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NMO Diaries | Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder. By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest.

Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder. By sharing their stories, they hope to inspire others with

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NMO Diaries | Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder. By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. | nmodiaries.com Reviews
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NMO Diaries | Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder. By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. | nmodiaries.com Reviews

https://nmodiaries.com

Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder. By sharing their stories, they hope to inspire others with

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1

Getting back to the regular schedule program | NMO Diaries

http://www.nmodiaries.com/2015/08/11/getting-back-to-the-regular-schedule-program

Welcome to NMO Diaries. Christine, Erin, Jenna and Lelainia are ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. Become a Fan on Facebook! Update on Erin after 11 days in the hospital doing PLEX. August 25, 2016 Erin. August 8, 2016 Lelainia Lloyd. How to live with NMO and still enjoy your vacation. August 1, 2016 Christine. July 27, 2016 Jenna. July 18, 2016 Erin.

2

NMO Community | NMO Diaries

http://www.nmodiaries.com/nmo-community

Welcome to NMO Diaries. Christine, Erin, Jenna and Lelainia are ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. Become a Fan on Facebook! Update on Erin after 11 days in the hospital doing PLEX. August 25, 2016 Erin. August 8, 2016 Lelainia Lloyd. How to live with NMO and still enjoy your vacation. August 1, 2016 Christine. July 27, 2016 Jenna. July 18, 2016 Erin.

3

Family | NMO Diaries

http://www.nmodiaries.com/category/family-2

Welcome to NMO Diaries. Christine, Erin, Jenna and Lelainia are ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. Become a Fan on Facebook! Update on Erin after 11 days in the hospital doing PLEX. August 25, 2016 Erin. August 8, 2016 Lelainia Lloyd. How to live with NMO and still enjoy your vacation. August 1, 2016 Christine. July 27, 2016 Jenna. July 18, 2016 Erin.

4

Candace Coffee May you in RIP | NMO Diaries

http://www.nmodiaries.com/2015/07/11/candace-coffee-may-you-in-rip

Welcome to NMO Diaries. Christine, Erin, Jenna and Lelainia are ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. Become a Fan on Facebook! Update on Erin after 11 days in the hospital doing PLEX. August 25, 2016 Erin. August 8, 2016 Lelainia Lloyd. How to live with NMO and still enjoy your vacation. August 1, 2016 Christine. July 27, 2016 Jenna. July 18, 2016 Erin.

5

The first annual Dining for NMO Day is set for Oct. 19th | NMO Diaries

http://www.nmodiaries.com/2015/07/21/the-first-annual-dining-for-nmo-day-is-set-for-oct-19th

Welcome to NMO Diaries. Christine, Erin, Jenna and Lelainia are ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. Become a Fan on Facebook! Update on Erin after 11 days in the hospital doing PLEX. August 25, 2016 Erin. August 8, 2016 Lelainia Lloyd. How to live with NMO and still enjoy your vacation. August 1, 2016 Christine. July 27, 2016 Jenna. July 18, 2016 Erin.

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UNA NUEVA PRIMAVERA: JOHNS HOPKINGS NMO PATIENT DAY (DIA DEL PACIENTE CON NMO AUSPICIADO POR JOHNS HOPKINGS TRANSVERSEMYELITIS CENTER

http://unanuevaprimavera.blogspot.com/2014/09/johns-hopkings-nmo-patient-day-dia-del.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Viernes, 26 de septiembre de 2014. JOHNS HOPKINGS NMO PATIENT DAY (DIA DEL PACIENTE CON NMO AUSPICIADO POR JOHNS HOPKINGS TRANSVERSEMYELITIS CENTER. HOPKINGS TRANSVERSE MYELITIS CENTER. Una introducción al conocimiento de la NMO (. Janet Dean, CRNP), la...

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UNA NUEVA PRIMAVERA: EFECTO POSITIVO DEL TRATAMIENTO DE REFLEXOLOGIA EN LA CIRCULACION VENOSA DE UN PACIENTE CON NMO

http://unanuevaprimavera.blogspot.com/2014/03/efecto-positivo-del-tratamiento-de.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Jueves, 27 de marzo de 2014. EFECTO POSITIVO DEL TRATAMIENTO DE REFLEXOLOGIA EN LA CIRCULACION VENOSA DE UN PACIENTE CON NMO. Es conocido que los pacientes con. Venoso, así como la circulación linfática, sufren una disfunción (1). Y tres semanas de evol...

unanuevaprimavera.blogspot.com unanuevaprimavera.blogspot.com

UNA NUEVA PRIMAVERA: DIA INTERNACIONAL DE LAS ENFERMEDADES RARAS

http://unanuevaprimavera.blogspot.com/2015/02/dia-internacional-de-kas-ebfernedades.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Viernes, 27 de febrero de 2015. DIA INTERNACIONAL DE LAS ENFERMEDADES RARAS. El 28 de Febrero del 2015 se celebrará el. Día Internacional de las Enfermedades Raras. Han sido consideradas como. Enfermedad de Devic o Neuromielitis Optica. Desde este espac...

unanuevaprimavera.blogspot.com unanuevaprimavera.blogspot.com

UNA NUEVA PRIMAVERA: LA RIVOFLAVINA EN LA DIETA DE LOS PACIENTES CON NMO

http://unanuevaprimavera.blogspot.com/2015/04/la-rivoflavina-en-la-dieta-de-los.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Jueves, 9 de abril de 2015. LA RIVOFLAVINA EN LA DIETA DE LOS PACIENTES CON NMO. La rivoflabina (Vitañamina B2). Pertenece al grupo de las flavinas )pigmentos. Su descubrimiento se debió a un grupo de investigadores alemanes, quienes. 183; 1.R. Queso de...

unanuevaprimavera.blogspot.com unanuevaprimavera.blogspot.com

UNA NUEVA PRIMAVERA: PROBLEMAS ORTOPEDICOS DE LOS MIEMBOS INFERIORES EN LA NMO

http://unanuevaprimavera.blogspot.com/2014/11/problemas-ortopedicos-de-los-miembos.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Sábado, 22 de noviembre de 2014. PROBLEMAS ORTOPEDICOS DE LOS MIEMBOS INFERIORES EN LA NMO. Dicho paciente presentó dolor intenso en la planta del pie, enrrojecimiento y ardores en la misma, asícomo una casi imposibilidad en la marcha (que de hecho se e...

unanuevaprimavera.blogspot.com unanuevaprimavera.blogspot.com

UNA NUEVA PRIMAVERA: enero 2015

http://unanuevaprimavera.blogspot.com/2015_01_01_archive.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Domingo, 11 de enero de 2015. EL TRATAMIENTO DE REFLEXOLOGIA Y ALGUNOS TRANSTORNOS VISUALES EN LA NMO. Neuromielitis Optica (NMO) o enfermedad de Devic. En esta ocasión, presentamos algunos de los resultados obtenidos por Tokar y Nisembaum (2014) (1) al...

unanuevaprimavera.blogspot.com unanuevaprimavera.blogspot.com

UNA NUEVA PRIMAVERA: LOS NIVELES DE GLUTAMATO EN LAS LESIONES CEREBRALES...

http://unanuevaprimavera.blogspot.com/2011/04/los-niveles-de-glutamato-en-las.html

LAS HOJAS MARCHITAN CAEN, Y EL VIENTO LAS ARRASTRA FORMANDO REMOLINOS. CAEN LAS AMARILLAS HOJAS, NO HAY VERDOR, NI FRESCURA. ¿HABRA MUERTO EL ARBOL? NO, SOLO ES EL OTOÑO. ANA ALAS (Dedicado a los pacientes con Neuromielitis POptica o Enfermedad de Devic). Viernes, 29 de abril de 2011. LOS NIVELES DE GLUTAMATO EN LAS LESIONES CEREBRALES. O en su forma ionizada, el glutamato. Ionotrópicos: canales iónicos y receptores metabolotrópicos). En el cerebro en una serie de estados patológicos como los. Ya que est...

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List of #RareDisease Hashtags | RareConnect Support & Capacity Building

http://blog.rareconnect.org/social-media-case-studies/raredisease-list-of-hashtags

Social media case studies. Updates to RareConnect.org. List of #RareDisease Hashtags. March 24, 2016. Social media case studies. Hashtags make it easy to follow a conversation and unite a community around a particular rare disease, or just the #RareDisease. Topic in general. Here is a list of just some of the many rare disease hashtags that exist. Don’t see yours in the list? CMD (congenital muscular dystrophy). CRPS (Complex Regional Pain Syndrome). IPF (Idiopathic Pulmonary Fibrosis). Some people use t...

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NMO Diaries | Christine, Erin, and Jenna are young, ambitious women living with a rare neurological disorder. By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest.

Welcome to NMO Diaries. Christine, Erin, Jenna and Lelainia are ambitious women living with a rare neurological disorder, NMO (Neuromyelitis Optica). By sharing their stories, they hope to inspire others with medical challenges to live life to the fullest. Become a Fan on Facebook! June 26, 2017 Lelainia Lloyd. Putting the FUN in Fundraising! June 12, 2017 Lelainia Lloyd. This is for my #1 fan and caregiver. May 29, 2017 Christine. May 22, 2017 Jenna. Standing Up For Science. May 16, 2017 Lelainia Lloyd.

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