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Dos Voces, Un Destino: Don Vic

En El Salvador el Día de Los Padres se celebra el 17 de Junio.  Le contamos la historia de nuestro padre en su honor.

Don Vic

Don Vic

Victorino Rodezno nació en 1920, hijo de Pedro Rodezno y Isabel Callejas de Rodezno.   Ellos vivían en Tamanique, un pueblito como 20 kilometres de la costa en las montañas de El Salvador.  La familia Rodezno tiene raíces ondas en el pueblito.  La familia tenía potreros, fincas, una tiendita, y la cantina del pueblo.

Papá era el hijo mayor.   Él se crio durante el tiempo de la gran depresión.  Tiempo de muchas dificultades económicas.  Aunque la Familia Rodezno no eran pobres, la familia siempre acido trabajadora.  Trabajando los terrenos y la tienda.  Papá cuenta historias de mi abuelito, “El Viejito,” Papá Pedro.  Papá Pedro era conocido por ser con mucha compasión.  “Al viejito lo buscaban que fuera a curar la gente. Lo buscaban como médico.”  Papá discutía con su padre porque Papá Pedro era mujerío y alcolico.  Tomaba mucho; murió por el alcohol.    Papá le tenía mucho respeto y cariño a su mamá, “Chavelita.”  Mamá Chávela manejaba todo el negocio de la familia, cuidando ganado y atendiendo la tienda.

Cuando papá era jovencito, estaba ayudando a sacar el bálsamo.  El mecanismo se desprendió y le dio en la cabeza, quebrando la.  Todos pensaron que papá iba a morir pero el sobrevivió.  Papá todavía tiene la cabeza sumida donde se quebró el cráneo. Continue reading “Dos Voces, Un Destino: Don Vic” »

Family Dynamics – Facing a New Normal, Together

Family Dynamics When a loved one is diagnosed with Alzheimer’s disease there will almost certainly be issues relating to family relationships. First, normal roles change. A son suddenly becomes his mother’s caregiver, reversing their lifelong roles. Over time, a couple’s relationship changes as caregiving becomes the priority. Life plans, retirement plans, all the things you put off for the future, those things change and may in fact disappear completely. Roles of the caregiver change within their own family as well; a caregiver’s children may feel infringed upon when Grampa needs mom’s constant attention and focus. Continue reading “Family Dynamics – Facing a New Normal, Together” »

Summer Travel – Structure vs. Spontaneity!

3d illustration: Land and a group of suitcases. To take a vacation rentalWe hear from a lot of people about the challenges of traveling. While traveling can be a wonderful respite for everyone involved, especially in early stages of the disease, it does require special planning. Travel impacts routine, schedule and familiarity (with people and surroundings), all of the hallmark comfort criteria for people with Alzheimer’s. Changes in routine and location can trigger stress and disorientation. Each person’s situation is a bit different; talk with your loved one’s doctor about your particular travel plans.

General Travel Tips

Whether a quick trip in the car, or a long-distance trip across the country, a bag of essentials should always be at your side, including extra clothing, snacks, water, medications, activities and relevant toileting supplies. Carry meds in their original prescription bottles. Always carry emergency contact info, photocopies of important documents (insurance, medications, Power of Attorney, advanced directive) and a recent photo of your loved one (in case they wander). Have your loved one wear identification indicating that they have Alzheimer’s, or consider GPS enabled shoes if they won’t leave an ID on. Enroll in the MedicAlert® and Alzheimer’s Association Safe Return® program.

Consider an anti-anxiety medication for travel, and ask whether it is okay to take a “dry run” prior to the trip; some people experience side-effects. Perhaps even take a mini-trip trial run prior to a lengthier trip. Know your limitations and strength. If there have been difficult moments controlling agitation or anxiety in the past, realize that could re-occur. You should consider wearing identification yourself indicating you are a caregiver for an Alzheimer’s patient. If something happens to you, authorities know there is a possible issue with your loved one, especially when traveling.

Family Visits

Visiting family can take your loved one back to a place where they grew up, triggering forgotten memories as well as providing distant family a chance to re-connect. It can also provide respite to you as caregiver. Schedule lots of downtime, consider eating meals at home, and remain on a normal schedule. Can you bring your loved one’s pet, or a favorite pillow or blanket? Ask your host family members to “Alzheimer’s proof” their home. If relevant, prepare family members – especially children – for any hostile or unusual behaviors that may occur. If the host home is too chaotic, consider staying in a hotel so there will be a quiet retreat available.

Pleasure Visits/Touring

Minimize chaotic locations or activities where locations are constantly changing (sight-seeing tour). Disorientation can quickly occur, triggering stress and possible behavioral issues or wandering. There are logistics and safety concerns relating to transportation, hotels and meals.

If you decide your loved one and you are up to the task, you might still consider bringing help or looking into whether help is available at your destination point. As much as you can, have a Plan B, starting with travel insurance for the trip, in case a trip must be cancelled at the last minute. Some travel insurance may not cover dementia. Make all tickets refundable and changeable.

Many people travel with their loved one with the goal of respite for all. Unfortunately, sometimes that isn’t realistic. If respite is truly your goal, don’t feel guilty about scheduling your own trip as a break from your caregiving duties. Have a family member come to stay with your loved one while you take a break. Your mental refresh will help everyone involved.

Flying

Book your flights so you don’t have any tight connections or layovers. Allow extra time for everything. You might request a wheelchair whether your loved one needs it or not. TSA Cares is a free helpline to help you with any special needs relating to security screening and carryon luggage (should you need to bring medications or supplies). Book a middle seat for your loved one and keep the aisle seat for yourself; this enables you to keep them in their seat, while still allowing a trip to the restroom without climbing over other passengers. You should carry all documentation, including passports. Board early. If your loved one is in a late stage of Alzheimer’s you could consider a medical flight service.

Hotels

Notify your hotel that your loved one has Alzheimer’s. You may want to order room service until your loved one feels more acclimated. Bring a water-proof bed-pad for the hotel bed if incontinence is a concern. Bring a night-light to ensure a well-lit path to the bathroom. Purchase bells and tie on your loved one’s shoe strings or on the hotel door-knob, to alert you to potential wandering.

Bottom line is that a trip with your loved one can be a great idea if they are up to the trip and if you have a flexible and adaptable attitude. Don’t take things personally if it doesn’t work out, sometimes the break from routine is just too much for people to deal with. Once home, also recognize there will probably be an adjustment period before your loved one gets back into their pre-travel routine.

Staying Independent – “Help me help myself”

57278898_hi-rezAfter being diagnosed with Alzheimer’s disease, how long can you remain independent? In the early stages of the disease many people are able to retain their independence fairly well and the mental health benefits of remaining self-reliant are huge. Attempt to keep active and engaged, and continue doing the things you enjoy.

At the same time, it’s best to educate those around you about the changes that will occur as the disease progresses. Educating people helps them help you remain more independent. Talk to your employer about ways to continue working, perhaps reducing your hours or responsibilities. Ensure your home is safe; check your home for ways to reduce the chances of a fall or a fire. Consider finding alternatives to driving; remember the disease impacts your judgment as well as physical abilities, so you will have to make unpleasant adjustments as the disease progresses. Use the Alzheimer’s Navigator tool to help with mapping out your long-term care strategy, and get your legal and financial matters in order; do it while you can be an active participant and decision-maker. Continue reading “Staying Independent – “Help me help myself”” »

I’ve Just Been Diagnosed With Alzheimer’s. Can I Still Work?

buv006Due to an aging workforce, finding employees diagnosed with Alzheimer’s disease is becoming more common. While many people can remain at work in the early stages of the disease, each person’s situation is unique. Talk to your physician and caregiving team regarding how your current set of symptoms will impact your ability to work, and keep revisiting the conversation as your symptoms change. Depending on your particular job, you may need to transition out of work sooner than later, for example, if your job involves driving or utilizing skills that may be more challenging with Alzheimer’s.

If you are able to continue working, try to create a transition plan with your employer, perhaps reducing hours or taking a less demanding role. Educate your employer about the disease as you discuss your options, you may even want to bring a caregiver or advocate with you. You may find that your employer and even your Human Resources department may have had little training or exposure to the disease. Unfortunately, many companies that have stellar childcare benefits and support resources haven’t caught up with eldercare disease issues. Continue reading “I’ve Just Been Diagnosed With Alzheimer’s. Can I Still Work?” »

Dos Voces, Un Destino: La Señora Contenta

Para celebra el Día De las Madres le queremos contar un poco de la historia de nuestra mama.

Nuestra mamá nació en Chiltiupan, un pueblito en las montañas del Puerto De La Liberta. Nuestros abuelitos tenían una tienda y terrenos de agricultura. Mama Coro, nuestra abuela, se encargaba en el trabajo de la tienda y Papa Chuz en atender la finca y el ganado. Mamá es la hija menor de una familia de 13 hijos. Como la niña de la casa mamá se crio diferente a sus hermanas. Sus hermanas tenían que ayudar con el trabajo de la casa. Cuidando los hermanos menores, haciendo pan, queso, o bordando para vender. Nuestras tías nos cuentan de los pañuelitos que bordaban con corazones para vender en los bailes del pueblo. El oficio de mamá erra el trabajo de la tienda, atendiendo los clientes. A mamá le gustaba que la tienda estuviera alegre con música y cuando no habían clientes se ponía a pintar sus uñas.

La cultura Latina es dominada por el hombre, más en los tiempos cuando mamá se crió. Sus hermanos, todos fueron educados terminando sus estudios en la Universidad. Al contrario las hembra solo fueron a la escuela primaria o secundaria. Cuando Papa Chuz murió, a sus hijas no les dejo herencia. Sus pensamientos erran que a sus hijas, su esposo las tenían que mantener pero a sus hijos ellos tenía que mantener su familia. Gracias a Dios por su misma voluntad y por ser trabajadoras las hijas todas han salido adelante.

Irma y Victorino, 1963

Irma y Victorino, 1963

Cuando mamá se vino para Los Estados Unidos a reunirse con Papá era el año 1959. Sus hermanos le suplicaron que lo pensara bien lo que estaba haciendo, en Los Estados Unidos iba a tener que trabajar. El primer trabajo que encontró Mamá era en Los Angeles en una fábrica de sándwiches. Para trabajar allí mamá se tuvo que cortar sus uñas y lloro. Mamá tenía una cárstica fuerte, siempre diciendo “Que no hay que darle el brazo a torcer.” Entre poco tiempo mamá y papá se movieron a San Francisco donde encontraron trabajo en una laundry. Mamá es económica y en 1963 había ahorrado dinero para dar de entre en una casa. Ellos compraron una casita en Sur San Francisco donde nos creamos. Continue reading “Dos Voces, Un Destino: La Señora Contenta” »

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