These good habits can help ease symptoms of peripheral neuropathy

A healthy diet, movement, and comfy footwear are among the tips

Ezekiel Lim avatar

by Ezekiel Lim |

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My mother-in-law, who has familial amyloid polyneuropathy (FAP), often experiences tingling and burning sensations as well as pain in her hands and feet. Because of that, she must keep them covered at all times. This is the reality of peripheral neuropathy.

She also experiences other symptoms that may be related to FAP or other ailments.

Neuropathy pain might seem to be beyond a patient’s control, but both a patient and their caregiver can adopt good habits to lower the frequency and severity of pain. This is one of the best services a caregiver can provide to improve their loved one’s quality of life.

Changing diet together

A neuropathy-friendly diet, which includes foods that improve a patient’s blood flow, can help. Foods high in omega-3 fatty acids, whole grains, fruits, vegetables, beans, and lean meats supply vitamins and amino acids, which are good for both blood flow and nerve repair.

One important aspect of a neuropathy-friendly diet is avoiding sugary foods and drinks, including diet soda. One of my mother-in-law’s worst habits is drinking too much diet soda. She has since started drinking more bottled water to counterbalance that, and as a result, has seen an improvement in both her symptoms and overall mobility.

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Avoiding alcohol is another good habit, and thankfully, my mother-in-law doesn’t drink it. In addition to the physical effects alcohol might have on nerves, its effect on cognitive function may lead patients to make poor decisions that put their bodies at risk of further discomfort.

As you may know, changing a diet can be tough emotionally, particularly when life is already hard because of FAP. (Comfort food, anyone?) So, if you’re a caregiver, consider joining your patient in dieting in an act of solidarity, even if it’s only when you eat with them.

Staying active

Remaining inactive is another bad habit that neuropathy patients might lean into, especially when pain makes them want to stay put. Caregivers might find it easy to overlook this because it relieves them of the responsibility of being active, too.

While it might be painful for neuropathy patients to move, staying sedentary might actually worsen neuropathy pain. Periodic movement like taking a few steps or simply moving the legs while seated can help.

If my mother-in-law’s legs or feet are not in pain, she’ll stand up and take a few steps every now and then.

Paying attention to footwear

Neglecting proper footwear is another bad habit that patients and their caregivers may unknowingly have. Comfortable footwear is crucial for patients suffering from peripheral neuropathy because it can decrease pressure on the lower extremities. Caregivers can help patients choose comfortable footwear that is easy to put on and take off. This may relieve the pressure of painful symptoms and help increase circulation.

My mother-in-law mainly wears New Balance walking shoes, which come in wider sizes and provide adequate cushioning and support. If she is experiencing more pain than usual, she’ll wear cushioned moccasins that are easy to slip into and don’t put too much pressure on the foot.

Practicing these habits can help patients stay comfortable, and it creates a framework for providing the best care. As with most things on a rare disease journey, good habits are best tackled with teamwork between caregivers and patients. You might need to change your habits little by little, but eventually, the changes will add up to benefits!


Note: FAP News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of FAP News Today or its parent company, Bionews, and are intended to spark discussion about issues pertaining to familial amyloid polyneuropathy.

Comments

Kraackss@gmail.com avatar

[email protected]

Thank you, this advice is helpful for myself and my caregiver.

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RuthBray avatar

RuthBray

I find wearing "Heat Holders" socks, or any other brand made for use in the snow, helps to keep my feet warm.

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James Huston avatar

James Huston

the best footwear that I have found is Mephisto. Their shoes were made for comfort on your feet. My Neurologist, who also has neuropathy, wears Mephisto shoes too. I was diagnosed with PN 10 years ago. I have a Vegan diet, no meat, nor dairy. I find that alcohol consumption exacerbates nerve pain and accelerates the decline in my cognitive function. I have cut all alcohol out of my regimen and feel so much better. I walk 1 mile a day. I use a rowing machine as my legs just can't use a stationary bike as I wear out too fast. I use the rowing machine for 40 minutes 5 times a week and lift weights 2 times a week. I agree with this article that Diet, Exercise, and a good pair of shoes make life much easier and my symptoms are much better.

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Joan Girdler avatar

Joan Girdler

Thank you for a great article! I don't quite know what is wrong so I read a lot hoping to garner information. I don't want and cannot afford a medical freight train.

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Jane Gay avatar

Jane Gay

Great tips. Does anyone know of a nerve stimulation machine at or above 150

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Ellen Marie avatar

Ellen Marie

I've had PN since 2011. It started mostly in my hands, but now my feet are hurting as well. I use gloves on my hands, the ones without finger tips. I've started experimenting with shoes. I recently purchased the neuropathy shies that are advertised on Facebook. I've only worn them for 2 days, but they are very comfortable and seem to help with the foot pain.

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Judy Burr avatar

Judy Burr

I agree with New Baance in wider size and exercise as much as body tolerates. Gabapentin helps me and I feel some patients like my sister give up to soon . Finally agreed to Pregabalin in low dose and is surprised it helps…(after pain got unbearable three years later.

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Lalia Perry avatar

Lalia Perry

My doctor told me not to exercise as trying to strengthen muscles would make things worse. This just seems wrong. Does anybody have a comment on this?

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