Thursday, September 23, 2010
How Much Is Ptosis Repair
Come to Monterrey. Go ahead, relative!
"Today more than ever, we value life
"... The Hurricane (Alex) left us soaked and broken streets. The good thing is past and the kicker ... In Monterrey, more than ever we value life. " Thus ended one of the emails sent Roxana González Cáceres (pictured left, Roxana appears carrying his nephew) during the months of preparation the 5 th National Congress of MS.
Roxana is a woman always smiling, positive, enthusiastic, intelligent and certainly a very unique charm, but now that he has had to organize the event largest Mexican family with amyotrophic Multi-our annual meeting, "added a quality to his personality, the brave.
Roxana is a brave woman, not even deterred by a hurricane or faint while planning the National Congress. was getting donations, reviewed the venues, negotiating the best services and not a day longer encourage us to participate in this great meeting.
Alex was the first hurricane of the 2010 season, and damaged some parts of Mexico, in the Northeast fell to Monterrey on July 1, but although as well-broke Roxana said some streets could not break anything in the spirit of the Regiomontana Association of Multiple Sclerosis (ASREM) ABP which had already been several months preparing for the Congress.
ASREM, an organization chaired by Roxana, is the association representing Monterrey people living with multiple sclerosis (MS).
Founded in 1994, belongs to the federation ASREM MS Mexico EMMEX AC * and performs various activities in your area to support people with MS.
Dr. Cesar Lozano, for example, better known now for his appearances on the television program NOW offered a conference to support the fundraising ASREM and thus the association may be offering more and better aid. And so have had several fundraising events and service activities. ASREM
medication assistance, efforts and financial support services to people with MS in Monterrey. It is a private charitable organization, regulated and authorized tax deductible receipts to issue to their benefactors, thanks to those who achieve better results.
now ASREM shines with the National Congress
Excellently organized, 5 th National Congress of EM (for detailed information, to click on the underlined name) promises great experiences: the conference program is extensive and intensive activity is uplifting and fun Sunday, and Saturday night will be an elegant dinner dance.
As if that were not enough, we have prepared several surprises: you will be living with Congress attendees Mexican actress Silvia Pasquel, who has a long history in theater, film and television. Daughter of the famous Silvia Pinal national movie star, Silvia Pasquel, currently residing in Monterrey, gladly accepted the invitation.
The also b ien Mexican actress Alejandra Maldonado, mainly career in soap operas, attending her as a patient who received sometime b ed the diagnosis of multiple sclerosis.
The presence of these two women adorn the weekend, but also b b ien has Ra a highly valued for its content, was published especially for the day li b ro "The Lord of the b ugamilias" sense beautiful testimony of a man b who lived his last re years with amyotrophic lateral sclerosis (ALS) and shares in li b ro an intense love for life and an emotional charm things b them from nature.
amyotrophic lateral sclerosis (ALS), also disease b ien incurable b le, but this other mortal, unlike multiple sclerosis does not cause death, "shares the nom b re" sclerosis "but is actually a very different disease to MS, different course and treatment, but certainly those with either reflected in the other share many similarities and moods.
and therefore may be less frequent ALS to find, many people with ALS are close associations with MS and are to ren b spaces for activities they wish to join.
Currently, much of Mexico, the MS societies have among its members b ros people with ALS. And in particular our partnership Morelos ZOE MS is trying to form a network of people with ALS -communication that can keep them or their family members through e-mails or phone calls to share their experience.
The proposed link for people with ALS is contacting Faivel Polichuk, ZOE counselor who has ALS and is determined to achieve this network. You may www.faivelpolichuk.net contact from the site.
pharmaceutical companies producing or distributing specific drugs to treat MS are the main sponsors of the event, whose contributions it was possible that large numbers of people traveled snipe and prices for those who pay their attendance are usually minor. 
The city of Monterrey, the most northern Mexico, capital of the prosperous state of Nuevo León, opens its doors from 24 to 26 September 2010 the community Multiple sclerosis (MS) to celebrate the 5 th National Congress of Multiple Sclerosis at the Camino Real. And there we go!
"Today more than ever, we value life
By Ana Silvia Barajas and Hector Garcia Garcia Knight
PHOTOS: Images of Monterrey and several host hotel
"... The Hurricane (Alex) left us soaked and broken streets. The good thing is past and the kicker ... In Monterrey, more than ever we value life. " Thus ended one of the emails sent Roxana González Cáceres (pictured left, Roxana appears carrying his nephew) during the months of preparation the 5 th National Congress of MS. Roxana is a woman always smiling, positive, enthusiastic, intelligent and certainly a very unique charm, but now that he has had to organize the event largest Mexican family with amyotrophic Multi-our annual meeting, "added a quality to his personality, the brave.
Roxana is a brave woman, not even deterred by a hurricane or faint while planning the National Congress. was getting donations, reviewed the venues, negotiating the best services and not a day longer encourage us to participate in this great meeting.
Alex was the first hurricane of the 2010 season, and damaged some parts of Mexico, in the Northeast fell to Monterrey on July 1, but although as well-broke Roxana said some streets could not break anything in the spirit of the Regiomontana Association of Multiple Sclerosis (ASREM) ABP which had already been several months preparing for the Congress.
ASREM, an organization chaired by Roxana, is the association representing Monterrey people living with multiple sclerosis (MS).
Founded in 1994, belongs to the federation ASREM MS Mexico EMMEX AC * and performs various activities in your area to support people with MS.
Dr. Cesar Lozano, for example, better known now for his appearances on the television program NOW offered a conference to support the fundraising ASREM and thus the association may be offering more and better aid. And so have had several fundraising events and service activities. ASREM
medication assistance, efforts and financial support services to people with MS in Monterrey. It is a private charitable organization, regulated and authorized tax deductible receipts to issue to their benefactors, thanks to those who achieve better results.
now ASREM shines with the National Congress
Excellently organized, 5 th National Congress of EM (for detailed information, to click on the underlined name) promises great experiences: the conference program is extensive and intensive activity is uplifting and fun Sunday, and Saturday night will be an elegant dinner dance. nice surprise
The also b ien Mexican actress Alejandra Maldonado, mainly career in soap operas, attending her as a patient who received sometime b ed the diagnosis of multiple sclerosis.
The presence of these two women adorn the weekend, but also b b ien has Ra a highly valued for its content, was published especially for the day li b ro "The Lord of the b ugamilias" sense beautiful testimony of a man b who lived his last re years with amyotrophic lateral sclerosis (ALS) and shares in li b ro an intense love for life and an emotional charm things b them from nature.
amyotrophic lateral sclerosis (ALS), also disease b ien incurable b le, but this other mortal, unlike multiple sclerosis does not cause death, "shares the nom b re" sclerosis "but is actually a very different disease to MS, different course and treatment, but certainly those with either reflected in the other share many similarities and moods.
and therefore may be less frequent ALS to find, many people with ALS are close associations with MS and are to ren b spaces for activities they wish to join.
Currently, much of Mexico, the MS societies have among its members b ros people with ALS. And in particular our partnership Morelos ZOE MS is trying to form a network of people with ALS -communication that can keep them or their family members through e-mails or phone calls to share their experience.
The proposed link for people with ALS is contacting Faivel Polichuk, ZOE counselor who has ALS and is determined to achieve this network. You may www.faivelpolichuk.net contact from the site.
sponsorship, the key to success in Monterrey
pharmaceutical companies producing or distributing specific drugs to treat MS are the main sponsors of the event, whose contributions it was possible that large numbers of people traveled snipe and prices for those who pay their attendance are usually minor.
Stendhal
Neuroscience, Bayer de Mexico, Teva, Pisa, Merck Probiomed and awarded scholarships to members of associations belonging to special cases EMMEX and others independently, with funding from the laboratories there may be additional assistance.
official sector also made significant contributions. Directly to the City of Monterrey, the state government of Nuevo León, the tourist office of Nuevo Leon, the convention area and the hotel Camino Real, host the meeting, pledged to the project and contributed generously.
Professional Convention The company is taking care of logistics and general Congress has been from the beginning a high quality event.
In anticipation, people with MS, caregivers, family, nurses, therapists, medical representatives and other professionals related to the concept of "living with MS," began arriving in the North called Sultana, road and air.
Wednesday evening made the trip from Mexico City United fellow Fighting Multiple Sclerosis (SSMU) is the newest association EMMEX *. Around midnight, headed by Lucifer, the president, members of SSMU and were near Querétaro, with very good spirits and very spoiled by Lupita Cruz, charged at the national level of patient care by Bayer Health Care . Lupita
addressed personally to the bus of all passengers take UCEM a snack to hold the 12-hour trip. And on Thursday to do so in association rented bus EMAC DF in which patients and their companions travel from Toluca, Cuernavaca and Mexico City.
in western Mexico, traveling by road-organized by Ninfa Monarres-members of the MS Society of Jalisco and the Fegolo of Irapuato, Guanajuato.
From Puebla, Mave Hernández is an enthusiastic group. Saltillo, Coahuila META association also has a nice group, and each corner to join in our annual festival. Some delegations
with fewer or more numerous, but we will all be present on this occasion that allows us to learn, rediscover friends and spend pleasant moments together as a community.
logistical support
To facilitate the transfer of those arriving by plane Monterrey transportation will be available at the airport in 12 to 15 hours on the door b. The bus will send the UR Association at no cost to the passengers to the Hotel Camino Real.
all accessible to people with disabilities
The Camino Real Monterrey Gran Turismo is a new resort with has b itaciones comfortable and each shower services suitable for people with pro b slogans mobility.
Camino Real staff has worked hard in preparation Congress. Special menus were designed for the occasion, there will be several rooms for different activities and is generally all that we calculated for maximum comfort.
Neuroscience, Bayer de Mexico, Teva, Pisa, Merck Probiomed and awarded scholarships to members of associations belonging to special cases EMMEX and others independently, with funding from the laboratories there may be additional assistance.
official sector also made significant contributions. Directly to the City of Monterrey, the state government of Nuevo León, the tourist office of Nuevo Leon, the convention area and the hotel Camino Real, host the meeting, pledged to the project and contributed generously.
Professional Convention The company is taking care of logistics and general Congress has been from the beginning a high quality event.
The crossing
Wednesday evening made the trip from Mexico City United fellow Fighting Multiple Sclerosis (SSMU) is the newest association EMMEX *. Around midnight, headed by Lucifer, the president, members of SSMU and were near Querétaro, with very good spirits and very spoiled by Lupita Cruz, charged at the national level of patient care by Bayer Health Care . Lupita
addressed personally to the bus of all passengers take UCEM a snack to hold the 12-hour trip. And on Thursday to do so in association rented bus EMAC DF in which patients and their companions travel from Toluca, Cuernavaca and Mexico City.
in western Mexico, traveling by road-organized by Ninfa Monarres-members of the MS Society of Jalisco and the Fegolo of Irapuato, Guanajuato.
From Puebla, Mave Hernández is an enthusiastic group. Saltillo, Coahuila META association also has a nice group, and each corner to join in our annual festival. Some delegations
with fewer or more numerous, but we will all be present on this occasion that allows us to learn, rediscover friends and spend pleasant moments together as a community.
logistical support
To facilitate the transfer of those arriving by plane Monterrey transportation will be available at the airport in 12 to 15 hours on the door b. The bus will send the UR Association at no cost to the passengers to the Hotel Camino Real.
More so ber Congress Multiple Sclerosis
information pricing is available b you on page we b www.ilovemty.com.
all accessible to people with disabilities
The Camino Real Monterrey Gran Turismo is a new resort with has b itaciones comfortable and each shower services suitable for people with pro b slogans mobility.
Camino Real staff has worked hard in preparation Congress. Special menus were designed for the occasion, there will be several rooms for different activities and is generally all that we calculated for maximum comfort. On the ground b aja hotel stands will be the section of pharmaceutical companies and another area has b ela Ra selling products b orated by the various member associations b EMMEX Ros.
Even today Thursday and Friday morning after an activity is performed independently: Karla Oseguera, a person with MS who has spent recent years to provide speech and language workshops laughter yoga, called for those wishing to become certified as facilitators of laughter yoga to take a crash course in the same seat in Congress.
EMMEX * AC is the umbrella organization for associations with multiple sclerosis of the Republic b lica Mexicana. You can search the directory of associations in the b log http://emmex-ac.blogspot.com
Gallery ...
Tuesday, September 14, 2010
2005 Pilot Front Plate
In memory of my friend Manuel
My friend Manuel Meneses died Monday September 13, 2010.
In the photo-taken in Leon, Guanajuato, in May 2009 - appears with his wife Ninfa.
his absence hurts but I know that his spiritual progress continues, its existence is not limited to this world, but continues, and knowing I will achieve significant progress in their personal progress.
pray that their families and those we miss, when we receive comfort from our Lord.
command a special greeting to his widow Monarres Ninfa, my friend and inspiration to help others.
Manuel was a very special man, happy and jovial, a lover of life and excellent host. He suffered from Parkinson's disease for several years but that never prevented him from enjoying the sun and food, exercise and share with people.
in October 2009 gave us a lesson in what are truly feel like dancing when you put down your walker to follow the rhythm of the music with his beautiful wife.
Manuel was a master of life, retired from the armed forces of the United States, their physical strength will always beat the disease and even the delicate surgeries that were performed.
Modesto and cordial, showed his experience as a swimmer and even shared his lessons with my son Mariano, while they were swimming together in Toluca, just over 2 years.
Mariano called him "my friend" and both are seeking to enter the pool or to raid the breakfast buffet. And Manuel walking with his walker or, as in the last year on his motorized wheelchair, Mariano wondered whenever we saw.
never forget the day I met Manuel, in 2007. He came driving to Cuernavaca. Ninfa only lowered the car and he said he would wait outside, but decided to join us. We sat under an orange tree in the garden and an impromptu lunch "turkey" (tamale pie) while Mariano was splashing around in the wading pool. And from that moment I could see in his face and the smile of Manuel that he was a man who would be worth learning.
Today is no longer with us but I know that someday return to eat a "turkey."
On that occasion, as always, Manuel went with her husband and supported. Proudly enjoyed international recognition that his wife was in Chicago, USA.
Like every time we met, Manuel was happy and friendly.
PHOTO: with Talpa Manuel Gonzalez, president of the Foundation Fegolo, Irapuato, Guanajuato.
COMMENTS:
Dear Hector,
I just heard the sad news through this newsletter that you send me and I have been shocked.
remember so close to Manuel, in Guadalajara and the last time in Chicago ... always with his beloved nymph, helping all he could despite his limitations.
My most sincere condolences to the family of Mexican MS. A hug
Pedro Carrascal
Executive Director of the English Federation to Fight Multiple Sclerosis
September 14, 2010 15:56 hrs.
Thanks --- Hector:
Stories like yours and we have narrated in memory of Manuel, feed the soul and strengthen the spirit.
already Bertolt Brecht said: There are men who fight one day and are good, but there are men who struggle all their lives, these are indispensable.
Thank you, I did the day.
Greetings to Ana Silvia.
Chavez Alfonso Rivero
September 14, 2010 12:35 hrs.
--- Oh, Hector - That is so sad. I remember walking with him-through the streets of Mexico City - Supporting and Trying to keep him the rhythm of historical walking going. I Was a Real Presence and Clearly much loved! Peer
Banek
CEO
Multiple Sclerosis International Federation
www.msif.org
September 14, 2010 12:36 hrs.
--- That is sad news
Hector. I am sorry to hear That, He Was Such a good man. I will email with my condolences Ninfa.
Zoe Burr Head of International Development
Multiple Sclerosis International Federation
London, England
September 14, 2010 4:31 hrs. ---
WITH MY GREATEST RESPECT, YOU CONTROL
UD. SRA NINFA a big hug, AT THIS TIME.
ING. GUSTAVO PONCE DE LEON AND FRANKLIN Mouriño
Montevideo, Uruguay
September 14, 2010 12:35 hrs. ---
Da
Although her special and beautiful and not us, that's the part I ask God q. Q give me strength if my husband were to die at a q I still believe God will heal my beloved commonwealth Martin. Greetings
Wendy
Central
September 14, 2010 12:24 hrs.
----
- -
Ninfa, relatives and friends of Manuel:
Partners Multiple Sclerosis:
Me very sad to know today the death of Manuel.
Ninfa, you command a hug and ask God to give you the strength to deal with deeply felt loss.
I remember fondly in our MS days.
EDMUND BARRAZA
CD. JUAREZ, CHIH.
Tuesday, September 14, 2010 12:18:31 pm
----
Rest in peace Manuel, I'll always remember. Our deepest condolences to Ninfa from all members be able to AC San Luis Potosi
Fernando Martínez Contreras
Support Group for People with Multiple Sclerosis PODRE AC
San Luis Potosí, SLP
Monday, September 13, 2010 8:48:30 pm
---
It is a great loss the departure of Sr.Manuel Meneses, but we have the example of support and understanding to our cause: Multiple Sclerosis, and her generosity and special love to our friend and sister, Ninfa, our prayers for God our Lord give his family an early resignation. A hug, Ninfa, we love you and join your pain ...
Ninfa: Durango joins your pain, we'll send you a hug with our prayers that God give you strength at this very difficult.
Ana Luisa Calzada Channels
Guadiana Association Multiple Sclerosis
Durango, Dgo.
Monday, September 13, 2010 8:33:10 pm
----
Dear President PARTNERSHIPS :
WANT THEM TO PARTICIPATE IN A VERY UNFORTUNATE NEWS TODAY MANUEL DIED IN THE MORNING ... Wife of our colleague and friend NINFA Monarrez, SI YOU BELIEVE IT CONVENIENT TO REACH Health, I imagine it will be VERY REWARDING TO KNOW THAT WE ARE WITH HER GREETINGS TO ALL AND SEE YOU BY GOD IN MONTERREY.
NAVA JOSE ALFREDO MARTINEZ
EMMEX Board Chairman 2008-2010
Monday, September 13, 2010 5:25:52 pm
----
Good afternoon, I just want
announce with great sadness
beloved of all of us with MS
Family This morning our great died
RIP
They're going to watch the funeral of the IMSS.
In the city of Guadalajara.
Greetings to all. Talpa
C. A. Gonzalez
In the photo-taken in Leon, Guanajuato, in May 2009 - appears with his wife Ninfa.
his absence hurts but I know that his spiritual progress continues, its existence is not limited to this world, but continues, and knowing I will achieve significant progress in their personal progress.
pray that their families and those we miss, when we receive comfort from our Lord.
command a special greeting to his widow Monarres Ninfa, my friend and inspiration to help others.
If someone wishes to express his condolences, is a wall of messages available in the blog
federation MS
associations Mexico EMMEX AC
http://emmex-ac.blogspot.com
federation MS
associations Mexico EMMEX AC
http://emmex-ac.blogspot.com
Manuel was a very special man, happy and jovial, a lover of life and excellent host. He suffered from Parkinson's disease for several years but that never prevented him from enjoying the sun and food, exercise and share with people.
Manuel was a master of life, retired from the armed forces of the United States, their physical strength will always beat the disease and even the delicate surgeries that were performed.
Mariano called him "my friend" and both are seeking to enter the pool or to raid the breakfast buffet. And Manuel walking with his walker or, as in the last year on his motorized wheelchair, Mariano wondered whenever we saw.
never forget the day I met Manuel, in 2007. He came driving to Cuernavaca. Ninfa only lowered the car and he said he would wait outside, but decided to join us. We sat under an orange tree in the garden and an impromptu lunch "turkey" (tamale pie) while Mariano was splashing around in the wading pool. And from that moment I could see in his face and the smile of Manuel that he was a man who would be worth learning.
Today is no longer with us but I know that someday return to eat a "turkey."
Pictured from left to right: Manuel Meneses, Héctor García Caballero, Ninfa Monarres (all three of Mexico), Margarita Ruiz of the National Multiple Sclerosis Association of Cuba. (Chicago, USA)
In November 2009, Ninfa Monarres de Mexico, was awarded the James D. MSIF Wolfensohn delivered to people with MS who are examples to others.
On that occasion, as always, Manuel went with her husband and supported. Proudly enjoyed international recognition that his wife was in Chicago, USA.
Like every time we met, Manuel was happy and friendly.
PHOTO: with Talpa Manuel Gonzalez, president of the Foundation Fegolo, Irapuato, Guanajuato. COMMENTS:
Dear Hector,
I just heard the sad news through this newsletter that you send me and I have been shocked.
remember so close to Manuel, in Guadalajara and the last time in Chicago ... always with his beloved nymph, helping all he could despite his limitations.
My most sincere condolences to the family of Mexican MS. A hug
Pedro Carrascal
Executive Director of the English Federation to Fight Multiple Sclerosis
September 14, 2010 15:56 hrs.
Thanks --- Hector:
Stories like yours and we have narrated in memory of Manuel, feed the soul and strengthen the spirit.
already Bertolt Brecht said: There are men who fight one day and are good, but there are men who struggle all their lives, these are indispensable.
Thank you, I did the day.
Greetings to Ana Silvia.
Chavez Alfonso Rivero
September 14, 2010 12:35 hrs.
--- Oh, Hector - That is so sad. I remember walking with him-through the streets of Mexico City - Supporting and Trying to keep him the rhythm of historical walking going. I Was a Real Presence and Clearly much loved! Peer
Banek
CEO
Multiple Sclerosis International Federation
www.msif.org
September 14, 2010 12:36 hrs.
--- That is sad news
Hector. I am sorry to hear That, He Was Such a good man. I will email with my condolences Ninfa.
Zoe Burr Head of International Development
Multiple Sclerosis International Federation
London, England
September 14, 2010 4:31 hrs. ---
WITH MY GREATEST RESPECT, YOU CONTROL
UD. SRA NINFA a big hug, AT THIS TIME.
ING. GUSTAVO PONCE DE LEON AND FRANKLIN Mouriño
Montevideo, Uruguay
September 14, 2010 12:35 hrs. ---
Da
Although her special and beautiful and not us, that's the part I ask God q. Q give me strength if my husband were to die at a q I still believe God will heal my beloved commonwealth Martin. Greetings
Wendy
Central
September 14, 2010 12:24 hrs.
----
Estimados todos:
Envío un fraternal abrazo a todos por la perdida tan lamentable de quien fuera el apoyo incondicional de nuestra compañera y amiga Ninfa Monárrez. Esperando el abrazo amable y consolador de nuestro Dios padre para que prontamente tengamos consuelo a los que quedamos en la lucha de la vida.
This morning we learned so heartfelt loss and Maria del Carmen and Jose Juan Segura server we send our condolences to the family of Mrs. Ninfa through this medium.
María del Carmen and a server Ninfa met at the last meeting of Presidents in 2009 in Leon, Guanajuato. So when he learned I was asked to reply immediately and send him their most sincere condolences to Ninfa, your family and friends. Therefore we share the grief felt by the extended family and especially EMMEX Ninfa, Mrs. inspired many causes and dreams.
With our most sincere respects
May God bless us all
María del Carmen and Jose Juan
Friends and relatives with multiple sclerosis
Ciudad Obregon, Sonora
September 14, 2010, 12:35:58 pm
- -
Ninfa, relatives and friends of Manuel:
Partners Multiple Sclerosis:
Me very sad to know today the death of Manuel.
Ninfa, you command a hug and ask God to give you the strength to deal with deeply felt loss.
I remember fondly in our MS days.
EDMUND BARRAZA
CD. JUAREZ, CHIH.
Tuesday, September 14, 2010 12:18:31 pm
----
Rest in peace Manuel, I'll always remember. Our deepest condolences to Ninfa from all members be able to AC San Luis Potosi
Fernando Martínez Contreras
Support Group for People with Multiple Sclerosis PODRE AC
San Luis Potosí, SLP
Monday, September 13, 2010 8:48:30 pm
---
It is a great loss the departure of Sr.Manuel Meneses, but we have the example of support and understanding to our cause: Multiple Sclerosis, and her generosity and special love to our friend and sister, Ninfa, our prayers for God our Lord give his family an early resignation. A hug, Ninfa, we love you and join your pain ...
Ninfa: Durango joins your pain, we'll send you a hug with our prayers that God give you strength at this very difficult.
Ana Luisa Calzada Channels
Guadiana Association Multiple Sclerosis
Durango, Dgo.
Monday, September 13, 2010 8:33:10 pm
----
Dear President PARTNERSHIPS :
WANT THEM TO PARTICIPATE IN A VERY UNFORTUNATE NEWS TODAY MANUEL DIED IN THE MORNING ... Wife of our colleague and friend NINFA Monarrez, SI YOU BELIEVE IT CONVENIENT TO REACH Health, I imagine it will be VERY REWARDING TO KNOW THAT WE ARE WITH HER GREETINGS TO ALL AND SEE YOU BY GOD IN MONTERREY.
NAVA JOSE ALFREDO MARTINEZ
EMMEX Board Chairman 2008-2010
Monday, September 13, 2010 5:25:52 pm
----
Good afternoon, I just want
announce with great sadness
and pain of the departure of a very
beloved of all of us with MS
Family This morning our great died
friend Mr. Manuel + (Husband of Ninfa)
RIP
They're going to watch the funeral of the IMSS.
Avenida de la Paz, before reaching Chapultepec
In the city of Guadalajara.
Greetings to all. Talpa
C. A. Gonzalez
Irapuato Walking With Multiple Sclerosis
September 13, 2010 13:49 hrs.
Tuesday, May 25, 2010
Something Witty To. Write In A Wedding Card
"Living with MS" on the Day of MS 2010
The National Institute of Neurology and Neurosurgery (INNN) "Manuel Velasco Suárez" invited us to participate in the program of activities organized to mark the World Day of Multiple Sclerosis, Wednesday May 26, 2010 in Mexico City.
IMAGE: Poster Day event
And I do extend an invitation to the entire community of people with MS to enjoy this free entry event, which begins at 10 am and ends at 2 pm .
I will be present at the event along with a group of people ZOE Association of Cuernavaca, but especially to accompany my wife Ana Silvia Barajas, who will have direct participation in the program.
Ana talk about his experience as a caregiver, their concerns, which has had to learn what course he likes and dislikes the way that changed his life to be caretaker a person with multiple sclerosis (MS), that is me.
activity INNN is coordinated in the area support groups and neuropsychology, who runs several years Dr. Yaneth Rodriguez Agudelo. The program is intensive, comprehensive and varied, with the intention that both patients and family members or caregivers, but also health professionals, learn more about living with multiple sclerosis.
In the multipurpose room at 10 o'clock, Dr. Jose de Jesus Flores, a welcome message will and will open the activity.
Then in the area outside the lounge, 9 tables of information, in which people interested in the topic of MS may receive information, contact details and even brief advice, be open for just over an hour.
The tables are on the following topics:
We look forward to having the presence of more people.
IMAGE: Sketch of the areas of INNN
The address is Avenida Insurgentes sur 3877, Col. La Fama, Tlalpan, Mexico DF 14269 · Tels ( 55) 5606 38 22 - 01 800 8321 825 - http://www.innn.salud.gob.mx/
And if you want to carpool from Cuernavaca, please send an email to eliwitz@hotmail.com with your contact information to tell hours. Thank you very much.
The National Institute of Neurology and Neurosurgery (INNN) "Manuel Velasco Suárez" invited us to participate in the program of activities organized to mark the World Day of Multiple Sclerosis, Wednesday May 26, 2010 in Mexico City. IMAGE: Poster Day event
And I do extend an invitation to the entire community of people with MS to enjoy this free entry event, which begins at 10 am and ends at 2 pm .
I will be present at the event along with a group of people ZOE Association of Cuernavaca, but especially to accompany my wife Ana Silvia Barajas, who will have direct participation in the program.
Ana talk about his experience as a caregiver, their concerns, which has had to learn what course he likes and dislikes the way that changed his life to be caretaker a person with multiple sclerosis (MS), that is me. PHOTO: Ana Silvia and I, in Chicago (November 2009)
activity INNN is coordinated in the area support groups and neuropsychology, who runs several years Dr. Yaneth Rodriguez Agudelo. The program is intensive, comprehensive and varied, with the intention that both patients and family members or caregivers, but also health professionals, learn more about living with multiple sclerosis.
In the multipurpose room at 10 o'clock, Dr. Jose de Jesus Flores, a welcome message will and will open the activity.
Then in the area outside the lounge, 9 tables of information, in which people interested in the topic of MS may receive information, contact details and even brief advice, be open for just over an hour. PHOTO: My mother Ana Maria and I
The tables are on the following topics:
- NURSING
RESPONSIBLE: Veronica Balcazar - REHABILITATION
RESPONSIBLE: Dr. Jorge Hernandez
ACTIVITY: Demonstration session - SUPPORT GROUPS AND NEUROPSYCHOLOGY
OBJECTIVE: To promote awareness of the public about multiple sclerosis and their emotional and cognitive consequences
RESPONSIBLE : Yaneth Rodriguez -
SOCIAL WORK ACTIVITIES: Wall newspaper and projected photographs -
RESPONSIBLE NEUROLOGY: Dr. Elizabeth Martinez - VIOLENCE
- PSYCHIATRY
RESPONSIBLE: Marian Spinola - ZOE MS association
OBJECTIVE: Diffusion and exposure - PHARMACEUTICAL ACTIVITY
: Broadcast Video
PROGRAM
11:25 photo projection that home visits made INNN
The INNN, led by Dr. Theresa Corona, who has a long history as a specialist treating MS, is a landmark health agency in our country: it emerge each year leading researchers and clinicians, but it is also an institution that provides high quality medical services in outpatient rehabilitation and hospitalization for people who do not have social security services and whose economy denies them access to private hospitals.
PHOTO: Main Entry INNN
11:45 Exhibition on Rehabilitation in MS
Rehabilitation is an indispensable part to be covered in the treatment of people with MS, because of the physical condition greatly depends on quality of life.
12:45 video projection of the pharmaceutical industry, and Yoga
specific medications used to treat MS were introduced in 1990 to the accelerated evolution. Steadily increasing supply of medicines and strengthening the research to find the best options, but the costs remain very high and inaccessible to most Mexican families.
The average monthly cost of specialty drugs for MS hovers around 2 000 500 USD.
is very important for the health sector of the Mexican government value the benefits that invest in these products are included in the basic drug long term because it is a very large profit, to avoid that young people have limited capacity for disease and retire early.
Regardless of the company that produces or distributes drugs for MS, they help people with MS have better quality of life, let's assets and represent a lower cost to the family economy, and in general to the economy our respective countries.
13:15 video projection "Living MS "
The video was provided by the English Federation to Fight Multiple Sclerosis, phellem, headed by our dear friend Pedro Carrascal.
was presented December 16, 2005, in the classroom Acts of the Ministry of Health in Madrid, the documentary produced by phellem "Living with Multiple Sclerosis."
13:45 Caregiver Experience
My wife, Ana Silvia became my caregiver when we started living together in 2005. I am a quadriplegic and I need help and care for all my activities and to meet needs physiological.
PHOTO: Mariano, Ana Silvia and I (November 2009)
Ana is also the mother of Mariano, who is now 7 years old. She, who studied journalism and communication sciences, had worked for 20 years in media and press offices and image, and even coordinated a children's culture. When I met her mother combined his duties with a few hours of class in the Universidad del Valle de Cuernavaca and advertising work in the agency creative synergy.
Today, Anne is devoted entirely to my care and Mariano, the home care, to chair the association ZOE and make social media work at the federation of EMMEX (Multiple Sclerosis Mexico, AC)
She has titled the talk that will occur in the INNN "I, Caregiver" , and frankly I do not know what I expect to hear, but knowing the passion that my wife has lived his life, no doubt it will be rewarding to witness their testimony of life with me, his testimony of life with multiple sclerosis.
14:10 gold clasp closure. Film Screening of World of MS, "Beautiful Day", with music by U2
------We look forward to having the presence of more people.
IMAGE: Sketch of the areas of INNN
The address is Avenida Insurgentes sur 3877, Col. La Fama, Tlalpan, Mexico DF 14269 · Tels ( 55) 5606 38 22 - 01 800 8321 825 - http://www.innn.salud.gob.mx/
And if you want to carpool from Cuernavaca, please send an email to eliwitz@hotmail.com with your contact information to tell hours. Thank you very much.
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