Is your doctor hiding something from you? It’s possible! Many doctors are bullied by other doctors into keeping silent about what REALLY goes on behind closed doors. This is a video you have to see to believe!
Do you have a #bullydoctor? You’re not alone! Share your story anonymously, and get the word out about medical mistreatment of patients with chronic pain.
Prevent An Ostomy With This Incredible Ulcerative Colitis Cure!
An inspiring interview with Kristin Thomas of ThriveByFood.com
I’m fairly certain that if I hadn’t been diagnosed with gluten intolerance in 2002, I would have ended up having parts of my colon removed and/or be living with an ostomy bag by now. My digestive issues were horrific and had been since birth.
So, whenever I hear someone (besides me) who has an inspiring story about how food and dietary changes have put their life-threatening conditions into remission, I can’t wait to interview them and share their story with the world.
This is my interview with Kristin Thomas of www.ThriveByFood.com, who is living proof that risky surgery can be avoided and ulcerative colitis can go into complete remission within two short weeks!
No Matter How Well She Ate, Kristin Was Starving
I asked Kristin what kind of symptoms she experienced due to her ulcerative colitis.
This was her response:
Throughout the years when my ulcerative colitis was flaring, I experienced it all:
- Sharp abdominal pain
- Intense bloating
- Gas and belching
- Abnormal bowel movements
- Extreme fatigue
The fatigue and poor sleep aspect I never connected to my ulcerative colitis, but now with my background in functional medicine and nutrition, I understand it was certainly part of it.
My body wasn’t able to break down and absorb the nutrients from my food, as healthy as it was, which was depriving my body of the key vitamins and minerals it needed to energize and fuel me, as well as give me a restful night’s sleep.
Baffling Symptoms That Appeared Out of Nowhere!
When it comes to ulcerative colitis and other chronic digestive diseases, symptoms usually begin in the teens or early 20s. This was the case with Kristin, as well.
In Kristin’s words:
The first digestive symptoms I experienced were in my late teens. It started as acid reflux and lactose intolerance. Within just a few years time, though, it progressed to full-blown ulcerative colitis. Year after year, my symptoms got worse and worse, well beyond daily acid reflux to almost debilitating pain and brain fog.
The Road to a Diagnosis
Kristin was one of the lucky ones. It only took a year for her to receive an official diagnosis of chronic ulcerative colitis.
As Kristin put it:
For many years prior to that, though, the only “diagnosis” I got was IBD, but this felt too broad of an answer, so I wanted to dig deeper.
At the time, when my symptoms were really escalating out of control, I went to every major doctor and hospital in Boston, MA (where I was living at the time) to find answers, and, after far too many tests, they finally determined it was chronic ulcerative colitis.
Doctors Flat-Out Dismissed the Idea of Leaky Gut and Candida
When I asked Kristin if doctors said that her symptoms were “all in her head”, she revealed that her medical team took her seriously at first, running the right tests to get to the bottom of them.
However, her doctors began to give her funny looks when she went to them with some research she’d done on her own.
It was at the point after my ulcerative colitis diagnosis when I started learning about issues like leaky gut, candida, and parasites that my doctors began dismissing me.
They refused to run these tests on me, so, it was at that point that I turned to find other options.
Desperate Times Call for Desperate Measures
I asked Kristin when she started to use food to heal her ulcerative colitis, and that’s when she revealed the frightening words her medical team dropped on her:
[I started thinking about using food to heal my UC] at the point where the only solution my medical team had for my worsening ulcerative colitis was surgery and an ostomy bag.
I knew that wasn’t the right answer for me. In fact, I saw it as a Band-Aid to cover up the fact that they didn’t know how else to dig into the root of my issue.
So, I began researching holistic healing paths I could take. I first began seeing an acupuncturist who immediately asked me about my diet, something no doctor had ever asked me about.
While I generally ate healthily, there were foods like wheat, sugar, and soy in my diet that she explained were very inflammatory, especially to those with compromised digestive function, and she directed me to a diet plan that was whole, clean, and anti-inflammatory.
Just Two Weeks to Better Health
Faced with very difficult choices, Kristin decided to put this new nutrition information to immediate use.
In her own words:
At this point, I was willing to try ANYTHING because I had been at the worst of the worst with this disease, it felt. I had no idea just how powerful a change in my diet would truly be, though.
Within two weeks, I started to notice huge improvements. I no longer woke up with stabbing pains or experienced bloating after every meal. My bowel movements normalized, and even my energy levels spiked.
This was amazing! My body was responding so incredibly well to these dietary changes that I kept researching more about it and continued to find ways to use food as medicine.
By cutting out foods that were irritating my gut, and loading up on foods that would heal and nourish my gut, I was able to calm down the inflammation, eliminate the triggers of many of my symptoms, and put my body at ease.
For the first time in years, I finally felt normal.
Changing Your Diet CAN Put Chronic Illness Into Remission
One of the most common reasons people with autoimmune disease and digestive disorders do not attempt to change their diets is the belief that doing so will not make a difference.
But, it DOES work! Making dietary changes has saved thousands of lives, including mine and Kristin’s.
Here’s her recommendation:
The food you put in your body has an immense impact on how you feel.
After all, food is fuel, it has been since the very start of humankind, so if we are not consuming the right foods, our bodies will not be healthy. Every bite you eat is either feeding into disease or working to heal you, and I encourage you to allow your body to heal.
It’s the single best thing I did for my body, and continue to do today. Simply by removing trigger foods like gluten, dairy, soy, and sugar, you will notice a difference.
I encourage everyone to do this for 30 days and simply notice the changes within. It’s incredible how willing the body is to return back to baseline with the right nourishment.
I agree, and I’m so thankful for people like Kristin and others who have shared their amazing stories, proving that there is still hope for a better life for those living with chronic illness.
Learn more about Kristin and how YOU can achieve full remission of your chronic illness by visiting www.ThriveByFood.com!
Need more proof dietary changes can put your chronic illness into remission? Check out these articles!
Not sure how to eat a gluten-free diet? No problem! I created a 5-part guide just for you. Click on the link below to get started!
Have you ever felt so confused, so helpless, and so filled with terror that you just checked out? I did. This is how I found my way back home.
Article originally published by The Best Years In Life
Do you live with chronic allergies, unexplained pain, and debilitating fatigue? Millions struggle with mystery symptoms their doctors can make no sense of. If you’re one of them, toxic mold could be the hidden cause!
The most common types of mold include:
- Stachybotrys chartarum and Stachybotrys chlorohalonata (Black molds)
Black molds are the most dangerous to your health and are commonly found in water-damaged areas of buildings and in wet basements. Black molds contain neurotoxins that have been linked to serious, long-term neurological dysfunction.
In this article, I will show you the most common symptoms of mold sensitivity. In the second article, I will show you where to find mold lurking in your home. In the last article, I will show you how to get rid of toxic mold naturally.
Let’s get started by looking at the 10 most common symptoms of mold sensitivity:
1. Numbness and tingling
The neurotoxins produced by mold can cause numbness and tingling in your extremities. If you’ve ever had a foot “fall asleep” due to sitting on it wrong, you know how strange and uncomfortable it feels when the blood rushes back. If you’re being affected by toxic mold, the numbness and tingling you’re feeling could be a warning sign of neurological damage.
Research shows that individuals with chronic toxic mold exposure are vulnerable to vitamin B12 deficiency. Your body needs vitamin B12 to make DNA, nerves, and blood cells. If your body does not have enough of this critical nutrient, it can cause serious neurological and mental impairment.
According to a case report published in the French journal, Encephale, patients with vitamin B12 deficiency can show signs of depression, mania, and psychosis.
2. Upper respiratory problems
If you’re prone to sinus infections, excessive mucus in your throat, have a dry and hacking cough, or experience tightness in your chest, you may have an allergy to mold.
According to the CDC, the Institute of Medicine (IOM) found evidence that indoor mold exposure can cause upper respiratory problems for those susceptible to asthma. Exposure to mold has also been linked to respiratory illness in otherwise healthy children.
3. Learning and memory problems
Brain fog, memory problems, and difficulty concentrating are so common, many chalk these symptoms up to stress, lack of sleep, or age. However, they could also be a sign of toxic mold exposure.
In a 2003 study conducted by the Environmental Health Center-Dallas, nervous system challenges were observed in every single study participant exposed to mold. That’s 100 out of 100. A significant portion of the participants who were exposed to mold also presented with abnormalities in their brain SPECT scans.
4. Blurry vision
When black mold mycotoxins come into contact with your eyes, they kill the cells within, which can lead to inflammation, injury, and vision problems.
5. Light sensitivity
Light sensitivity, also known as ‘photophobia’, is linked to a malfunction of the nervous system.
Warning: If any of your senses are more sensitive than you’re used to (lights are too bright, sound is too loud, touch is irritating), it could be a sign that toxic mold is slowly destroying your nervous system!
6. Autoimmune disease
If you’ve been diagnosed with any type of autoimmune disease, it is critical that you check your home and work surroundings for mold. According to the American Medical Association Journal of Ethics, molds and mycotoxins have been linked to the development of chronic fatigue syndrome and fibromyalgia.
7. Recurring headaches
If you’re sensitive to mold, your sinuses can become chronically inflamed and congested, leading to recurring headaches that concentrate in the forehead and below the eyes.
Furthermore, toxic mold may be what’s causing your migraine headaches. Research suggests that immune system cells sensitive to mold will release chemicals that cause the blood vessels in your head to swell, triggering a migraine.
8. Skin rash
Recurrent skin rash is another telltale sign of mold sensitivity. When you come into physical contact with mold, you develop histamine bodies as a defense mechanism.
The most common way this occurs is during yard work when you’re exposed to wet leaves and dirt. The rash usually originates at the point of contact and spreads from there.
9. Muscle and joint pain
Research shows that the joint pain caused by long-term mold exposure is nearly identical to the pain caused by rheumatoid arthritis or fibromyalgia. This can lead to a misdiagnosis and a prescription for painkillers.
As long as you remain in the mold-contaminated environment, your muscle and joint pain will persist. Meanwhile, your body will build up a tolerance to pain medication and, over time, the drugs won’t work as well.
Plus, the source of the problem is still right there, lurking silently in your environment, making you sicker and weaker by the day.
There are dozens of reasons you might feel exhausted all the time. One of them is long-term toxic mold exposure. If you inhale and/or come into contact with mold on a regular basis, your immune system will be in a constant state of “fight or flight”.
Over time, this non-stop immune system response can lead to autoimmune disease and chronic fatigue.
If sensitivity to mold is what’s causing your mystery symptoms, you’re actually in luck. Now, all we have to do to get your health back on track is figure out where it is and get rid of it!
Head on over to The Best Years In Life to read the second and third articles in this 3-part series.
“I have a chronic illness. Now what?”
I’ve been spending a ton of time on Instagram lately, connecting with the amazing spoonie community there. I often ask questions to increase engagement, and I’ve found a veritable treasure trove of information that I can’t wait to share with you every week!
A few months ago, I asked the question:
“What’s one piece of advice you would give to a new spoonie?”
Below are the helpful, well-thought-out answers I received.
1. Allow yourself to mourn your former life.
One of the most important things you can do early on in your diagnosis is take the time to mourn your former life.
Learning that you have a chronic illness and that you may not be able to accomplish the same goals you set for yourself years ago can be as startling and painful as learning of a sudden death.
Like mourning the loss of a loved one, you will go through the usual grieving stages:
You don’t have to go through this process alone. There are support groups online and in person that can help. You might also consider talking with a professional therapist during this critical time.
2. Connect with other people living with similar chronic illnesses.
If you don’t know it yet, there is a huge, and I mean HUGE chronic illness community online. Just type the word ‘spoonie’ into any search engine or look up the hashtag #spoonie on social media accounts.
Making connections with those who are living with similar chronic illnesses offers you a deeper level of support than you can get from someone in perfect health, no matter how well-intended that person may be.
3. Change your mindset and make new goals surrounding that mindset.
Another important thing to remember as a newly diagnosed spoonie is that there will be a new normal to adjust to. Remember, this is not an end to your life, this is a detour. This means you can still accomplish goals and fulfill your heart’s desires, you’ll just have to blaze a new trail to those goals and desires.
4. Keep track of physical and emotional changes via journal or app.
Fatigue, brain fog, and pain can make it difficult to keep a mental note of how you feel on a daily basis. Keep a journal or download an app to keep track of your flares, food triggers, emotions, etc.
As you get to know your body, you’ll have a better idea of what makes you feel better, what makes you feel worse, when you have bursts of energy, and when you need to take a nap!
I highly recommend Daylio. It’s a free app that I’ve been using for months, and, with my incredibly poor memory, it’s been invaluable to me.
5. Don’t push your friends and family away.
It’s very common for newly-diagnosed spoonies to push everyone away. I completely understand. I did the exact same thing. As a matter of fact, I still do. I isolate to keep my stability, deal with sensory overload (I’m on the autism spectrum), and “protect” others from the symptoms of my chronic illnesses when they get particularly bad.
To me, it’s as natural as breathing, so to advise you not to push your friends and family away goes against my own natural instincts. However, it’s very good advice that was given to me by one of my amazing linewalkers on Instagram.
True, friends and family may not fully understand what you’re going through or how you’re feeling, but they are your biggest supporters. Plus, and this is an important one, the more time you spend with them, the more likely there are to feel connected to you and become familiar with the symptoms of your illness.
It’s more difficult for someone to claim you’re “making it up” when they physically see what you’re going through on a regular basis.
6. Learn to say “No” without explaining yourself.
“No” is the most important word a person with a chronic illness can use. If you’re the type who is accustomed to taking on too much, it may be very difficult to delegate tasks, trust others, and say “no” to those you care about.
In the long run, though, saying “yes” to all the things you used to will only bite you in the butt, because you might not be able to complete the task as requested (or even remember to do it), and then you’ll feel guilty, exhausted, and maybe even resentful towards the people who asked.
You don’t have to explain yourself all the time, either. A simple, “I’m sorry, I can’t do that” should suffice.
People may be irritated or offended at first, but if they know you have a chronic illness and they know you as a person, they’ll adjust.
7. Research your own chronic illness.
I can’t stress this one enough. Research your own illness! Dealing with the conventional medical community can be like navigating a minefield. You have to be informed and on guard.
Most conventional doctors are not taught nutrition and the mind-body connection. They also have a rather horrible habit of downplaying symptoms in patients with chronic illness, especially women.
So, stay up to date, be informed, and be your own best advocate!
Also, if you ever have a doctor that takes issue with you doing your own research, find another doctor. That’s a sign of egotism on their part, and that’s the last thing you need when you’re at your most vulnerable.
8. Be more mindful and in the moment.
Your life has changed, and, while that can be difficult to adjust to, it will be easier to handle if you stay mindful and live in the moment.
For example, instead of trying to figure out how you’re going to have the energy to go to a wedding in three months, focus your attention on just the next three days.
If necessary, the next three hours or three minutes, even. Breaking life down into bite-sized chunks is an excellent way to reduce anxiety and feelings of overwhelm.
Also, instead of thinking, “When I get better, I will…” say, “On a day I feel better, I will…”
This small change in your thinking can help you feel more motivated and positive.
9. Rest and pace yourself even when it’s hard.
Ah, pacing. What’s that? If you’re anything like me, you go and go and go until you burn out and end up in bed for days. Unless you’re on an actual deadline, force yourself to take breaks in between activities.
- Work on a project, take a break (rest, meditate, nap, watch a movie), and then go back to your project.
- Buy your groceries one day, cook the next.
- Write an article in the morning, edit it at night.
10. Appreciate the little things.
When you’re living in a 9 to 5 world, trying to balance career, family, and a social life, it can be hard to remember to appreciate the little things.
This is one of the unexpected advantages of living with a chronic illness: You have now transitioned from a typical human pace to nature’s pace.
Raindrops, flowers, insects, squirrels, the scent of a candle, the feel of your pet’s fur, and the delicious warmth of sinking into a hot bath—Those are all yours now, and they are all precious.
11. Put yourself first.
When you’re newly diagnosed with a chronic illness, it can be very difficult to put yourself first, especially if you’re not used to it.
Remember, your abilities have changed. Expecting that you’ll be able to go at the same pace you used to, helping everyone with everything, and taking on task after task is not only unrealistic, it’s bad for your health.
Put yourself first. It may sound selfish, but it isn’t. Recharging your own batteries so that you have enough energy for yourself and others is one of the best things you can do for yourself and those who count on you.
12. Have an advocate by your side.
Whenever possible, take another person with you as an advocate and support. Medical staff are far less likely to be dismissive or take advantage of their patients when there’s someone else around.
I know this sounds scary, but some doctors are complete and total jerks. You need to be aware of this and protect yourself whenever necessary.
These are some of the things I wish I’d known when I was diagnosed in my early 20s. It would have saved me a LOT of grief!
What about you? What advice would you give to someone who is newly diagnosed with a chronic illness? What is the best advice you’ve received?
Share in the comments below!
Have you ever heard a doctor say “You’re making it up” or “It can’t be that bad!” Women with chronic pain have a very hard time being taken seriously by doctors. Here are 5 frustrating and heartbreaking stories.