Unwanted Advice During the Holidays: How to Cope?

By: Meagan Freeman

During the holidays, we may find ourselves in the idyllic, peaceful scenes depicted in a Norman Rockwell painting. Surrounded by loving family and friends, sipping hot beverages and laughing by a crackling fire. Along with those scenes, we often partake in traditional meals, full of wonderful foods and desserts. The downside of this beautiful family tradition might be the hazards of incredibly high calorie, high fat, high sodium foods that may take a toll on those with multiple sclerosis.

For the past 6 months, I have made tremendous changes in my own diet. I have made fruits and vegetables the focus of my diet, along with low fat, low sodium options. I have worked very hard on maintaining this way of eating, and in general, have been supported by my family and friends in this process. In a few short months, I saw dramatic reductions in my blood pressure (I have hypertension in addition to MS,) and I have also seen large reductions in my cholesterol. In combination with my medication, I have reduced the severity of my MS symptoms through this lifestyle.

Why do the Holidays seem to completely derail healthy lifestyle choices? I have already begun to hear comments from family, such as: Why don’t you just take a break from the diet? Why don’t you skip a few days? What is the big deal? Why are you being so extreme? It is amazing how quickly “tradition” becomes the priority at holiday meals, rather than health. I am a believer in the concept that healthy meals can also be incredibly tasty.

In addition to these dietary comments, we may also find ourselves being showered with the ever-present “helpful advice” from family members about how to best manage our MS. “Have you tried———?” I happen to be a licensed family nurse practitioner, and even with my medical background, I have family and friends who ask me this very question constantly. They send me articles about new research, suggest different alternative and traditional therapies, and question my treatment decisions with regularity. Sometimes I feel a twinge of anger, and I have to hold back an emotional response. Instead, I find the response, “Thank you for letting me know about that, I will look into it,” to be the best.

Sticking to our choices while being gracious recipients of unwanted advice can be especially trying during the holidays. The most important thing to keep in mind is that we are loved and surrounded by people who only want the best for us. This is important to remember when you find yourself at the Thanksgiving dinner table receiving your 50th comment about the food (or lack of) on your plate!

Happy Holidays!

*Meagan Freeman was diagnosed with RRMS in 2009, at the age of 34, in the midst of her graduate education. She is a Family Nurse Practitioner in Northern California, and is raising her 6 children (ranging from 6–17 years of age) with her husband, Wayne. She has been involved in healthcare since the age of 19, working as an Emergency Medical Technician, an Emergency Room RN, and now a Nurse Practitioner. Writing has always been her passion, and she is now able to spend more time blogging and raising MS awareness. She guest blogs for Race to Erase MS, Modern Day MS, and now MSAA. Please visit her at: http://www.motherhoodandmultiplesclerosis.com.

Share Button
This entry was posted in Multiple Sclerosis Association of America and tagged , , , by MSAA. Bookmark the permalink.

About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

Leave a Comment

NAME:

EMAIL:

 SPAM PROTECTION: Sum of 1 + 10 ?

COMMENT: