Dr. Wallach’s Cystic Fibrosis Cure

Interview

Joe: Dr. Wallach — I have a question for you: my wife Nelly has cystic fibrosis. You say nutrients can fix disease. What should she do? What is your “90 for Life” program and exactly how much selenium should she take?

Dr. Joel Wallach (paraphrased, summarised): My core idea has always been that the body needs a set of essential nutrients every day — a set I call the “90 essential nutrients” (vitamins, minerals, amino acids and essential fatty acids). The “90 for Life” concept (and the product lines built around it) are designed to supply those nutrients every day in a supplement program. Youngevity and related distributors sell multi-product packs that aim to deliver the 90 essentials. Youngevity+1

Joe: Specifically about selenium and CF: how much do you recommend?

Dr. Wallach (paraphrase): I recommend correcting documented deficiencies. Many people with chronic disease can be low in trace elements; the plan is to restore normal blood levels with targeted supplementation. For a person with malabsorption (common in CF), that often means more than the general RDA — but it should be measured and monitored. (Note: different providers and product labels vary; I advise checking serum selenium or glutathione peroxidase activity and working with a clinician to decide a safe dose.) The Wallach Revolution+1


Joseph C. Jukic:
Dr. Wallach, you’ve been saying for decades that cystic fibrosis is not a genetic disease but a nutritional deficiency. Could you share an anecdotal story—a real case—where someone actually reversed cystic fibrosis using your 90 for Life program?


Dr. Joel Wallach:
Absolutely, Joe. I’ve seen this many times, but one story stands out. Years ago, there was a young boy, about six years old, diagnosed with cystic fibrosis. His parents were told by the medical doctors that it was incurable—that he’d be lucky to live past his teens. They were desperate, but they found my lectures and decided to try my nutritional program.

We started him on the 90 essential nutrients—that’s the 60 minerals, 16 vitamins, 12 amino acids, and 3 essential fatty acids—and I emphasized extra selenium because that’s the key mineral involved in the pancreatic and lung tissue repair. He was getting about 200 micrograms per 25 pounds of body weight, spread throughout the day.

Within three months, his coughing reduced dramatically. The mucus production dropped. Within a year, the doctors were puzzled because his lung function was nearly normal, and he had gained weight for the first time in years.

I remember the mother calling me crying, saying, “Dr. Wallach, they told me this was impossible.” And I said, “No, ma’am—it’s only impossible if you believe the disease is genetic. It’s a nutritional deficiency problem.”

We ran similar protocols with other children, and we got the same results—every single time, Joe. The pancreas, lungs, and intestines healed themselves once the body got what it was missing.


Joseph C. Jukic:
That’s incredible. So the turnaround began when you focused on selenium and the full 90 nutrients?


Dr. Joel Wallach:
Exactly. Selenium, zinc, calcium, magnesium—all the cofactors have to be there. You can’t just throw one nutrient at it. The human body is like an orchestra—if one section is missing, the music doesn’t sound right. But when you give it all 90, it can play the symphony of life again.

And that’s why I say—there are no genetically transmitted diseases. Only nutritionally transmitted ones.

Joseph C. Jukic:
Dr. Wallach, can you break down exactly what that young cystic fibrosis patient took—the supplement names, the dosages, and what foods you had him eat or avoid?


Dr. Joel Wallach:
Sure, Joe. Let’s get specific. When I work with cystic fibrosis cases, I always start with my basic foundation—the “90 for Life” program. That means every day, the person must get:

  • 60 essential minerals
  • 16 vitamins
  • 12 amino acids
  • 3 essential fatty acids

That’s the baseline. Without all 90, the body can’t maintain or repair tissue properly.

Now, here’s what that looks like in practice:


💊 Supplement Protocol (Dr. Wallach’s Typical CF Program)

  1. Healthy Start Pak (or Healthy Body Pack 2.0)
    • Provides the 90 essential nutrients.
    • 1 pack per 100 lbs of body weight, divided into 2 servings daily (morning and evening).
    • Contains:
      • Beyond Tangy Tangerine (BTT) – full-spectrum multivitamin-mineral complex.
      • Osteo FX Plus – calcium, magnesium, and vitamin D3 blend for connective and bone health.
      • EFA Plus – omega-3, -6, and -9 essential fatty acids.
  2. Selenium (Ultimate Selenium)
    • The key nutrient for cystic fibrosis.
    • 200 micrograms per 25 pounds of body weight daily, divided into two or three doses.
    • So if the child weighs 75 lbs, that’s about 600 micrograms per day (3 capsules).
    • Selenium is vital for the pancreas and lung tissue—it protects against oxidative damage and supports enzyme production.
  3. Ultimate Enzymes (Digestive Support)
    • 1–2 capsules with each meal.
    • Helps with fat absorption and reduces digestive stress—crucial for CF patients who have poor pancreatic enzyme output.
  4. Ultimate Flora FX or Probiotic Plus
    • 1 capsule twice a day to restore gut flora balance.
    • A healthy microbiome improves nutrient absorption and immune defense.
  5. Z-Radical (Fucoidan & Seaweed Blend)
    • 1–2 ounces daily.
    • Helps repair damaged lung tissue and boosts immunity.
  6. Beyond OsteoFX (Liquid Calcium-Magnesium)
    • 1 oz twice a day to support bone strength and reduce inflammation.

🥗 Dietary Recommendations

Foods to Eat:

  • Free-range organic eggs (soft-boiled or poached, not fried) – for protein and healthy fats.
  • Grass-fed butter and ghee – for natural fat-soluble vitamins.
  • Avocado, coconut oil, and olive oil – healthy oils for cell membranes.
  • Bone broth, liver, and organ meats – high in minerals and natural enzymes.
  • Wild-caught salmon, sardines, and shellfish – rich in selenium and omega-3s.
  • Fermented foods – like sauerkraut and kefir, to strengthen gut health.
  • Gluten-free grains – rice, quinoa, buckwheat.

🚫 Foods to Avoid Completely

(Dr. Wallach is strict about this.)

  • No gluten – wheat, barley, rye, oats (destroys intestinal villi and blocks absorption).
  • No fried foods – causes oxidative stress and destroys nutrients.
  • No processed meats – bacon, hot dogs, deli meats (contain nitrates/nitrites).
  • No oils – especially canola, soy, corn, sunflower, and grapeseed oil.
  • No carbonated drinks – they neutralize stomach acid, blocking mineral absorption.
  • No sugar or soda – suppresses immune function and feeds infection.

Dr. Wallach (continuing):
Within a few weeks of that strict program, the parents usually notice the mucus loosening up, the cough reducing, and the child sleeping better. After about 90 days, they see a transformation—better energy, normal bowel function, weight gain, and improved breathing.

I’ve seen it over and over again. The key is consistency—you can’t cheat on the diet, and you can’t skip supplements. Once the body gets the 90 nutrients consistently, it can rebuild itself—lungs, pancreas, everything.


Joseph C. Jukic:
That’s powerful. So, in your experience, cystic fibrosis can be completely reversed if someone stays disciplined on the 90 for Life plan?


Dr. Joel Wallach:
That’s right, Joe. In every case I’ve seen where people followed it exactly, they got better—sometimes dramatically. The human body wants to heal. You just have to feed it what it needs and stop poisoning it.

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The Breath of Courage

Nelly Furtado sat in the sterile, white-walled clinic, her hands gripping the edges of her chair. The faint hum of fluorescent lights above her felt deafening. Her chest tightened—not from the cystic fibrosis that had plagued her for years, but from the overwhelming anxiety that came with being in a doctor’s office.

The door creaked open, and Dr. Fishbein walked in, his lab coat slightly askew and his clipboard balanced precariously in one hand. His round glasses magnified his eyes, giving him an almost cartoonish appearance.

“Nelly,” he began, his voice nasal but oddly cheerful, “we’ve reviewed your latest tests. Your lung function has declined significantly. It’s time we seriously consider a lung transplant.”

Nelly’s breath hitched, and she shook her head vehemently. “No,” she said, her voice trembling. “I—I can’t. I don’t want to go through that.”

Dr. Fishbein set the clipboard down with a theatrical sigh, clasping his hands together as though preparing for a monologue. “I understand this is overwhelming, but this could give you a new lease on life! Without it, well… let’s just say things won’t improve.”

Nelly’s heart raced. The thought of surgery—of doctors poking and prodding, of tubes and machines—was unbearable. She had always hated hospitals, their antiseptic smell and cold, impersonal atmosphere. They reminded her of fragility, of mortality.

“I can’t,” she repeated, tears welling in her eyes. “I just… I can’t.”

Dr. Fishbein leaned in, his tone suddenly conspiratorial. “Look, I know it’s scary, but think of it as a grand adventure! You’ll be the phoenix rising from the ashes! Take your time to decide, but remember, the clock is ticking.”

Later that evening, Nelly sat on her couch, staring out the window at the city lights. Her mind raced with fear and doubt. Would she even survive the surgery? What if it didn’t work? The idea of trusting her life to doctors and machines felt impossible.

A knock on the door broke her spiral of thoughts. It was Joe. He had always been her rock, her steady hand in the storm.

“Hey,” he said, stepping inside. “You doing okay?”

She shook her head, her voice barely a whisper. “They want me to get a lung transplant.”

Joe sat beside her, his expression thoughtful. “That’s a big decision.”

“I’m terrified,” she admitted. “I don’t trust doctors. I don’t trust… any of it.”

Joe took her hand, his grip warm and reassuring. “You don’t have to do this alone, you know. I’ll be with you every step of the way.”

Nelly looked at him, her eyes filled with uncertainty. “What if it doesn’t work? What if I don’t make it?”

Joe’s gaze was steady. “What if it does work? What if this gives you the chance to sing again, to breathe without pain, to live?”

She closed her eyes, letting his words sink in. She thought about all the songs she hadn’t written yet, the places she hadn’t seen, the moments she hadn’t lived.

After a moment, Joe added, “But hey, before we even get to the transplant, there’s something else we could try. Have you thought about changing your diet?”

Nelly opened her eyes, frowning. “What do you mean?”

Joe hesitated, then said, “Dr. Fishbein’s diet for cystic fibrosis. Remember? The one that’s all about dairy—cheese, milk, cream, milkshakes, and cheeseburgers. I mean, come on, doesn’t that sound like something out of a bad comedy?”

She blinked at him. “That’s… the exact opposite of what I need.”

“Exactly,” Joe said, shaking his head. “And have you looked at the guy? He looks like a quack to me. You know he’s a clown school dropout, right?”

Nelly let out a disbelieving laugh. “A clown school dropout? You’re kidding.”

“Nope,” Joe said, grinning. “He couldn’t juggle, and apparently, his balloon animals were terrifying. So, he became a doctor instead, and now he’s pushing milkshakes and cheeseburgers for cystic fibrosis patients. Makes total sense, right?”

Nelly shook her head, a reluctant smile tugging at her lips. “That’s… absurd.”

Joe smiled softly. “Look, I’m not a doctor, but what if you tried cutting out dairy for a while? Just to see if it helps. I know you love cheese and ice cream, but if it makes a difference in how you feel, isn’t it worth it?”

She sighed, running a hand through her hair. “I guess I could try. But it feels like one more thing to give up, you know?”

“I get it,” Joe said. “But maybe it’s not about giving up. Maybe it’s about making space—for the things that really matter. Like your voice. Your health. Your life.”

Taking a deep breath—shallow and labored, but hers—she opened her eyes. “I’m scared, Joe.”

“I know,” he said. “But courage isn’t about not being scared. It’s about doing what you need to do, even when you are.”

For the first time that day, Nelly felt a flicker of hope. Maybe she could face this. Maybe she could trust the doctors, the process, herself.

And maybe, just maybe, she could find a way to breathe freely again.

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Jack & Jill: Us Against the World

In 2008, Jack and Jill vs. the World was released as a romantic comedy-drama directed by Vanessa Parise. It starred Freddie Prinze Jr. as Jack, a successful advertising executive, and Taryn Manning as Jill, a free-spirited woman with cystic fibrosis. Here’s an overview of the movie:

Plot Summary

Jack and Jill vs. the World follows Jack, a New York advertising executive who lives a highly structured and conventional life. When he meets Jill, she brings a refreshing spontaneity to his routine, inspiring him to re-evaluate his life. Jill has cystic fibrosis, which she initially keeps hidden from Jack. As their relationship deepens, she reveals her condition, and the two begin to navigate the complexities of loving and supporting each other while dealing with the realities of her illness.

The movie mixes humor with romance and drama, exploring themes of freedom, love, acceptance, and the idea of living life to the fullest in the face of life’s uncertainties.

Key Themes and Reception

Jack and Jill vs. the World emphasizes “living for today” and challenging the expectations of society. The film received mixed reviews, with critics generally appreciating the chemistry between the lead characters and the film’s focus on cystic fibrosis, though some found the story predictable.

Impact and Representation of Cystic Fibrosis

The film helped bring cystic fibrosis into the spotlight, portraying both the physical and emotional challenges of the condition while celebrating a character who seeks to live fully despite it.

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