2, 2017 by Joseph Alaimo 1000
Translated from portuguese Improve translation
With calm life goes on

Posted Oct 6, 2017 by Maria Manuela 1020

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I would like to know if extreme fatige and muscular weakness can be early symptoms of multiple sclerosis. Should I take more tests to discard ms or these symptoms are not ms symptoms?
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Has anyone had an elastofibroma removed? I have two large ones that need to be removed and would ike to know about post surgery and recovery.

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