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ALS MS in focus 14, Spanish version

is now available on the web to download the magazine number 14 MS in focus, published by the MSIF (Multiple Sclerosis International Federation).

IMAGE: home MS in focus number 14

can
the PDF file and refer to electronic mode or print on paper and share it with those who do not have access to the Internet.

printing editing MS in focus circulates only in English, and is delivered by mail throughout the world, but the electronic version when produced in different languages.

At the last meeting and workshop of the International Committee People with MS who had in Chicago on October 31, we request you consider printing the magazine in English and is mailed to English-speaking countries.

In Latin America need to know more about multiple sclerosis and MS in focus is a major effort by the MSIF to make this possible.

at number 14, devoted to the types of multiple sclerosis, you will find:

• Introduction to the types of MS disease
• relapsing-remitting MS
• primary progressive MS
• progressive MS secondary
• Extreme cases of MS: benign and aggressive forms
• clinically isolated syndrome
• Answers
• Poll Results
• Help for people newly diagnosed
• Interview with James West

-------------------- English
The number of MS in focus 14 , the disease courses in MS, is now available. Click here to download the file: http://www.msif.org/es/publications/ms_in_focus/index.html

The contents of MS in focus is based on the knowledge and experience. The publisher and authors are striving to provide current and relevant. Maybe the opinions and ideas expressed do not match those of the MSIF. The information provided by MS in focus is not intended to substitute for the advice, prescriptions or recommendations from doctors or other health care. For specific information and personalized, consult your health care service. MSIF does not approve, endorse or recommend any specific product or service, but provides information to help people take their own decisions.

The next issue of MS in focus will be on complementary and alternative therapies for MS.

Back issues are available printed or downloaded from the website of MSIF.

• No. 1 How to combat fatigue
• No. 2 Special: How to combat bladder problems
• No. 3 edition devoted to the family
• No. 4 Aspects emotional and cognitive
• No. 5 Healthy Living
• No. 6 Intimacy and Sexuality
• No. 7 Rehabilitation
• No. 8 Genetics and inheritance of MS
• No. 9 EM and care
• No. 10 Pain and MS
• No. 11 Stem cells and Remyelination in MS
• No. 12 Spasticity in MS
• No. 13 Tremor and ataxia in MS

Hope you like the magazine

MVZ Hector M. García Caballero

Executive Committee Member and Representative of Mexico to the International Committee
of People with Multiple Sclerosis (PwMSIC / MSIF) Multiple Sclerosis International Federation

@: drhectorgc@gmail.com

Shoulder Pain After Laproscopic

Redefining the course of multiple sclerosis

I asked a person he few hours, what's new in the treatment of multiple sclerosis.

And just want to publish an invitation to a symposium to discuss developments in treatment, and importance of adhering to medical indications.

IMAGE: Zoe invitation for the sake of symposium "Redefining the course of MS."

On Saturday November 28, 2009, the Hotel María Isabel Sheraton (Paseo de la Reforma 325, Col. Cuauhtémoc, Mexico City) will be held the symposium "Redefining the Course of Multiple Sclerosis" .

is an open event at no cost, only need to confirm attendance.

And for those who wish to attend from Cuernavaca, the organizer shall provide transportation for our association FOR LOVE ZOE.

The lectures will be conducted by specialists Carlos Cuevas Garcia, chief of Neurology, Hospital de Especialidades, National Medical Center "Siglo XXI", José de Jesús Flores Rivera, the Multiple Sclerosis Clinic of the National Institute Neurology and Neurosurgery, and Leonardo López Llamas, Neurology Service the ISSSTE Guadalajara, Jalisco.

The event, organized by Stendhal Symposia, lasts all day: the first part are presentations at medical and question and answer session.

IMAGE: Agenda of 28 November 2009, Symposia programmed by Stendhal.

then offered a box lunch to the attendees, and the afternoon will be two workshops: one on nutrition and the second called "laughter yoga."

"Laughter Yoga" is a workshop facilitated by a person with MS, Karla Oseguera, who has worked this activity in previous symposia in Zacatecas, Guadalajara and Campeche.

We will be happy to find there friends and family members, caregivers.

But ... What's new for
treat multiple sclerosis?

I think it's a common question in those who live with MS or who are close to us.

I have also received messages with the doubt if I know someone-data in the world has recovered from multiple sclerosis.

PHOTO: Questions and answers on the Third National Multiple Sclerosis 2008.

And no, I know someone who reliably been removed from your body all symptoms caused by MS, although there may be remyelination or reverse some damage but that it disappeared and multiple sclerosis, no.

Questions like: What could I have done that provoked me MS? Have I been a warning I ignored? Could I have prevented it? "I do not care enough? And a long list of questions my thoughts were about the early years of the disease, but the most pressing concern was that I be able to recover?

When my diagnosis in 1989-after six years after the first outbreak had sent me one month to the hospital, there were no specific drugs to treat multiple sclerosis, and then in the 90s to get to Mexico Interferon Beta, expectations were almost sensed it was not really secure the future.

The boom beta interferon

In the 90's, through patient associations (there were many) was sought "to encourage "people to accept or request the application of interferon in treatment.

And told me a doctor who was diagnosed nearly 30 years ago, he could have chosen to inject interferon beta, but decided against it.

PHOTO: Patients, family members, caregivers and health professionals at a conference.

More than 15 years later, this person, whose only sequel obvious is the need to use a cane to walk, agreed to try the treatment, but ... He believes that the side effects were much more annoying than the overall state where he has lived all these years. Decided to discontinue the injections after one month trial.

Cases like this have read and heard many: people who stop or not followed to the letter, or simply do not believe in it, people may have periods of stability or improvement temporary and believe that drugs would not have done differently during the course of the disease.

I differ on these findings, and instead-or overestimated appreciate being informed of the medications available to treat multiple sclerosis.

Why have I taken pharmacology!

I am interested because I want to know what I'm putting in my body, which is expected to do in my body, how long and with what chances of success.

professional bias may seem (I get natural terms like "dose" or "pharmacopoeia" and "pharmacokinetics"), but in the end but did not use such long words, the point is that I know everything about medicines can help my condition.

PHOTO: Commercial Exhibition Area at the Fourth National Multiple Sclerosis 2009.

And if a new product on the market, even if it is not recommended in my personal condition, secondary progressive MS with 26 years of evolution, "I know all the information.

the pharmaceutical and medical marketers, know this, and people with multiple sclerosis, we facilitate learning: it is common to receive invitations to breakfasts, lectures, presentations as specialized neurologists and / or researchers answer our questions related to MS and its treatments.

is valuable for people with MS receive this information, learn and build knowledge.

Scientific Research and the pharmaceutical industry

One of the global efforts in the fight against MS is to promote medical research and work tirelessly to find the cause etiologic and cure, but in that interval that science requires, must obviously improved therapeutic options.

IMAGE: Cartel "Redefining the course of MS."

The Multiple Sclerosis International Federation (MSIF), whose international committee of people with MS I am part, has programs and activities designed to promote, monitor and disseminate research advances and protocols related to multiple sclerosis.

care that requires a person with MS is integral, physical rehabilitation, psychological support, nutrition, behavior change and adaptation of activities, but the quality of life is to combine all that with specialized medical treatment. The neurological consultation and medication (pharmaceutical) indicated to treat multiple sclerosis, have shown positive results provide a better life expectancy.

The transnational corporations involved in drugs, investing millions in developing specific drugs for multiple sclerosis, and in 20 years we have seen the growth of a range of options that began with the onset of interferon beta.

followed Glatiramer acetate, whose use has spread and become popular in many countries, but now there are new and better? alternatives for Neurologists doctors prescribe to their patients.

And while the Beta Interferon and Glatiramer Acetate have shown effectiveness in a 30 percent relapse, monoclonal antibodies, which have passed testing and approval in several countries reported 68 percent reduction of relapses.

PHOTO: rehabilitation workshop during the National Meeting in Puebla.

Data cold statistics result can mean something to some people, others may not say anything or even feel like they know these figures,

but ...

if these comments and explains the points directly to a specialist who has experience treating patients with credits in the area of \u200b\u200bmultiple sclerosis, and having investigated the matter, the result is definitely more useful.

have access to first hand information and state our concerns, which does not express time-consultation, get answers and learn about our disease, it is always good.

What Does Pierced Nipple Mean?

IV National Multiple Sclerosis Meeting 2009

Piece of heaven Earth

Puebla ... that's my pretty ...
... this is my holy land ...

Angels Heavenly streets laid out the city of Puebla, the legend.

PHOTO: Catedral de Puebla de los Angeles

With masterly design of wide, straight roads orientated North to South and East to west, just "as God commands," was drawn level ago almost 500 years. Ethereal strings attached by hand became the winged messengers surveyors working.

But the perfect design of the streets Puebla is not everything, "Dona Maria", the bell of the Cathedral, said to have been uploaded to the very high domes since 1732 angels and chimes in top of the temple.

Of the divine presence is that the fair was named Puebla de los Angeles .

PHOTO: Presidente Intercontinental, headquarters of the IV National Multiple Sclerosis Meeting

Also known as "Angelópolis" this capital located just over one hour from Mexico City will host the Fourth Meeting National Multiple Sclerosis "in Puebla, hand in hand", from 2 to 4 October 2009.

A gathering of friends

During the first weekend of October at the Presidente Intercontinental hotel, we met people with multiple sclerosis (MS), family, friends, caregivers, volunteers, nurses and physicians to share and learn more about what it means to live with MS.

PHOTO: Talavera

From Friday at noon is expected to start arriving people from all over Mexico, and even some other countries, for this fraternal meeting and learning that 2009 corresponded to organize the Multiple Sclerosis Association Puebla de los Angeles (EMPA).

MS Puebla de los Angeles

diligently led by Mave Hernandez, Rosie's sister and caregiver, which has MS for 30 years, clustering EMPA is credited a good resume service and support to people with MS in the state of Puebla and surrounding cities.

As part of the federation Multiple Sclerosis Mexico AC (EMMEX), which groups the civilian relief organizations in MS cases across the country, the association president Mave was elected to be responsible for organizing in your town the Fourth National Meeting.

PHOTO: Pool at the Hotel Presidente Intercontinental Puebla

Under the motto "In town, next to the Hand" extends the invitation to anyone interested in listening to lectures, participate in workshops and live for Friday, Saturday and Sunday, in which specialists neurologists, psychologists, physiotherapists, ophthalmologists and otolaryngologists, will discuss implications and treatment of MS in their areas of expertise.

from all of Mexico, is expected to hundreds of attendees

The Fourth Meeting of Multiple Sclerosis, directed basically to people with MS is part of the efforts made in Mexico EMMEX to promote a better quality of life.

first home in 2006 This traditional gathering of multiple sclerosis was the colonial city of Zacatecas to the north of the country, and then in 2007 came together in central Mexico in Mexico City, capital of the nation, and last year, 2008 The venue was the "Pearl of the West" Guadalajara, the birthplace of mariachi and tequila.

PHOTO: typical dishes from Puebla kitchen

But 2009 promises to be a unforgettable experience Puebla, located east of the Federal District, is one of the 32 states of Mexico, and has distinguished itself as a region rich in history, tradition and distinguished cuisine.

The capital, Puebla de los Angeles-host the Fourth Meeting, has a beautiful historic center and has been declared a World Heritage Site.

coexistence activities

On the social side of the work program of the Fourth National Multiple Sclerosis Meeting included a tour Optional Puebla attractive sites.

For an additional payment to the registration, you can visit places that their identity and style characteristics were chosen as the scene of the movie "Arráncame Life , based on the work of writer Angeles Mastretta Puebla, which portrays in his novel Life of Catherine, played by Ana Claudia Talancon beautiful-in the traditional patriarchal society of Puebla in 1930.

PHOTO: Hotel Holiday Inn Express Puebla

And if you want to explore the corners of Puebla in a more spontaneous, have a couple of hours in the afternoon / evening of Saturday, or Sunday morning, before handing hotel room one in the afternoon, to hear the host city.

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Put Pokemon On Blackberry

What we say

so clear and so true, in our hands to build and strengthen self-esteem of our children, but not just about tell you how much we love him, but also demonstrated by our actions.

That which we
Laura Gutman - Newsletter September 2009

Children believe in parents. When I say over and over that they are sorcerers, who are the princes and princesses of the house, are handsome, smart, intelligent and funny, become that which we say they are. By contrast, when we tell them they are fools, liars, bad, selfish or distracted, obviously responding to the mandates and act as such. That, or parents who take care of raising- say, constitutes the most solid child's identity.

Children have more virtues than others. However, the child looked insufficiently , pampered, and taken into account bespoken by their parents, give greater credence to their disabilities. And suffer. Instead, the child looked at and admired by his parents, loved by loving acts everyday, will have a self-confidence that will allow erected on its greatest virtues and laugh while their difficulties.

If we realize that our children suffer, if they have low self-esteem if they are ashamed, if you feel bad athletes, poor students, or do not fall short of the circumstances, if they can not talk, socialize, play with others, if assumed to be slow, or are victims of ridicule from their peers, for us to drive for them right now . The worst thing we could do is required to bear alone problems.

We can name those virtues, resources or skills that child does have as an individual. For example, a child who always tells the truth. That would never betray a friend. That is incapable of hurting another. He observes and understands the suffering. That is generous and tolerant. Tell the children that are beautiful, loved, welcomed, adored, noble, beautiful, who are the light of our eyes and the joy of our heart and generates children safe, happy and wise. It is possible that the pretty words do not appear in our vocabulary, because we have never heard in our childhood . In that case, we have to learn. If we do this work now, our children, to become parents, will not have to take this lesson. Arise because of his heart quite naturally, the most beautiful words and phrases most rewarding for their children. And these strings of words of love be perpetuated for generations, without which our grandchildren and great repair them because they will make part of their way to be genuine. Consider it an investment in the future with zero risk. From now on ... just words of love for our children! Yell to the wind that we love to heaven. And higher still. And more and more.

Extract from an article book Women visible, invisible mothers "by Laura Gutman

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