Ready for Takeoff!

Posted on July 28, 2023 by Courtney Blewett

It’s that time of the year… travel season! Traveling is an exciting way to broaden your horizons, whether it be a day trip, visiting friends, or exploring a new city. The thought of traveling while having MS may be intimidating, but with plenty of planning and preparation, a fun-filled vacation is at your fingers tips, in spite of MS.

An MS diagnosis does not have to stop you from seeing the destination you’ve always wanted to visit. There are many ways to make traveling with MS less stressful and more accessible. Before traveling, have a conversation with your doctor and talk about any health concerns and how to plan and renew any medications you need to take with you.

If you’re traveling by plane, notify the airline ahead of time if you require a wheelchair or any specific accommodation. The airline can arrange transportation throughout the airport to your gate and can assist with expedited access through security.

When it comes to hotel accommodations, research the hotel ahead of time to ensure they have handicap-accessible rooms and an elevator. Consider booking a room on the ground level if you have limited mobility. Depending on how your medication is stored, confirm with the hotel if the room has a refrigerator so you can store any medications that require refrigeration.

Take time to research and plan your daily activities beforehand. You want to hit all the top sites that interest you and make the most of your trip! Write down the places you would like to visit and ensure these locations are handicap accessible or have elevator access. It’s important to incorporate rest breaks into your agenda so you do not overexert yourself and become fatigued. Don’t forget to hydrate too! Especially in warmer climates, overheating, and dehydration can be risk factors. Pack water bottles, and cooling devices, such as a cooling vest, to prevent overheating.

So, take that vacation you’ve been dreaming of and make it a reality! Don’t let Multiple Sclerosis stop you from traveling. With planning and preparation, anything is possible. At the same time, know your limits and plan accordingly. Enjoy and HAVE FUN!

Travel With MS

Posted on July 26, 2023 by MSAA

By Suzanne Marriott

` Two roads diverged in a wood and I –

I took the one less traveled by,

And that has made all the difference.

Robert Frost, The Road Not Taken

My husband, Michael, had MS, but that didn’t stop us from doing the things we loved, and the most important was travel. The challenge was learning how, not if, we could do it. Of course, we had to make many changes and accommodations in order to maintain this lifestyle.

When Michael was still walking, using his two hiking poles for balance, we bought a small, used RV and traveled up the coast of California, our home state. It was summer and I was free from my job as a teacher. As my husband’s caregiver, I made sure our little home on wheels was well stocked with all the things we would need, including all the paraphernalia that MS required.

But the day we were to leave, it was too hot and Michael realized he couldn’t drive in that heat. So our first accommodation was to embark on our trip in the evening, when it was cooler. As a former truck driver, Michael was used to driving at night, so off we went, enjoying the moonlight and a dearth of traffic.

With advance reservations secured, we stayed in California state parks in the parking areas authorized for persons with disabilities. This meant we were close to the toilet and shower facilities. All states have qualifications for their state parks’ disability status which provides many advantages, such as park-use discounts. For California information can be found at https://www.parks.ca.gov/30959.

There came a time when Michael could no longer walk. His HMO provided him with a power wheelchair, and we bought a used van with hand controls and a wheelchair ramp. Having the van meant that Michael was able to continue driving even as his disability increased. With some seat switching, I could also drive when needed. Soon we begin taking advantage of sightseeing closer to home. Living in the San Francisco Bay Area, this included the wine country, San Francisco itself, and the nearby coast and parklands. Sometimes we made longer trips, staying in motels and inns with accessible rooms. As always, the key was preparation and planning ahead.

For Michael and me, travel was something we refused to give up. The challenge was always figuring out how we could continue doing the things that we loved and what modifications we needed to make. Travel allowed us to continue having joy and fulfillment in our lives. If you’re thinking of travel, remember, it takes determination, creative thinking, and planning ahead. So go for it. And have fun!

Time To Go

Posted on July 26, 2023 by Teena Palathanam

It is that time of the year when people are enjoying the summer by traveling and exploring different destinations. Fatigue, bathroom issues, and walking difficulties are a few of the many challenges individuals with MS tend to encounter while traveling. Having MS should not deter you from traveling, it just means that your travel might need a little more detailed preparation and planning. It is important to note that individuals with disabilities have rights that are protected by the Americans with Disabilities Act (ADA) which prohibits discrimination and makes sure that accommodations are provided to such individuals whenever needed. Here are some tips to keep in mind that will make your travel experience relaxing and hassle-free:

Carry necessary medical paperwork: It is important to have a doctor’s note that details your MS diagnosis. Get all your prescriptions filled in by the neurologist. Carry medicines in daily pillboxes. Also, keep the contact information for your doctors saved on your phone in case you need to reach them in an event of an emergency.

Cooling products: Cooling vests, hats, pillows, and scarves are great to carry especially while traveling to places where the weather can fail to cooperate.

Rent mobility equipment: Mobility equipment like rollators, scooters, wheelchairs, walking aids, etc. can easily be rented. Renting equipment will avoid the hassle of carrying heavy gear. In many states, you can also have mobility equipment delivered right to your doorstep.

Air travel: While traveling by air, ask for wheelchair assistance while boarding and deplaning. Take advantage of early boarding procedures and seating accommodations. Use elevators and travelators (moving walkways) in the airports whenever possible.

Go with a travel buddy: Having a reliable travel partner can make your travel stress free. It will give you peace of mind just to know there is someone to give you a helping hand whenever you need one.

Seize every opportunity that comes your way and do not let MS stop you from experiencing the joy of travelling. There will always be some unexpected hiccups along the way but planning your travel ahead and knowing your rights will ensure that you have an unforgettable and memorable time.

Traveling with Health Issues

Posted on July 25, 2023 by MSAA

By Stacie Prada

My definition of travel has changed as my Multiple Sclerosis symptoms have progressed. Travel used to be trips that included overnight travel, and even one night away from home might not have qualified as “real” travel. Now travel includes going places for periods that disrupt my daily routines, and that means day trips solidly allow. Travel includes going anywhere outside of my normal routine. It demands having health issues considered and accommodated to ensure I have fun, meet my body’s needs, and don’t stress too much.

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Plan, Prepare, and Enjoy the Trip!

Posted on July 14, 2023 by Claudia Chavez

Are you planning a trip soon? Sure, getting to the destination is beautiful and all but what about all the planning that goes into the trip? Between the research, packing, reservations, and cost, traveling can be exhausting. Nothing beats an amazing vacation, but how do we make sure we are prepared for it all?

If you are anything like me, you will most definitely forget to pack something (and end up looking like a tornado tossing around the luggage to find it). Traveling with MS can be easy when you are prepared and have a contingency plan.

Here are some tips that can make your trip run as smoothly as possible.

Depending on your destination and needs, it may be a great idea to request a doctor’s note listing your medications and any specific medical needs you need accommodations for.
Bring the necessary storage devices, such as a cooler for injections, a needle clipping device, and storage must-haves.
Consider your medication dates if you take a DMT. For example, work around your infusion date.
Call the hotel in advance to verify the hotel has a refrigerator in the hotel room, or request a refrigerator for your room if you have medication that requires refrigeration.
Bring a list of your providers’ contact information just in case.
Bring extra medication in case you accidentally misplace it or damage it.
If you are traveling by air, you may contact the Transportation Security Administration (TSA) for additional information and to familiarize yourself with the Air Carrier Access Act (ACAA) that protects against discrimination.
Find MS support when traveling abroad by visiting the Multiple Sclerosis International Federation directory.

Knowing what to expect when traveling can ease your worries. Multiple Sclerosis doesn’t have to weigh you down. Don’t let anything stop you from taking that dream vacation you have always wanted. Plan, prepare, and enjoy the trip!

Travel Essentials

Posted on July 12, 2023 by Diana Cruz

Ahh summer-time. The (arguably) enjoyable weather brings about endless possibilities for outings, adventure, and quality time with friends and family. For many, the summer months indicate vacation and travel arrangements to sunny, tropical destinations. As appealing and worthwhile as a good getaway may be, these plans can also lead to uninterrupted thoughts about what to pack, what needs to get done, what to budget, feelings of guilt for leaving behind responsibilities, and an endless list of anticipated items. However, what many of us don’t think of packing is our well-being. Ensuring you are feeling your best self and are preparing in a way that will care for your mental health is just as essential as any other travel equipment.

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Take Control of Your Summer

Posted on June 30, 2023 by Courtney Blewett

Summertime is here and that means backyard barbecues, lounging on the beach or by the pool, outdoor fun, and leisurely walks. For many folks, these activities are enjoyable activities in the summer months. However, if you have Multiple Sclerosis, these activities on hot summer days can be challenging.

Exposure to warm temperatures can cause an exacerbation of symptoms for heat-sensitive individuals. It may feel like your world narrows during the summer season, but there are many ways to stay cool and reclaim the carefree feeling of the season.

Bring the beach to you! Sitting on the beach in the blazing sun may be the last place you want to be if you have heat sensitivity. So how about getting the “beach vibe” while still being cool at home? You can create the full scene right in the living room of your home. Grab a beach chair, turn on some feel-good music, and sit back and relax in the AC. Nowadays, there are a plethora of candles that have scents that smell just like the beach. They are so realistic, you’d swear you’re smelling the same thing!

Cook-in instead of a cookout! Bring your friends and the barbecue to the comfort (and coolness) of your home. Chop up some bright, fresh fruit and mix up some frozen yummy drinks. Order takeout instead of cooking by the stovetop, or perhaps one of your friends is a grill master and enjoys grilling up some goodies.

Enjoy the cool, late summer nights! One of the best parts of summer is the longer days and the cooler evenings. Take advantage of the breezy summer nights and sit outside. Watch nearby fireworks, or simply just sit and listen to the sounds of summer.

The summer months can be a challenging time for heat-sensitive individuals. The key is to plan ahead and do what makes you feel the most comfortable. Get creative and make your summer experience your own. Make this your best summer yet!

Summer Frozen S’mores

Posted on June 23, 2023 by Melissa Young

These frozen S’mores are the perfect treat for a hot summer day. They’re easy to make and ideal to keep in the freezer when you want a snack. Layers of chocolate pudding and marshmallow creme make these frozen S’mores the best summer treat for all!

Ingredients

1 box instant chocolate pudding 6 serving size
2.5 cups cold milk
16 graham crackers
7 oz marshmallow creme
4 oz cream cheese softened
8 oz frozen whipped topping thawed

Instructions

Line a 9×13 pan with parchment paper, allowing the piece to overhang on the edge of the pan.
Whisk together the pudding mix and milk in a medium bowl until smooth. Pour into a 9×13 pan and spread into an even layer.
Place in refrigerator to chill while you mix the marshmallow layer.
In a medium bowl, beat cream cheese and marshmallow cream until smooth. Fold in whipping topping gently.
Spread the marshmallow layer over the chilled chocolate layer and cover it.
Freeze layers for about 8 hours, until firm enough to cut through. Use the parchment paper to remove layers from the 9×13 pan and place them on a cutting board.
Break 16 graham crackers in half. This will allow for a top and bottom to make a sandwich. Slice pudding/marshmallow layers into 8 squares the same size as the graham crackers.
Sandwich the frozen square mixture between two graham crackers.

Be sure to store them in the freezer so they are ready to grab on the go and enjoy!!

Enjoy yourself, you deserve it.

Posted on June 21, 2023 by Claudia Chavez

It’s no secret that summer can be debilitating for those with MS. The heat and humidity can be a nightmare for so many of us. While everyone experiences summer differently, I think we can all agree that it’s important to plan head to ensure we are as comfortable as possible during these summer months.

Being prepared is more than bringing water, an umbrella, or a cooling vest. Being prepared also means understanding your limits and respecting them. It can be difficult to skip plans or cut them short when we need a break. It’s okay to sit down under the shade when our body is getting overheated. It’s okay to sit back and relax while friends and family continue with certain activities on their own. It’s okay to turn down plans when we know certain events will not sit well with our bodies. It’s okay to put your needs first.

Modifying certain activities can allow us to enjoy the outdoors this summer. Feel comfortable voicing your opinion when choosing a vacation destination, planning the activities for the day, or simply choosing the hotel bed closest to the air conditioner. Your voice matters.

Here are some things to keep in mind this summer:
• Do your research on the weather and humidity of the area.
• Notify your family and friends that you may need more breaks or downtime to relax.
• Declining to go to an event or activity you do not want to participate in or may be physically detrimental is self-care.
• Have fun and relax!

Summer is typically a time for fun and excitement and it’s easy to get wrapped up in the fun and forget that our bodies might need a bit more rest. Sharing your needs and feelings with your friends and family may help come up with a plan to ensure that everyone is safe and comfortable.

Beat The Heat

Posted on June 16, 2023 by Teena Palathanam

Summer is back with a bang and who does not want to have a little fun when the sun is all out and magnificent. Whether you are mowing the lawn, hiking a trail or bird watching, the heat can be harsh at times and it is good to figure out the best approach to tackle the heat. Especially for individuals with heat sensitive MS, the higher temperatures can trigger flare ups and exacerbations. Besides cranking up the AC, here are some cool and practical ways to beat the summer heat:

Cooling Accessories: Cooling accessories like vests, hats, scarves can be very useful for outdoor as well as indoor activities. Using neck, wrist and ankle coolers act quicker as the blood vessels in this area are in closer proximity to the skin thereby cooling the body at a much faster rate.

Cool drinks: The most important way to prevent dehydration is to hydrate. It is recommended to drink around eight cups of water every day. Always keep a bottle of water or any other preferred drink near you. If you want it to be cooler, add crushed ice to your drink or beverage.

Fans: Usage of ceiling fans, pedestal or tower fans can blow the hot air out and let the cool air in. Another easier and cost-effective alternative would be to open the windows on both sides of the house that will allow cross ventilation thereby bringing in the fresh breeze and cooling the house faster.

Swim: If you have access to a community pool near you, that’s the place to be. Besides, being a great physical activity, it can help to build muscle endurance and strength. You can even visit the local YMCA near you that will give you access to the pool.

Take a shower: A cold shower can be refreshing and can immediately lower the body temperature.

Wear the right colors: Stay away from darker colored clothing as they tend to retain more heat. Instead, opt for lighter summery shades like pink, blue, peach, pastels etc. Loose fitting cotton clothes can help you cool better.

Most importantly, do not forget to wear sunscreen while going outside. This summer whatever you plan on doing, I hope that you have one filled with sunshine and good times.

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