It may surprise you that more boys and men are diagnosed with Eating Disorders than girls and women? Part of the reason for not reaching out is the stigma around Mental Health support and the lack of education about the disorder.
Eating Disorders are complex and treatment directed toward males can be limited. Helping someone overcome an Eating Disorder requires patience, therapy, or a stay at an in-house treatment center. I’ve only read a couple of books on Eating Disorders and will say it’s a very long road of relapses to reach recovery.
Due to their own stigma parents and family often overlook the early warning signs and do not reach out for help until it’s a crisis.
EATING DISORDERS IN MEN & BOYS
In the United States alone, eating disorders will affect 10 million males at some point in their lives. But due in large part to cultural bias, they are much less likely to seek treatment for their eating disorder. The good news is that once a man finds help, they show similar responses to treatment as women. Several factors lead to men and boys being under- and undiagnosed for an eating disorder. Men can face a double stigma, for having a disorder characterized as feminine or gay and for seeking psychological help. Additionally, assessment tests with language geared to women and girls have led to misconceptions about the nature of disordered eating in men according to the National Eating Disorder Association.
COMMON SYMPTOMS OF AN EATING DISORDER
Emotional and Behavioral Symptoms
In general, behaviors and attitudes that indicate that weight loss, dieting, and control of food are becoming primary concerns
Preoccupation with weight, food, calories, carbohydrates, fat grams, and dieting
Refusal to eat certain foods, progressing to restrictions against whole categories of food (e.g., no carbohydrates, etc.)
Appears uncomfortable eating around others
Food rituals (e.g. eats only a particular food or food group [e.g. condiments], excessive chewing, doesn’t allow foods to touch)
Skipping meals or taking small portions of food at regular meals
Any new practices with food or fad diets, including cutting out entire food groups (no sugar, no carbs, no dairy, vegetarianism/veganism)
Withdrawal from usual friends and activities
Frequent dieting
Extreme concern with body size and shape
Frequent checking in the mirror for perceived flaws in appearance
Extreme mood swings
Physical Symptoms
Noticeable fluctuations in weight, both up and down
Stomach cramps, other non-specific gastrointestinal complaints (constipation, acid reflux, etc.)
Menstrual irregularities — missing periods or only having a period while on hormonal contraceptives (this is not considered a “true” period)
Difficulties concentrating
Abnormal laboratory findings (anemia, low thyroid and hormone levels, low potassium, low white and red blood cell counts)
Dizziness, especially upon standing
Fainting/syncope
Feeling cold all the time
Sleep problems
Cuts and calluses across the top of finger joints (a result of inducing vomiting)
Dental problems, such as enamel erosion, cavities, and tooth sensitivity
Dry skin and hair, and brittle nails
Swelling around area of salivary glands
Fine hair on body (lanugo)
Cavities, or discoloration of teeth, from vomiting
Muscle weakness
Yellow skin (in context of eating large amounts of carrots)
Cold, mottled hands and feet or swelling of feet
Poor wound healing
Impaired immune functioning
The list of symptoms is long because it’s all-encompassing.
I encourage you to visit National Eating Disorder Association for a breakdown of the seven types of Eating Disorders and other behavioral and food concerns. Finding the underlying causes requires a trained professional in the right setting, an individual plan, and most importantly support from family and friends.
When looking for the right professional, talk with them about their approach and experience before introducing them to the patient. Finding the right approach may require research and time. It’s important to do this on the front end if possible. An approved method and training will make all the difference on the road to recovery. Disruptions during treatment can interfere with the recovery process making the patient resistant to continued treatment.
You’ve probably heard the term or worse yet suffer from Painsomnia yourself. If the term is new to you, here’s the short version. A person experiences insomnia due to pain preventing them from falling asleep or staying asleep.
“Sleep helps our bodies rest and heal, so good-quality sleep is vital for people with chronic illnesses. However, painsomnia can make a good night of sleep feel like a pipe dream. Fortunately, medical researchers are starting to learn more about the condition and how patients can cope.”
I have the type of Painsomnia that keeps me up after waking from pain and makes it impossible to go back to sleep. My sleep medicine has worn off by then and no it’s just pain against sleep, and sleep rarely wins.
I have tried several hacks to help go back to sleep with mixed results. I have an essential oil stick with a Lavander fragrance that’s supposed to relax you but I can’t tell it does any good. The one item that has worked this past week is Delta 8 gummies. I take one right after waking up and they do relieve stress and keep my mind from wondering allowing me to go back to sleep.
I have to point out that I’m living without pain medication right now so it can be a challenge when I have to sleep on my shoulders and hips. No back or stomach sleeping for me.
What can you do if you are struggling with Painsomnia?
Better Sleep Habits
The MD Anderson Sleep Center recommends that people adopt new habits into their nightly routine. These habits help form the foundation for good sleep hygiene:
Don’t use phones or computers before bed, as the blue light from the screen can disrupt sleep and cause eye strain.
Avoid taking long naps during the day.
Make your bedroom cool and dark.
Avoid eating heavy foods or exercising right before you sleep.
Sleep Aids
If you have trouble sleeping, your healthcare provider may prescribe sleep aids or encourage you to try over-the-counter medications. These drugs can help regulate your circadian rhythm and lull you into slumber. Melatonin supplements help regulate your sleep cycle.9
A study from Cureus journal found that ashwagandha, a medicinal herb, can help people fall and stay asleep.10
Prescription drugs may include benzodiazepines, which are often used to treat anxiety and insomnia. Before you try any new supplements or prescriptions, make sure to consult your healthcare provider.
Cognitive-behavioral therapy is a treatment that encourages people to rethink and change their behaviors. For people with insomnia, cognitive behavioral therapy may help,11
For example, a person without a sleep routine can work with a therapist to start better habits before bed. If anxious thoughts are keeping you up at night, cognitive behavioral techniques can teach you to stop those spiraling thoughts and focus on other, more restful thoughts.
If your painsomnia makes you feel helpless, those worries can make it even harder for you to get sleep. You may blame yourself or blame your body if you’re struggling with painsomnia. Cognitive behavioral therapy can help you cope with some of that frustration.
Hypnotherapy
While hypnotherapy is not a proven cure for painsomnia, some researchers have found that hypnosis might improve insomnia.12Hypnotherapy is an alternative medicine where practitioners use hypnosis and the power of suggestion to guide patients through various concerns.
Hypnotherapy is not a replacement for your healthcare provider or your current medications. Some researchers describe hypnotherapy as a sort of placebo. In either case, hypnosis can lull you into deep relaxation. This relaxation may help people with painsomnia fall asleep.
There’s no one size fits everyone but there are options for those who suffer from Painsomnia. I haven’t found the answer yet but did sleep until 2:00 AM this morning.
Some heartfelt advice from writer Bill Bernat, who’s been there
When I lived with severe depression and social anxiety, I found it extremely difficult to talk to strangers. Yet the one conversation that uplifted me more than any other occurred in the dining hall of the mental health wing of a mountain-town hospital. I met a woman who told me that a few days earlier, she’d driven her Jeep Wrangler to the edge of the Grand Canyon. She sat there, revving the engine and thinking about driving over.
She described what had been going on in her life in the days and months leading up, what her thoughts were at that exact moment, why she wanted to die, and why she didn’t do it. We nodded and half-smiled, and then it was my turn to talk about my journey to our table in that fine dining establishment. I had taken too many sleeping pills. After the doctors treated me, they were like, “Hey, we’d love it if you would be our guest in the psych ward!”
That day, she and I talked shop. She allowed me to be deeply depressed and simultaneously have a genuine connection to another person. For the first time, I identified as someone living with depression and I felt, oddly, good about it — or rather, like I wasn’t a bad person for having it.
Now, imagine one of the people at that table was a member of your family or a close friend who told you they were really depressed. Would you be comfortable talking to them?
Depression doesn’t diminish a person’s desire to connect with other people, just their ability.
The World Health Organization says that depression is the leading cause of ill health and disability worldwide, affecting more than 300 million people. In the United States, the National Institute of Mental Health reports 7 percent of Americans experience depression in a year. But while depression is super common, in my experience most folks don’t want to talk to depressed people unless we pretend to be happy. So we learn to put on a cheerful façade for casual interactions, like buying a pumpkin spice latte. The average barista doesn’t want to know that a customer is trapped in the infinite darkness of their soul.
Depression doesn’t diminish a person’s desire to connect with other people, just their ability. And despite what you might think, talking to friends and family living with depression can be easy and maybe fun. Not like Facebook-selfie-with-Lady-Gaga-at-an-underground-party fun — instead, I’m talking about the kind of fun where people enjoy each other’s company effortlessly, no one feels awkward, and no one accuses the sad person of ruining the holidays.
There’s a chasm that exists. On one side are people with depression, and on the other side is everyone else and they’re asking, “Why you gotta be so depressed?”
I’ve noticed there’s a chasm that exists. On the one side are those people living with depression, who may act in off-putting or confusing ways because they’re fighting a war in their head that nobody else can see. On the other side is everyone else, and they’re looking across the divide, shaking their heads, and asking, ‘Why you gotta be so depressed?’
I began battling depression when I was eight, and decades later, to my surprise, I started winning that battle. I shifted from being miserable much of the time to enjoying life. Today I live pretty well with bipolar disorder, and I’ve overcome some other mental health conditions, like overeating, addiction and social anxiety. As someone who lives on both sides of this chasm, I want to offer you some guidance based on my experiences to help you build a bridge across. I’ve also talked to a lot of people who’ve lived with depression to refine these suggestions.
Please don’t let our lack of bubbly happiness freak you out. Sadness doesn’t need to be treated with the urgency of a shark attack.
Before I get to the do’s, here are some some things you might want to avoid when talking to someone who’s depressed.
Don’t say “Just get over it.” That’s a great idea – we love it — but there’s just one problem: we already thought of that. The inability to “just get over it” is depression. Depression is an illness, so it’s no different from telling someone with a broken ankle or cancer to “just get over it.” Try not to fix us — your pressure to be “normal” can make us depressed people feel like we’re disappointing you.
Don’t insist that the things which make other people feel better will work for us. For example, you cannot cure clinical depression by eating ice cream, which is unfortunate because that would be living the dream.
Don’t take it personally if we respond negatively to your advice. I have a friend who, about a year ago, messaged me saying he was feeling really isolated and depressed. I suggested some things for him to do, and he was like, “No, no, and no.” I got mad, like, “How dare he not embrace my brilliant wisdom!” Then I remembered the times I’ve been depressed and how I thought I was doomed in all possible futures and everybody hated me. It didn’t matter how many people told me otherwise; I didn’t believe them. So I let my friend know I cared, and I didn’t take his response personally.
Don’t think that being sad and being OK are incompatible. Please don’t let our lack of bubbly happiness freak you out. Sadness does not need to be treated with the urgency of a shark attack. Yes, we can be sad and OK at the exact same time. TV, movies, popular songs and even people tell us if we’re not happy, there’s something wrong. We’re taught that sadness is unnatural, and we must resist it. In truth, it’s natural and it’s healthy to accept sadness and know it won’t last forever.
Talk to a depressed person as if their life is just as valuable, intense and beautiful as yours.
And here are some do’s.
Do talk to us in your natural voice. You don’t need to put on a sad voice because we’re depressed; do you sneeze when you’re talking to somebody with a cold? It’s not rude for you to be upbeat around us.
Do absolve yourself of responsibility for the depressed person. You might be afraid that if you talk to them, you’re responsible for their well-being, that you need to “fix” them and solve their problems. You’re not expected to be Dr. Phil — just be friendly, more like Ellen. You may worry that you won’t know what to say, but words are not the most important thing — your presence is.
Do be clear about what you can and cannot do for us. I’ve told people, “Hey, call or text me anytime, but I might not be able to get back to you that same day.” It’s totally cool for you to make a narrow offer with really clear boundaries. Give us a sense of control by getting our consent about what you’re planning to do. A while back when I was having a depressive episode, a friend reached out and said, “Hey, I want to check in with you. Can I call you every day? Or, maybe text you every day and call you later in the week? What works for you?” By asking for my permission, she earned my confidence and remains one of my best friends today.
Do interact with us about normal stuff or ask us for help. When people were worried about a friend of mine, they’d call him and ask if he wanted to go shopping or help them clean out their garage. This was a great way to reach out. They were engaging with him without calling attention to his depression. He knew they cared, but he didn’t feel embarrassed or like a burden. (Yes, your depressed friends could be a good source of free labor!) Invite them to contribute to your life in some way, even if it’s as small as asking you to go see a movie that you wanted to see in the theater.
This is, by no means, a definitive list. All of these suggestions are grounded in one guiding principle: speaking to someone like they belong and can contribute. That’s what allowed the woman in the Jeep Wrangler to start me on my path to recovery without even trying: She spoke to me like I was OK and had something to offer exactly as I was at that moment. Talk to a depressed person as if their life is just as valuable, intense and beautiful as yours. If you focus on that, it might just be the most uplifting conversation of their life.
Bill Bernat is a technology marketer, Comedy Central comedian, and The Moth Radio Hour storyteller living in Seattle. He brings awareness and humor to mental health in his award-winning show, Becoming More Less Crazy. He also leads storytelling workshops and fundraisers for nonprofit organizations.
From the Aromalief Blog, you might be surprised at the difference between the two.
Aromalief Team
In February of 2020, the popular prescription pain relief cream Voltaren changed to Over the Counter through a process at the FDA called Rx to OTC. This cream was first approved in 2007 to help temporarily relieve arthritis pain. In this blog post, I would like to share with you the ingredient differences between our cream Aromalief and Voltaren made by Novartis.
Aromalief Hemp Pain Relief Ingredients
Aromalief Hemp Pain Relief Cream combines the cooling power of naturally derived menthol with a blend of botanicals and nutrients. The preservatives used in Aromalief are non-toxic and help to prevent bacteria from growing in it.
Voltaren Gel’s active ingredient is Diclofenac Sodium which is a Non-Steroidal Anti-Inflammatory Drugs also known as NSAIDs. Also included in the formula is Ammonia.
ACTIVE INGREDIENTS
DICLOFENAC SODIUM
INACTIVE INGREDIENTS
AMMONIA, CARBOMER HOMOPOLYMER TYPE C, COCO-CAPRYLATE/CAPRATE, ISOPROPYL ALCOHOL, MINERAL OIL, POLYOXYL 20 CETOSTEARYL ETHER, PROPYLENE GLYCOL, WATER
Annabell wrote this post in response to the questions she received on their Facebook page.
I can speak from personal experience: Aromalief works like no other topical cream I’ve used. Soon after I rub the cream on, it begins to warm up and has a light menthol and lavender scent. Nothing overpowering. I joke all the time that my dogs would not know it’s me without the Aromalief scent.
Aroalief is for tired, achy muscles, arthritis, fibromyalgia, and neuropathic pain. I even use it for my carpal tunnel in both hands.
Three things I’ve learned since having the opportunity to review Aromalief for Chronic Illness Bloggers are that she strives for excellence, guarantees 100% customer satisfaction, and is committed to the pain community. The bonus for me is that Aromalief is WOMEN-owned and made in America.
Here’s a copy of my review for Aromalief Lavender Hemp Pain Cream.
If you have any questions for Annabell, please write to her at Aromalief.
Earlier in the month I was diagnosed with persistent Hypocalcemia. The lack of calcium can cause many problems but the most troubling to me at this time is more Osteoporosis which I already have in my hip and heart complications, which I already have several heart issues.
Like everyone my appointment was pushed out and we wait out the social distancing to get back to normal. I’m lucky that I don’t have the worst symptoms yet.
Calcium is a vital mineral. Your body uses it to build strong bones and teeth. Calcium is also needed for your heart and other muscles to function properly. When you don’t get enough calcium, you increase your risk of developing disorders like:
It’s important to ensure proper calcium intake at all ages.
For children and teenagers, the recommended daily allowances for calcium are the same for both sexes. According to the National Institutes of Health (NIH), the daily allowances are:
Women need to increase their calcium intake earlier in life than men, starting in middle age. Meeting the necessary calcium requirement is particularly important as a woman approaches menopause.
The hormone disorder hypoparathyroidism may also cause calcium deficiency disease. People with this condition don’t produce enough parathyroid hormone, which controls calcium levels in the blood.
During menopause, women should also increase their calcium intake to reduce the risk of osteoporosis and calcium deficiency disease. The decline in the hormone estrogen during menopause causes a woman’s bones to thin faster.
Other causes of hypocalcemia include malnutrition and malabsorption. Malnutrition is when you’re not getting enough nutrients, while malabsorption is when your body can’t absorb the vitamins and minerals you need from the food you eat. Additional causes include:
low levels of vitamin D, which makes it harder to absorb calcium
medications, such phenytoin, phenobarbital, rifampin, corticosteroids, and drugs used to treat elevated calcium levels
“Hungry bone syndrome,” which may occur after surgery for hyperparathyroidism
removal of parathyroid gland tissue as part of surgery to remove the thyroid gland
If you miss your daily dose of calcium, you won’t become calcium deficient overnight. But it’s still important to make an effort to get enough calcium every day, since the body uses it quickly. Vegans are more likely to become calcium deficient quickly because they don’t eat calcium-rich dairy products.
Calcium deficiency won’t produce short-term symptoms because the body maintains calcium levels by taking it directly from the bones. But long-term low levels of calcium can have serious effects.
Calcium deficiencies can affect all parts of the body, resulting in weak nails, slower hair growth, and fragile, thin skin.
Calcium also plays an important role in both neurotransmitter release and muscle contractions. So, calcium deficiencies can bring on seizures in otherwise healthy people.
If you start experiencing neurological symptoms like memory loss, numbness and tingling, hallucinations, or seizures, make an appointment to see your doctor as soon as possible.
Contact your doctor if you have symptoms of calcium deficiency disease. They’ll review your medical history and ask you about family history of calcium deficiency and osteoporosis.
If your doctor suspects calcium deficiency, they’ll take a blood sample to check your blood calcium level. Your doctor will measure your total calcium level, your albumin level, and your ionized or “free” calcium level. Albumin is a protein that binds to calcium and transports it through the blood. Sustained low calcium levels in your blood may confirm a diagnosis of calcium deficiency disease.
Normal calcium levels for adults can range from 8.8 to 10.4 milligrams per deciliter (mg/dL), according to the Merck Manual. You may be at risk for calcium deficiency disease if your calcium level is below 8.8 mg/dL. Children and teens typically have higher blood calcium levels than adults.
Calcium deficiency is usually easy to treat. It typically involves adding more calcium to your diet.
Do not self-treat by taking a lot of calcium supplements. Taking more than the recommended dose without your doctor’s approval can lead to serious issues like kidney stones.
Commonly recommended calcium supplements include:
calcium carbonate, which is the least expensive and has the most elemental calcium
calcium citrate, which is the most easily absorbed
calcium phosphate, which is also easily absorbed and doesn’t cause constipation
It’s important to note that some medications could interact negatively with calcium supplements. These medications include:
blood pressure beta-blockers like atenolol, which may decrease calcium absorption if taken within two hours of taking calcium supplements
antacids containing aluminum, which may increase blood levels of aluminum
cholesterol-lowering bile acid sequestrants such as colestipol, which may decrease calcium absorption and increase the loss of calcium in the urine
estrogen medications, which can contribute to an increase in calcium blood levels
digoxin, as high calcium levels can increase digoxin toxicity
diuretics, which can either increase calcium levels (hydrochlorothiazide) or decrease calcium levels in the blood (furosemide)
certain antibiotics such as fluoroquinolones and tetracyclines, whose absorption can be decreased by calcium supplements
Sometimes diet changes and supplements aren’t enough to treat a calcium deficiency. In this case, your doctor may want to regulate your calcium levels by giving you regular calcium injections.
You can expect to see results within the first few weeks of treatment. Severe cases of calcium deficiency disease will be monitored at one- to three-month intervals.
You can prevent calcium deficiency disease by including calcium in your diet every day.
Be aware that foods high in calcium, such as dairy products, can also be high in saturated fat and trans fat. Choose low-fat or fat-free options to reduce your risk of developing high cholesterol and heart disease.
While meeting your calcium requirement is very important, you also want to make sure you’re not getting too much. According to the Mayo Clinic, upper limits of calcium intake in milligrams (mg) for adults are:
2,000 mg per day for men and women 51 years of age and up
2,500 mg per day for men and women 19 to 50 years of age
You might want to supplement your diet by taking a multivitamin. Or your doctor may recommend supplements if you’re at high risk for developing a calcium deficiency.
Multivitamins may not contain all of the calcium you need, so be sure to eat a well-rounded diet. If you’re pregnant, take a prenatal vitamin.
Vitamin D
Vitamin D is important because it increases the rate calcium is absorbed into your blood. Ask your doctor how much vitamin D you need.
To increase your calcium intake, you can add food rich in vitamin D to your diet. These include:
I’ve recently been diagnosed with the immune disorder Hypogammaglobulinemia which requires the expertise of an Endocrinologist. My doctor isn’t sure how I contracted it since I don’t fit any noted categories.
Infusion treatments may become necessary for Hypogammaglobinemia, some patients only require one treatment and others require ongoing infusion treatment for life.
Hypogammaglobulinemia is a problem with the immune system that prevents it from making enough antibodies called immunoglobulins. Antibodies are proteins that help your body recognize and fight off foreign invaders like bacteria, viruses, and fungi.
Without enough antibodies, you’re more likely to get infections. People with Hypogammaglobulinemia can more easily catch pneumonia, meningitis, and other infections that a healthy immune system would normally protect against. These infections can damage organs and lead to potentially serious complications.
Several gene changes (mutations) have been linked to Hypogammaglobulinemia.
One such mutation affects the BTK gene. This gene is needed to help B cells grow and mature. B cells are a type of immune cell that makes antibodies. Immature B cells don’t make enough antibodies to protect the body from infection.
THI is more common in premature infants. Babies normally get antibodies from others through the placenta during pregnancy. These antibodies protect them from infections once they’re born. Babies that are born too early don’t get enough antibodies from their mothers.
A few other conditions can cause Hypogammaglobulinemia. Some are passed down through families and start at birth (congenital). These are called primary immune deficiencies.
They include:
ataxia-telangiectasia (A-T)
autosomal recessive agammaglobulinemia (ARA)
common variable immunodeficiency (CVID)
hyper-IgM syndromes
IgG subclass deficiency
isolated non-IgG immunoglobulin deficiencies
severe combined immunodeficiency (SCID)
specific antibody deficiency (SAD)
Wiskott-Aldrich syndrome
x-linked agammaglobulinemia
More oftenTrusted Source, Hypogammaglobulinemia develops as a result of another condition, called secondary or acquired immune deficiencies. These include:
If your Hypogammaglobulinemia is severe, you may get Immune Globulin replacement therapy to replace what your body isn’t making. You get this treatment through an IV. The immune globulin comes from the blood plasma of healthy donors.
lemon, ginger, and turmeric paper-thin using a mandolin or sharp knife. Layer slices in a half-pint jar. Break cinnamon sticks lengthwise into several pieces and tuck them in jar. Add apple cider vinegar.
Pour
Pour honey into the jar, covering the other ingredients. Place jar in the refrigerator. The honey becomes thin syrup and read to use in 12 hours.
To Use
Stir up 1/4 cup into a hot tea or water: or take 1-2 tsp. syrup each hour as needed to soothe sore throat or cough. Shake the jar occasionally. Keep Refrigerated for up to three weeks.
BONUS Grannies Recipe
Mix equal parts honey, whiskey and lemon. Refrigerate in a pint jar, leave a spoon in and take a spoonful or two every time your throat needs it.
Super Bonus Gramps Recipe
Keep the bottle of Black Velvet on the nightstand, when you wake yourself up coughing, take a sig.
Welcome to Remedy, a blog by U.S. Pain Foundation. Remedy aims to provide people with the support they need to thrive despite chronic pain. It features the information about promising treatments, tips and strategies for self-management, resources for coping with the emotional and social effects of pain, unique perspectives from patients, clinicians, and caregivers–and much more. To submit an article idea, email contact@uspainfoundation.org.
If your child feels tired and achy, you may not worry initially. After all, there’s nothing urgent about what seems to be mild, general discomfort. However, if your child is constantly in pain, exhausted, having trouble sleeping, and experiencing intense moods, he/she may have fibromyalgia.
This condition is fairly common in adults, but parents and clinicians may overlook the possibility of juvenile primary fibromyalgia syndrome — that is, fibromyalgia in children.
JUVENILE FIBROMYALGIA SYMPTOMS TO WATCH OUT FOR
Fibromyalgia is a chronic condition characterized by pain and fatigue. According to experts, children will often describe this pain as “stiffness, tightness, tenderness, burning or aching.” This pain can last for months and is often accompanied by other symptoms that affect a child’s overall well-being, energy level, and emotional health, including:
Tender spots on muscles
Difficulty sleeping and fatigue
Aches, including stomachaches and headaches
Lack of focus or memory
Anxiety and depression
If your child is experiencing these symptoms, you should see a doctor. There’s not one test to confirm it, so he/she will go through a range of tests to rule out other conditions.
Unfortunately, there is no one “cure” for fibromyalgia, which can be frustrating for patients, especially children. If left untreated, symptoms can lead to issues at school or making friends. Many parents describe this as a “vicious cycle” where symptoms continue to feed the condition.
Experts still aren’t sure what causes fibromyalgia or how it develops in the body. Some believe that mixed-up pain signals in the brain cause greater pain chemicals and/or overactive pain receptors. Others think it might be triggered, in part, by an emotional event like an illness, injury or psychological stress. But even if the cause involves emotions, the pain is still real.
HOW CHILDREN CAN COPE WITH FIBROMYALGIA
It’s important to create a support team and get your child’s primary care doctor, pain specialist, psychologist, physical therapist, and teachers on board. The more people are aware of your child’s condition, the more they can help him/her cope with symptoms at home and school. You may also want to look for pain support groups near you, for both your child and you as a parent.
Your doctor can help you decide whether medication, such as anti-inflammatories, antidepressants, or nerve pain medications, may be right for your child. He or she also may recommend therapies like injections or topical creams. In conjunction with these interventions, your doctor will probably prescribe treatments like physical therapy and behavioral changes, which are crucial to long-term management of fibromyalgia.
Let’s go over some nonpharmacological strategies for coping with fibromyalgia.
FIVE STRATEGIES FOR IMPROVED SYMPTOMS
Although fibromyalgia may disrupt your child’s life, affecting school and friendships, you may be able to improve your child’s quality of life with these natural therapies and changes. Of course, there’s no cure for fibromyalgia, but by managing symptoms, you can help your child get back to some sense of normalcy.
Get moving!
Exercise can be incredibly valuable for managing your child’s fibromyalgia symptoms. Exercise can relieve muscle stiffness and tire out the body physically so that your child can fall asleep more easily. In particular, pool exercises have been shown to help patients because the warm water can have a soothing effect on pain and also promote blood circulation.
Consider signing up your child for swim class to get regular exercise that is both fun and good for symptoms. Start with limited intervals of exercise at first, and slowly increase them as symptoms allow. Aquatic physical therapy can be extremely beneficial for patients whose fibromyalgia is too severe for regular pool activities.
Incorporate meditation methods
While your child may not be interested in meditation, try to incorporate some of the practices in your child’s daily life. After playtime, encourage your child to take a moment to relax and reset. In addition, teach your child how to use relaxing breathing exercises when he/she feels overwhelmed during school or before bed.
Studies show that meditation can help reduce fibromyalgia patients’ stiffness, anxiety and depression. In the least, promoting a stress-free environment and creating a sense of relaxation will help your child feel less anxious.
Say goodnight to fibromyalgia
Your child’s sleep routine is essential for improving fibromyalgia symptoms. Chart out the best routine for your child together. Make sure he/she goes to bed at the same time every day and start “sleep-ready” habits an hour before bed. This routine could include a break from screen time, reading a story together, listening to a relaxing song and/or taking a hot bath. Promoting a relaxing environment will help your child get to sleep.
Make sure you’re not giving your child food late at night, especially items with any caffeine or sugar. Also, be sure take away tablets and cell phones. The blue light can wake up your child instead of helping him/her get sleepy. Sufficient sleep is essential to managing pain.
Change your child’s diet for success
Some experts recommend following an anti-inflammatory diet to prevent aches and pains. In general, an anti-inflammatory diet is based on the Mediterranean diet, which emphasizes fish, fish, vegetables, whole grains, and olive oil.
Update your child’s lunch to include a handful of nuts, or add an apple for a snack. Anytime you can add fruits and vegetables to his/her diet, do it! This boost of nutrients will fuel your child for success. Try to limit junk food as well, which has no value and could actually inflame your child’s pains.
Schedule your child for a physical therapy session
Your child could benefit from seeing a physical therapist or chiropractor near you. Recent studies show how physical therapy or chiropractic can have a positive impact on fibromyalgia patients. Finding the right physical therapist is important. Call in advance to ensure they have experience with fibromyalgia and/or with children. Specific exercises in physical therapy can help to improve your child’s core strength and incorporate techniques to soothe muscle aches and pain. Similarly, regular massage therapy sessions with an experienced masseuse can improve your child’s exercise, sleep and mood.
TALK TO YOUR DOCTOR
A fibromyalgia diagnosis can be challenging, but doesn’t have to take over your child’s life. It’s a good idea to talk to an expert to come up with the most effective care plan for your child, one that ideally includes a diverse range of strategies, like those listed above. Together, you can talk about your child’s specific issues and needs, and figure out the best way to improve symptoms.
About Dr. Brent Wells
Dr. Brent Wells is a graduate of the University of Nevada where he earned his bachelor of science degree before moving on to complete his doctorate from Western States Chiropractic College. He founded Better Health Chiropractic and Physical Rehab in Anchorage in 1998. He became passionate about being in the chiropractic field after his own experiences with hurried, unprofessional healthcare providers. The goal for Dr. Wells is to treat his patients with care and compassion while providing them with a better quality of life through his professional treatment.
These incredible pups catch poachers, sniff out invasive plants and diseases, and more, thanks to the work of wildlife biologist and conservation-dog expert Megan Parker.
What happens to those dogs that are just too much dog for people to handle? “You know them — you go to your friend’s barbecue, their dog is so happy to see you that she pees on your feet, and she drops a slobbery ball in your lap,” says Megan Parker (TEDxJacksonHole talk: Dogs for Conservation), a wildlife biologist and dog expert based in Bozeman, Montana. “You throw it to get as much distance between you and the dog as possible, but she keeps coming back with the ball. By the 950th throw, you’re thinking, Why don’t they get rid of this dog?” All too often, their owners reach the same conclusion and leave their pet at a shelter.
Thanks to Parker and the team at Working Dogs for Conservation (WD4C), some of these dogs have found a new leash lease on life. They’re using their olfactory abilities and unstoppable drive in a wide variety of earth-friendly ways, working with human handlers to sniff out illegal poachers and smugglers, track endangered species, and spot destructive invasive plants and animals.
Chai is shown here with a trainer. After a dog learns to recognize a particular scent, the education isn’t over — their handler works with them regularly so they maintain their skills. These days, you can find this sweet German shepherd protecting wildlife in Zambia, along with her brother Earl.
Parker first considered using dogs in conservation when she worked on the reintroduction of wolves to Yellowstone Park and was asked how researchers could track wolves through their scat, or droppings. “I started thinking how best to detect their scat off a large landscape, and the idea came up for dogs,” she says. In 2o00, she cofounded WD4C to train and use canines in conservation work. Most of their dogs are adopted from shelters or from organizations or work settings where they didn’t quite fit in.
While it’s fair to say almost all dogs love toys, wildlife-detection dogs areobsessed with them. “They’ll do anything to chase a ball or a tug toy,” says Parker. If their preferred plaything is thrown far into the brush or buried in a massive pile of leaves, no worries — they won’t stop looking until they find it. No food, obstacle or distractions can deter them, and WD4C staff have turned this single-minded focus into a powerful incentive. Their canine friends are rewarded with their favorite toy every time they locate a desired wildlife-related scent, anything from elephant ivory and poachers’ guns in Zambia and trafficked snow leopards in Tajikistan to predatory Rosy wolf snails in Hawaii and invasive Argentine ants on California’s Santa Cruz Islands. The dogs are careful not to disturb or touch any specimens they pinpoint; it’s all about the toy.
Lily, a yellow Lab, is one of the group’s many sad-start-happy-ending stories. When the then-three-year-old came to the attention of WD4C trainers, she’d already bounced her way in and out of five different homes. She couldn’t sit still and she never, ever wanted to stop playing. Oh, and she was a bit of a whiner. Since joining WD4C in 2011, she has been trained to recognize a dozen different conservation-related scents and been deployed to track grizzly bears and sniff out the eggs, beetles and larvae of emerald ash borers, an insect that has killed millions of trees in the US and Canada.
Hilo was originally meant to be a guide dog for the blind, but when that didn’t work out, he found a place at WD4C. Here, he wears the standard orange vest that tells conservation dogs it’s time to get to work. Hilo helps detect quagga and zebra mussels on boats.
The three-dozen-strong WD4C pack also includes purebred working dogs who weren’t right for their intended occupations. Orbee, a border collie, had the enthusiasm and live-wire energy required of ranch dogs, but there was one problem: he had zero interest in herding sheep. He also barked a lot. Since joining WD4C in 2009, Orbee has had a globe-trotting career — he has spotted invasive quagga and zebra mussels on boats in Alberta and Montana, monitored the habitats of the endangered San Joaquin kit fox in California, and assisted scientists in northern Africa in counting up Cross River gorillas, the world’s rarest gorilla.
Jax is a Belgian malinois, a sturdy breed frequently used by the police and military. He was in training to serve with the US Army’s special unit, the Green Berets, until his handlers realized Jax doesn’t like to bite people — just toys. And, boy, does he loves toys; he’s even tried to climb trees to reach prized objects. Since 2017, Jax’s athleticism and high spirits have been used by the WD4C to perform tasks such as mapping the movements of bobcats in the western US.
Tule gets to roam the great outdoors for WD4C, using her keen nose — dogs have around 300 million olfactory receptors compared to humans’ 6 million — to track animals such as the endangered black-footed ferret in Wyoming.
“Different dogs have different strong suits,” says Parker. She and the WD4C team try to place their charges in environments that match their skillset, likes and dislikes. Unlike many dogs, Tule (above), a Belgian malinois who flunked out of a job with US Customs and Border Patrol, has absolutely no desire to chase small animals such as cats, squirrels and rabbits. This made her the perfect fit to help researchers monitor black-footed ferrets, which live in the same territory as a large, scampering prairie-dog population. The ferrets, once thought extinct in the US, were reintroduced in Wyoming in recent years. Tule alerts her handlers to the scent of live ferrets or their scat, information that allows state wildlife officials to map their distribution and see if the population is recovering. Without Tule and her pack, researchers would be forced to study the elusive creatures with cameras or live traps, undependable methods at best.
The dogs’ efforts have resulted in positive, substantial changes. The organization teamed up with the nonprofit Wildlife Conservation Society so their dogs could track the scat of four keystone carnivores (grizzly bears, black bears, mountain lions and wolves) through the Centennial Mountains in Idaho and Montana. Five years of doggie data showed that all four species depended on the mountains to move between the Greater Yellowstone ecosystem and central Idaho wilderness areas. Thanks to this information, activists were able to stop construction of a housing development that would have interrupted their migratory pathway.
Tobias is a former stray who was found on the streets of Helena, Montana. He has searched for Argentine ants on California’s Santa Cruz Island, and now he spots invasive mussels on watercraft in and around Glacier National Park.
Some dogs are searching for animals and plants that are most wanted for the opposite reason: they’re invasive species proliferating where they don’t belong and driving out native flora and fauna. There’s the previously mentioned zebra and quagga mussels, which spread by clinging to boats and watercraft, and which clog water and sewage pipes, foul up power plants, and destroy good algae. Tobias (above) is a specialist in finding them. In one test, WD4C dogs identified 100 percent of the boats with mussels aboard (human screeners spotted 75 percent). The dogs did the job more quickly, and they could also detect the mussels’ microscopic larvae.
Former shelter dog Seamus (shown at the top of the post), a border collie, is an expert in searching out dyer’s woad on Mount Sentinel in Montana.Humans have tried to eradicate the invasive weed by spotting its flowers and pulling out plants by hand, but these attempts barely made a dent. By the time it’s found, it’s often already seeded (and a single plant can produce up to 10,000 seeds). Seamus’s keen nose, along with those of three canine colleagues, learned to sniff out woad before it flowered, a time when it’s extremely hard for human eyes to see. They also found root remnants left in the ground. At a recent checkup, just 19 of the invasive plants were found on the mountain. “It will be a complete extermination,” says Parker. “It’s just going to take a long time because we don’t know how long their seeds last in the soil.”
The dogs’ hunting grounds even extend into the water. Although prized in their native habitat, brook trout are an invasive species elsewhere; in some places in the Western US, they are pushing out the native cutthroat trout. WD4C was brought to Montana by the US Fish and Wildlife Service, the US Geological Survey and the Turner Endangered Species Fund to see whether their animals could learn to sniff out live fish in moving water. Reports Parker, “This project confirmed what we long suspected: that dogs can detect and discriminate scents in water.”
Pepin can recognize 20 wildlife scents, including the scat of snow leopards, wolverines and cheetahs. In one cheetah study, he and another conservation dog located 27 scats in a 927-square-mile area. How many did humans find in the same territory? None.
Pepin (above), who worked on the brook trout project, is part of an ambitious charge to train the dogs to detect infectious diseases in animals.“He’s done the first of a lot of things for us, because he’s so game,” says Parker. Some wildlife carry brucellosis, a bacterial disease that is particularly harmful to cattle. It’s difficult to tell when animals are first infected because they typically don’t display symptoms, so in areas where the disease is prevalent, ranchers tend to keep livestock and wildlife as far away from each other as possible — severely limiting the territory and movement of both kinds of animals. The hope is that dogs could provide a fast, reliable way to identify infected herds. So far, Pepin has shown he can discriminate infected elk scat with higher and lower concentrations of the bacteria, and W4DC is eager to explore this use of dog power. “We have proof of concept,” says Parker. “I’d like to move that work forward.”
There are so many other unexplored capacities and environments where dogs could help, Parker believes. To that end, WD4C started a program in 2015 called Rescues 2the Rescue, which aims to help shelters around the world identify would-be detection dogs and place them with wildlife and conservation organizations. What kind of dogs are they looking for? Ones that are, uh, crazy.
To clarify that adjective, we’ll close by telling you about Wicket, a black Lab mix who retired from WD4C in 2017 at the top of her game, having detected 32 different wildlife scents in 18 states and seven countries. Wicket languished in a Montana shelter for six months, barking up a storm and scaring away potential owners, until WD4C cofounder Aimee Hurt found her there in 2005. When she went to adopt her, the shelter director said, “You don’t want that dog — that dog’s crazy!” To which Hurt replied, “I think she might be the right kind of crazy.”
Dr Jemsek is an Infectious Disease Doctor who played a pivotal role identifying AIDS in N. Carolina. He is my hero and Lyme Doctor.
There are several treatment methods, every doctor is different. I’m on Antibiotic IV Therapy 5 days a week, and a Lactose Ringer when not on IV Therapy, close to 30 supplements, a Morphine Patch, two horrible liquid Rx’s, and close to 35-40 prescriptions.
YouTube is an awesome source for Lyme information.
FDA MedWatch – Codeine Cough-and-Cold Medicines in Children: Drug Safety Communication – FDA Evaluating Potential Risk of Serious Side Effects 07/01/2015
Codeine Cough-and-Cold Medicines in Children: Drug Safety Communication – FDA Evaluating Potential Risk of Serious Side Effects AUDIENCE: Family Practice, Pediatrics, Surgery, Patient
ISSUE: FDA is investigating the safety of using codeine-containing medicines to treat coughs and colds in children under 18 years because of the potential for serious side effects, including slowed or difficult breathing.
Children, especially those who already have breathing problems, may be more susceptible to these serious side effects. In 2013, FDA warned against using codeine in children who recently had surgery to remove their tonsils and/or adenoids.
In April 2015, the European Medicines Agency (EMA) announced that codeine must not be used to treat cough and cold in children under 12 years, and that codeine is not recommended in children and adolescents between 12 and 18 years who have breathing problems, including those with asthma and other chronic breathing problems.
FDA will continue to evaluate this safety issue and will consider the EMA recommendations. Final conclusions and recommendations will be communicated when the FDA review is complete.
BACKGROUND: Codeine is a specific type of narcotic medicine called an opioid that is used to treat mild to moderate pain and also to reduce coughing. It is usually combined with other medications in prescription and over-the-counter (OTC) cough-and-cold medicines.
RECOMMENDATION: Parents and caregivers who notice any signs of slow or shallow breathing, difficult or noisy breathing, confusion, or unusual sleepiness in their child should stop giving their child codeine and seek medical attention immediately by taking their child to the emergency room or calling 911. Parents and caregivers should always read the product label to find out if a medicine contains codeine and talk with their child’s health care professional or a pharmacist if they have any questions or concerns. Health care professionals should continue to follow the recommendations in the drug labels and use caution when prescribing or recommending codeine-containing cough-and-cold medicines to children.
Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:
Complete and submit the report Online: http://www.fda.gov/MedWatch/report
Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
Read the MedWatch safety alert, including links to the Drug Safety Communication and previous MedWatch alerts, at:
Four months ago I wrote the last Lyme Journal Entry. I thought my strength would allow me to blog through the illness. Then the 5-6 month point turned my life upside down and it’s been hell. I fired my Lyme doctor and not taking meds at this time. I know many are wondering why the hair photo? I was losing hair by the handful and showering was nearly impossible with longer hair. When you can’t stand, lift your arms or sit down without falling, showering is a problem. I planned a nice Army shave but David would not help. I grabbed the scissors and cut eight inches off. Feels great, looks like crap. Who cares?
I’m sure people have noticed my positive attitude is quickly sliding. The mounting problems are not all Lyme-related. My cat Truffles is dying, lack of communication from my doctor, getting so sick, and walking some days is extremely painful. Our bed was too hard so I moved to a couch months ago. I live on the couch now. Not bad for sleeping except all the animals want to go out, poke me in the back, and the cat wants to attack me. Even attempting to get enough sleep is impossible. With Chronic Lyme Disease sleep is your best friend and a key to survival.
Let me share some Lyme politics for newbies.
Most of the expert Lyme Literate Doctors, are not practicing. Several years ago doctors were watching people die using CDC standards, which state patients can only receive 2-4 weeks of antibiotics at most. The Lyme doctors who understood how the viruses worked knew 4 weeks was a joke. The doctors worked together helping each out calling in antibiotics for the other patients. I have Chronic Lyme, and it can take 1-3 years to get well. Medication is one of the many ways to heal. Getting enough sleep is number one after the meds., take supplements, gluten-free diet and eat foods to help your body heal. No Coffee and drink only electrolyte water.
There was a huge division among Lyme doctors when the CDC allowed several doctors to patent the virus. Makes no sense to me. For years patients were clueless of the division. Both sides fought hard with the CDC to prove their data, from the videos on YouTube it looks like the battle was lost before the presentations started. The expert Lyme Literate doctors were quite vocal and a witch hunt is what followed the meeting. Doctors appeared before the Medical Board and were not able to practice, some for up to a year. Several doctors lost their clinic and everything they owned trying to keep their patients alive. It is a complete mess the CDC let happen, needless to say, I’m pissed. Just a little more background info to burn into your brain.
Many Chronic Lyme patients become so sick they are not able to work. The first reality is you no longer have insurance and can not afford new insurance if you could buy. I’ve watched video after video on YouTube of people with good-paying jobs, racking up several thousand dollars in doctor bills and many having to file bankruptcy, losing everything. One video told of a couple who owed their parents $500,000. Lyme affects everyone in your family, friends, your health, and financial security.
It’s going on Spring in some parts but summer will be here quickly. I don’t want any of you or your family members to struggle with a virus that looks like a worm. The viruses travel through the blood until they can find a way to your major organs. Lyme likes to get cozy in the liver, kidney, heart, and brain. I have three tick-borne illnesses and Epstein Bar Virus. I have cognitive issues, my eyes constantly see things moving by my peripheral vision and balance are fleeting. I was in the bathroom two days ago about to reach for the medicine cabinet. I slammed into a wall hurting my writs and several fingers. If that wasn’t enough I slid down the wall falling on the toilet and hurt my leg. The doctors don’t know how much of your ability will come back if any. You have to keep fighting.
Why I fired my doctor. My husband and I formed an impression at the first appointment, not so good. I was desperate to start treatment and had no other options.
* I start a couple of drugs until the Lab work is back. At the follow-up appointment, the first words out of his mouth are you are in a great deal of pain. REALLY? His communication and organization skills are lacking. No pain meds were prescribed. He has to call someone in to bring him something several times during the appointment.
*I’m loaded down with over 50 pills to take a day plus 15-20 supplements and sleep all I can. The equation doesn’t work. I have gastro issues and the high-powered antibiotics made me nauseous all the time. I asked to have a PICC line in my arm to give my stomach a break. He did not plan to use a PICC line? Almost every patient gets a PICC line so they can fill you full of drugs and bypass your stomach. My wheels are turning. He had lab work for me to do, but I didn’t do it. He never asked about the Labs. He said my Lead levels were three times higher than normal, in the dangerous range. No follow-up test was ordered, it was like “So you know”. I’m scared, my brain is on overload, the test said current and ongoing exposure. I spent about two weeks looking for an answer. I looked at the top of the report one day, it wasn’t my report. Admin acted like no big deal. HIPPA laws are not new.
With the list of experts I start going down the list, ONE of the leading Lyme Literate Doctors still practices. The doctors called before the Medical Board and CDC. Now are full-time advocates/researchers. I phoned his office in DC and they are taking patients. When you have cognitive issues filling out 50 pages is crazy. I stayed up last night to get everything I could without waking my household. With God’s help, I will finish the paperwork tomorrow and get an appointment in the next month.
ILADS is the professional organization Lyme Literate doctors belong to. I saw the tab on site for ILADS Protocol on Lyme. I jumped for joy. Let’s hit them with our best shot. We have boxing gloves on and the truth will come out. The document was extensive for the different stages of Lyme or other tick-borne illnesses. I felt so happy that others may not have to suffer shortly. The document was well-researched by leading scientists, leading hospitals, and large populations of people. I cheered when I read research that outlined how the current system is incorrect, and they went all out. On the issues of insurance, extensive research with real patients exposed what the CDC is keeping from the public. If you want to learn more about Lyme, YouTube has so many videos, you might not have to go anywhere else. If you like the medical jargon go to the ILADS site.
A shout out to others who suffer from Lyme or tick-borne illness. I think of you, pray for you, and send good karma your way.
It’s interesting the events our mind suppresses or forgets. I have no problem or emotion talking about the physical and emotional abuse at the hands of my mother and step father. I have disassociated memories of sexual abuse by my father. I know it. My therapist and I have talked about it, she doesn’t push and knows if the door opens I’ll talk. What I will not do is force my mind and body to endure pain it’s not ready for. I have a good perspective on what I’ve survived and the methods our mind uses to deal with our deepest pain. I’m not sure if this particular memory was forgotten or suppressed. I had no emotion as my therapist was almost brought to tears.
I saw a story on the news about a 8-year-old girl tortured by her parents in some way. I don’t recall the circumstances. I always plan what I want to talk about but this day was different. I sat down and the memory of the little girl crossed my mind. I asked her if she had heard the story then adding my thoughts. I started to cry which I do easily for others in pain. As we talked about what type of parent would do that, a childhood memory flooded over me. The tears dried and it was if I was talking about someone else. When I was 8 years old I started having terrible side pains and daycare called my mother. She didn’t take off early and it was maybe 3 hours before she arrived. At that point I could barely walk and could not walk and breath. The supervisor thought I had an appendicitis attack and should get to the hospital right away. It was Halloween night and I didn’t want to miss out on the candy but pain was taking over my small body. My mother was angry for ruining things for my brother, nothing new about that. I guess we did not have insurance since the first hospital turned us away. We are talking early 1970’s. She drove to the county hospital and I waited on a bed until the people bleeding and dying received treatment. Halloween night is one of the busiest nights of the year with more shootings than normal. The emergency room was full and I was outside a mans curtain to wait my turn. During this time my mother left to take my brother to trick or treat. I didn’t realize until a nurse asked where she was. I said she talked to a nurse and went home. She was a big woman and I knew nobody gave her any shit. Asking why in the hell my mother would leave me there. My answer did not sit well with her, I knew a beating was in store for me. One thing to keep in mind is the county hospital is in the hood in one of the worst areas of Dallas. This is not a place an adult would feel comfortable let alone a child. I was on my side crying in pain and saw the man thru the curtain. He was an older man and he had what looked like wires coming out of several places on both arms. My eyes caught his, I ask does that hurt. He was a kind man saying not as bad as my pain did and then where was my mother. I told him how upset I was that my brother would not share his candy with me. He looked shocked my mother would leave me there. My mother eventually came back in the greatest of moods and was raising her voice at the big nurse. I was rooting for her to punch my mother if the mouth or grab her by the neck. I have no doubt it happened many times getting drunks under control.
The doctor didn’t think I needed surgery, just to stay overnight for observation. For a second I was glad until rolled to my room. The hospital was so overcrowded I hade to sleep in a baby bed. That is the last thing a kid (big girl) wants to hear. I cram myself in the bed and they pull the side up. It was so dark in there I thought I was alone until babies started crying. Which made it much worse for me. Not only did I have to sleep with my legs pulled up, babies are crying and my mother is home in her comfortable bed.
You would think at this point in the story I would feel some emotion but my mind switches back to the little girl. My mind turned a switch, my story was over, no big deal, that was my mother, that was my life. I couldn’t help but cry for the other girl. How can people do that to their children. As I’m talking to my therapist my story and pain never crosses my mind again. That was several years ago, it buried itself and popped back up last week.