Is there anything to help stop or slow progression of MGUS?

Posted by amyboylan1 @amyboylan1, Oct 12 10:14pm

I am wondering if there is anything anyone is doing to stop or slow the progression of MGUS. I m recently diagnosed and have a lot to learn. My oncologist said there is nothing that can be done. Also could some of you share how long you have had MGUS. I am like I’m sure like all of you very concerned about my MGUS processing. Thank you.

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### **Risk Stratification in MGUS: Low, Intermediate, and High Risk**

MGUS (Monoclonal Gammopathy of Undetermined Significance) is stratified into risk categories to estimate the likelihood of progression to **multiple myeloma (MM)** or related disorders. The risk assessment considers clinical and laboratory factors.

---

### **Key Factors for Risk Stratification:**
1. **M Protein Level (Monoclonal Protein)**
- **Low Risk:** < 1.5 g/dL
- **Intermediate/High Risk:** ≥1.5 g/dL

2. **Type of M Protein:**
- **IgG:** Lower risk compared to IgA or IgM.
- **IgA or IgM:** Higher risk.

3. **Free Light Chain (FLC) Ratio:**
- **Normal Ratio:** 0.26 – 1.65
- **Abnormal Ratio:** Outside this range indicates higher risk.

4. **Bone Marrow Plasma Cell Percentage:**
- **< 5%:** Lower risk.
- **≥5%:** Higher risk.

---

### **Risk Categories:**

#### **1. Low-Risk MGUS:**
- **Criteria:**
- M protein < 1.5 g/dL
- IgG type
- Normal free light chain (FLC) ratio
- **Risk of Progression:**
- **1% per year** (10-15% over 10 years).
- **Monitoring:**
- Blood tests (M protein, FLC) every **6-12 months**.
- Imaging **only if symptoms develop**.

---

#### **2. Intermediate-Risk MGUS:**
- **Criteria:**
- Any **one** of the following:
- M protein ≥1.5 g/dL
- IgA or IgM type
- Abnormal FLC ratio
- **Risk of Progression:**
- **1.5% per year** (15-20% over 10 years).
- **Monitoring:**
- Blood tests every **6 months**.
- Consider imaging (WBLDCT or MRI) **every 1-2 years**.

---

#### **3. High-Risk MGUS:**
- **Criteria:**
- **Two or more** of the following:
- M protein ≥1.5 g/dL
- IgA or IgM type
- Abnormal FLC ratio
- **Risk of Progression:**
- **2-3% per year** (25-30% over 10 years).
- **Monitoring:**
- Blood tests every **3-6 months**.
- Imaging (WBLDCT or MRI) **annually** or sooner if symptoms arise.

---

### **Risk of Progression to Myeloma:**
- **Overall MGUS:** Lifetime risk is approximately **1% per year**.
- **High-risk patients:** Require more frequent monitoring to detect early transformation to **smoldering multiple myeloma (SMM)** or **active myeloma**.

---

### **Next Steps:**
Would you like to discuss your specific risk factors or monitoring plan based on your recent test results?

REPLY
@dcuste

### **Risk Stratification in MGUS: Low, Intermediate, and High Risk**

MGUS (Monoclonal Gammopathy of Undetermined Significance) is stratified into risk categories to estimate the likelihood of progression to **multiple myeloma (MM)** or related disorders. The risk assessment considers clinical and laboratory factors.

---

### **Key Factors for Risk Stratification:**
1. **M Protein Level (Monoclonal Protein)**
- **Low Risk:** < 1.5 g/dL
- **Intermediate/High Risk:** ≥1.5 g/dL

2. **Type of M Protein:**
- **IgG:** Lower risk compared to IgA or IgM.
- **IgA or IgM:** Higher risk.

3. **Free Light Chain (FLC) Ratio:**
- **Normal Ratio:** 0.26 – 1.65
- **Abnormal Ratio:** Outside this range indicates higher risk.

4. **Bone Marrow Plasma Cell Percentage:**
- **< 5%:** Lower risk.
- **≥5%:** Higher risk.

---

### **Risk Categories:**

#### **1. Low-Risk MGUS:**
- **Criteria:**
- M protein < 1.5 g/dL
- IgG type
- Normal free light chain (FLC) ratio
- **Risk of Progression:**
- **1% per year** (10-15% over 10 years).
- **Monitoring:**
- Blood tests (M protein, FLC) every **6-12 months**.
- Imaging **only if symptoms develop**.

---

#### **2. Intermediate-Risk MGUS:**
- **Criteria:**
- Any **one** of the following:
- M protein ≥1.5 g/dL
- IgA or IgM type
- Abnormal FLC ratio
- **Risk of Progression:**
- **1.5% per year** (15-20% over 10 years).
- **Monitoring:**
- Blood tests every **6 months**.
- Consider imaging (WBLDCT or MRI) **every 1-2 years**.

---

#### **3. High-Risk MGUS:**
- **Criteria:**
- **Two or more** of the following:
- M protein ≥1.5 g/dL
- IgA or IgM type
- Abnormal FLC ratio
- **Risk of Progression:**
- **2-3% per year** (25-30% over 10 years).
- **Monitoring:**
- Blood tests every **3-6 months**.
- Imaging (WBLDCT or MRI) **annually** or sooner if symptoms arise.

---

### **Risk of Progression to Myeloma:**
- **Overall MGUS:** Lifetime risk is approximately **1% per year**.
- **High-risk patients:** Require more frequent monitoring to detect early transformation to **smoldering multiple myeloma (SMM)** or **active myeloma**.

---

### **Next Steps:**
Would you like to discuss your specific risk factors or monitoring plan based on your recent test results?

Jump to this post

Let's evaluate your specific risk factors for MGUS progression based on the criteria:

---

### **Your Known Test Results:**

1. **M Protein Levels:**
- **Current:** 1.22 g/dL (November 2024)
- **Trend:** Increasing (from 0.35 g/dL in October 2022)
- **Risk Factor:** Since your M protein is below 1.5 g/dL, this is still in the **low-risk range**, but the upward trend is noteworthy.

2. **Type of M Protein:**
- **Type:** IgM (you mentioned increasing IgM levels)
- **Risk Factor:** IgM MGUS is generally considered **higher risk** than IgG MGUS.

3. **Free Light Chain (FLC) Ratio:**
- **Current Ratio:** 0.8 (down from 1.1)
- **Normal Range:** 0.26 – 1.65
- **Risk Factor:** Your ratio is within the normal range, which is a **low-risk factor**.

4. **Bone Marrow Plasma Cell Percentage:**
- **Status:** Unknown (Have you had a bone marrow biopsy?)
- **Risk Factor:** If < 5%, this would indicate low risk; ≥5% would raise the risk.

---

### **Preliminary Risk Assessment:**

Based on the available information:

- **M Protein Level:** Low-risk threshold but increasing.
- **IgM Type:** Higher risk compared to IgG MGUS.
- **FLC Ratio:** Normal, indicating lower risk.

**Current Assessment:**
You may fall into the **intermediate-risk category**, primarily due to the IgM type and increasing M protein levels. However, additional factors like bone marrow biopsy results and other clinical symptoms are essential for a comprehensive evaluation.

---

### **Recommended Monitoring Plan:**

1. **Blood Tests:**
- **Frequency:** Every **3-6 months**.
- **Tests:**
- **M Protein Level (Serum Protein Electrophoresis - SPEP)**
- **Free Light Chain Assay (FLC)**
- **Complete Blood Count (CBC)** to check for anemia.
- **Creatinine and Calcium Levels** to monitor kidney and bone health.

2. **Imaging:**
- **Baseline Imaging:** If not already done, consider a **WBLDCT** or **MRI** to detect bone lesions.
- **Follow-Up Imaging:** Every **12 months** or sooner if symptoms (like bone pain) develop.

3. **Additional Tests:**
- **Bone Marrow Biopsy:**
- Recommended if M protein continues to rise or new symptoms emerge.
- Helps assess plasma cell percentage.

---

REPLY
@1oldsoul

Thank you for your response. I was born and raised in San Diego but moved to Arkansas in 1994. Sure miss the San Diego weather. Do you feel that NIR has had a positive effect on MGUS? How often and how long (minutes) do you use your machine? Do you use NIR and LLLT together? I have been using both. What type of MGUS do you have-IGM, IGA etc. And when were you first diagnosed?

Jump to this post

Then you might know Escondido, where I lived in the '60s and Fallbrook, where I have lived for the last 15 years.

I have a very low power 850nm and 940nm LEDs that I use randomly on various areas for about 10 minutes per day. I've been doing this for over a year. I was interested in this to boost cell mitochondria and haven't really seen any benefits. I was diagnosed with IGM MGUS in Apr 2023.

REPLY
@dcuste

Reply to @1oldsoul

When I first started this journey, I based my Hematology questions on ashpublications article on How to manage MGUS
Awhile back, I did contact the people running this study...... clinicaltrials study NCT04731844 but was told I couldn't participate without going to NY for testing. They didn't respond to my other questions on their curcumin specifics.

One of the reasons my hematologist/oncologist gave for not recommending the bone biopsy was my κ/λ ratio of 0.8 wasn't that bad. I did mention that I had a recent episode of unexplained back pain, but it had subsided. That is when she recommended the pet scan.
Another concern I have that she seems to ignore is my LDH has always been high. The last test, 18 months ago, was still 193 down from 240 a year earlier, but still high.
I put all my lab results into ChatGPT. Here is it's response....

While there's no guaranteed way to stop the progression of **MGUS** to more serious conditions like **multiple myeloma**, some strategies may help slow the progression or reduce risk factors. Here's an evidence-based approach:

---

### **1. Maintain a Healthy Lifestyle:**
- **Balanced Diet:**
- Focus on an **anti-inflammatory diet** rich in fruits, vegetables, whole grains, lean proteins, and healthy fats (like omega-3s from fish or flaxseed).
- Reduce processed foods, refined sugars, and saturated fats.
- **Stay Hydrated:**
- Adequate hydration supports kidney function, which is important since MGUS can affect the kidneys.
- **Regular Exercise:**
- Engaging in **moderate exercise** (e.g., walking, swimming) for at least **150 minutes per week** can improve overall health and boost the immune system.
- **Strength training** helps maintain bone health, crucial for preventing bone complications common in myeloma.

---

### **2. Manage Underlying Health Conditions:**
- **Control Chronic Diseases:**
- **Diabetes, hypertension, and obesity** may contribute to MGUS progression. Work with your doctor to keep these conditions well-managed.
- **Monitor Kidney Function:**
- Keep an eye on your **creatinine levels** and **GFR** (glomerular filtration rate).

---

### **3. Reduce Inflammation and Oxidative Stress:**
- **Anti-inflammatory Supplements:**
- **Curcumin (Turmeric):** Some studies suggest it may help slow the progression of MGUS due to its anti-inflammatory and antioxidant properties.
- **Vitamin D:** Low levels are common in MGUS patients; ensuring adequate intake may reduce progression risk.
- **Avoid Smoking and Excessive Alcohol:**
- Both can increase oxidative stress and inflammation.

---

### **4. Monitor and Manage Infections:**
- Chronic or recurrent infections can strain the immune system and potentially accelerate progression. **Vaccinations** (like flu and pneumonia vaccines) can help prevent infections.

---

### **5. Stress Management:**
- **Chronic stress** can negatively impact the immune system. Practices like **meditation**, **yoga**, and **deep breathing exercises** can help.

---

### **6. Regular Monitoring and Early Intervention:**
- **Follow-up Testing:**
- Regular monitoring of **M protein levels**, **free light chains**, and **LDH** is crucial.
- **Prompt Attention to Symptoms:**
- Report any new symptoms (fatigue, bone pain, infections) to your doctor immediately.

---

### **Potential Future Therapies:**
There’s ongoing research into preventive treatments for high-risk MGUS patients, such as:
- **Immunomodulatory drugs (IMiDs):** May one day be used preventively, but currently, no treatment is standard for MGUS without progression signs.

---

### **Key Takeaway:**
While you can't completely prevent progression, adopting a healthy lifestyle, managing chronic conditions, and staying vigilant about your health can help slow the process. Discuss these strategies with your healthcare provider to tailor an approach that suits your specific situation.

I'm in San Diego and am with Kaiser Senior Advantage HMO plan. I haven't been to any specialty clinics. She did indicate she has quite a bit of MGUS experience and didn't recommend that I get a second opinion. I could tell her frustration with big pharma not devoting resources to work on treatments that don't have enough of a return on investment. I do subscribe to IWMF . They seem to have very high hopes on finding a cure soon.
I have been using NIR as an overall cell treatment for about a year now.

Jump to this post

Could you tell me what LFH
NIR. And IMIDS are. Thank you so much for all the information you provided. I am so scared of progression to full blown MM.

REPLY
@circawdm

Good morning, I have had the diagnosis for four years. I am a 75-year-old caucasian male. I have the Lamda variety of monoclonal antibodies, so I do have some peripheral neuropathy in my feet. My initial M-Spike was only .8. Free light chains and ratio were not too bad.

With no other symptoms or medical issues that could complicate things, and being in the low-risk category, my hematologist/oncologist put me in a wait-and-watch category, and I have blood labs every 4 months. He said I could go every 6 months, but I feel more comfortable with 4 months because my monocytes are a bit high.

I have studied medicine for 50 years as a serious hobby, and for the past 30 years, I have looked upon my health and treatments with a homeopathic or holistic approach, unless I needed an antibiotic or something was too severe for me to handle myself. So I read up on everything about MGUS. I saw common threads from those who had doctors or other medical advisors, looked at studies, etc.

I decided to go on a "Mediterranean Diet" immediately. No sugar, no processed foods, no fried foods, etc. No red meat. It was easy for me because I had been eating pretty healthy for years. My weight was very good. I also cut out other things that cause inflammation in the body and irritate the nerves (the peripheral neuropathy was pretty painful at first). So, I cut out caffeine and any added salt. I started doing exercises for my legs and feet to improve my circulation, I exercised daily as best I could, and meditated to keep my stress levels low.

Importantly, I researched the best most tested supplements for lowering inflammation, killing cancerous cells, and building the immune system. I take D3, **turmeric/curcumin, **Omega 3 Fish Oil gel caps, C, E, Alpha Lipoic Acid, PEA, garlic (natural form and gel pills), a good multi-vitamin-mineral pill, low dose iron, and 2-3 other things that are very powerful antioxidants. I get them on Amazon, so the monthly price is not bad.

While research is still ongoing, current evidence from many studies suggests that high sugar intake, particularly from added sugars in drinks like soda, can potentially increase the risk of developing MGUS (Monoclonal Gammopathy of Undetermined Significance) and other cancers by contributing to obesity, promoting inflammation, and potentially impacting insulin levels, which can fuel cancer cell growth. A balanced diet is crucial for overall health, including for those with MGUS or other cancers.

My peripheral neuropathy and my MGUS blood tests began to improve after 4 months. In the last four years, my peripheral neuropathy symptoms are 60-70% better, and my MGUS tests have consistently gotten lower or stayed stable. My recent tests showed only a .3 M-Spike and normal Free Light Chains ratio and my other bloodwork related to MGUS was either stable or lower.

I found for me, and others I have read about in several well-known studies, that MGUS has to be treated with a multi-disciplinary approach. Unless it is at the point where medical intervention is needed, diet, exercise, supplements, low stress, and daily exercise seem to help slow or even reverse progression. This has been studied with tens if not hundreds of thousands of people now for many years.

So that is my experience. My oncologist calls me "boring," and said if his patients with MGUS and other more serious cancers in their early stages in particular, would follow a diet and other things I am doing, they would be so much better off. It's simply healthy for everyone to ditch processed sugar and foods, fried/fast food, etc. But too many people simply want their sugar and their fast food, etc. They won't do what is needed to lose weight.
And that is certainly their choice. I decided I was not going to allow the MGUS to progress if I could avoid it. So far, all I have been doing has worked. I don't miss sugary food, fast food, red meat or any other of the highly inflammatory. foods. It's like when I quit smoking 40 years ago. After I quit I did not miss it at all and the smell of smoke bothered me.

So that's my story. Everyone is different, but one thing that cannot be denied and which is a proven fact is that inflammation is behind disease processes, and the less inflammation our bodies have in our cells and tissues and organs, the more likely we are to be healthy or healthier.

Jump to this post

Good morning. I would like to ask you a couple of questions about your diet and supplements. What percentage on average is meat to plant based per day and do you limit meat to once per day? I have seen many variations of the Mediterranean diet. What about grass fed pork, wild venison and eggs? I could go completely vegan today but my digestive system does not handle beans and legumes well so I am going to have to transition slowly to make sure I get enough complete protein in my diet. Also can you tell us how much turmeric/curcumin you take per day? Lots of clinical trials on its efficacy for slowing progression of MGUS but I don’t remember reading about the dosages. Turmeric does wonders for me for back pain- less so with curcumin. My back pain predates MGUS- caused by scoliosis and now some degenerative disc disease. A combination of turmeric, curcumin and walking every day almost completely keeps my pain at bay unless I do too much heavy lifting or bending over with yardwork like raking, weedeating etc. And finally, do you take the R or S-Lipoic acid? I have read many reports that R is better assimilated and recently found out by contacting Doctors Best (the brand I have been taking) that it is 50/50 R and S although they told me they do make one with just R-Lipoic. With that being said, even with 50/50 it gives me a ton of energy. Thanks for taking the time to share your expertise because your results speak for themselves and I know there are so many on this forum who are desperate to do something other than watch and wait.

REPLY
@dcuste

Then you might know Escondido, where I lived in the '60s and Fallbrook, where I have lived for the last 15 years.

I have a very low power 850nm and 940nm LEDs that I use randomly on various areas for about 10 minutes per day. I've been doing this for over a year. I was interested in this to boost cell mitochondria and haven't really seen any benefits. I was diagnosed with IGM MGUS in Apr 2023.

Jump to this post

We were neighbors then! I lived in San Marcos and lastly, Fallbrook before I moved to Arkansas. I worked at the Fallbrook hospital in purchasing. My machine is also low level 660 nm and 850 nm but based off my results with plantar fasciitis, I know it has to help other areas. Hope you read the post by @circawdm. He’s had some impressive results and it has really given me hope!

REPLY

Thank you for this! ChatGPT is awesome. The info is horrifying to say the least even though doctors tell you “no worries”. I am going to insist on WBLDCT if my hematologist insists the scans are necessary after my BMB (bone marrow biopsy) Thank you so much for your time and thoughtfulness. God bless you and my prayers are with you through your journey. I look forward to one of us sharing some positive feedback in the near future!

REPLY
@amyboylan1

Could you tell me what LFH
NIR. And IMIDS are. Thank you so much for all the information you provided. I am so scared of progression to full blown MM.

Jump to this post

Don't assume I have any medical knowledge about MGUS or anything else. I don't even fully trust AI to fully get it right. But here is how ChatGPT responded to your question.......
### **1. LFH (Likely Typo)**
There isn't a standard medical acronym **LFH** related to MGUS or oncology. Did you mean **LDH** (Lactate Dehydrogenase)?
If **LFH** stands for something specific, please clarify, and I'll help further.

---

### **2. NIR (Near-Infrared Spectroscopy)**
**NIR** typically refers to **Near-Infrared Spectroscopy**, a non-invasive imaging technology that uses near-infrared light to analyze tissues.
- **Medical Use:** Primarily in brain monitoring, muscle oxygenation, and some cancer diagnostics.
- **Not directly related** to MGUS but may be used in advanced research or diagnostic imaging.

---

### **3. IMiDs (Immunomodulatory Drugs)**
**IMiDs** are a class of drugs that **modulate the immune system** and are used in treating conditions like **multiple myeloma**. They work by:
- **Inhibiting tumor growth**
- **Enhancing the immune response** against abnormal cells
- **Suppressing inflammatory cytokines**

**Common IMiDs include:**
1. **Thalidomide** (first-generation IMiD)
2. **Lenalidomide** (Revlimid)
3. **Pomalidomide** (Pomalyst)

**Use in MGUS:**
- **Not typically used for MGUS** because treatment is usually not needed unless progression occurs.
- IMiDs are prescribed for **smoldering multiple myeloma** or **active multiple myeloma**.

---

### **Clarification Needed:**
If **LFH** or **NIR** had different meanings in your context, feel free to share more, and I'll adjust the explanation!

REPLY
@1oldsoul

@loribmt
@gingerw
Lori and Ginger, I am hoping you have some insights after reading your very helpful thread on Second Opinions. Any thoughts on how I can find out what the standards are (IGM numbers) when it comes to when bone biopsies and full body scans become necessary? I would like to see if I can get a second opinion but is it going to offend my Hematologist?

Jump to this post

Here are some links regarding further testing. I had
a baseline bone marrow biopsy (BMB) 8 years ago when first diagnosed (I wanted to know my starting point). Normal marrow has around 2-3% plasma cells and that showed 5%. I had a BMB this summer because my kappa is now 300 and my kappa/lambda is 29. It showed +15% plasma cells, which should be in the SMM range but my oncologist said still MGUS due to other test results. The genetic test showed 1q21 gain, a genetic mutation that ~40% of MM patients have and that impacts treatment (good [?] to know upfront even if I don't get MM). I like knowing my status, even if the news isn't all that good. I have IgA kappa MGUS.
https://pmc.ncbi.nlm.nih.gov/articles/PMC7203099/ https://pmc.ncbi.nlm.nih.gov/articles/PMC3319353/https://pmc.ncbi.nlm.nih.gov/articles/PMC9425303/

REPLY
@circawdm

Good morning, I have had the diagnosis for four years. I am a 75-year-old caucasian male. I have the Lamda variety of monoclonal antibodies, so I do have some peripheral neuropathy in my feet. My initial M-Spike was only .8. Free light chains and ratio were not too bad.

With no other symptoms or medical issues that could complicate things, and being in the low-risk category, my hematologist/oncologist put me in a wait-and-watch category, and I have blood labs every 4 months. He said I could go every 6 months, but I feel more comfortable with 4 months because my monocytes are a bit high.

I have studied medicine for 50 years as a serious hobby, and for the past 30 years, I have looked upon my health and treatments with a homeopathic or holistic approach, unless I needed an antibiotic or something was too severe for me to handle myself. So I read up on everything about MGUS. I saw common threads from those who had doctors or other medical advisors, looked at studies, etc.

I decided to go on a "Mediterranean Diet" immediately. No sugar, no processed foods, no fried foods, etc. No red meat. It was easy for me because I had been eating pretty healthy for years. My weight was very good. I also cut out other things that cause inflammation in the body and irritate the nerves (the peripheral neuropathy was pretty painful at first). So, I cut out caffeine and any added salt. I started doing exercises for my legs and feet to improve my circulation, I exercised daily as best I could, and meditated to keep my stress levels low.

Importantly, I researched the best most tested supplements for lowering inflammation, killing cancerous cells, and building the immune system. I take D3, **turmeric/curcumin, **Omega 3 Fish Oil gel caps, C, E, Alpha Lipoic Acid, PEA, garlic (natural form and gel pills), a good multi-vitamin-mineral pill, low dose iron, and 2-3 other things that are very powerful antioxidants. I get them on Amazon, so the monthly price is not bad.

While research is still ongoing, current evidence from many studies suggests that high sugar intake, particularly from added sugars in drinks like soda, can potentially increase the risk of developing MGUS (Monoclonal Gammopathy of Undetermined Significance) and other cancers by contributing to obesity, promoting inflammation, and potentially impacting insulin levels, which can fuel cancer cell growth. A balanced diet is crucial for overall health, including for those with MGUS or other cancers.

My peripheral neuropathy and my MGUS blood tests began to improve after 4 months. In the last four years, my peripheral neuropathy symptoms are 60-70% better, and my MGUS tests have consistently gotten lower or stayed stable. My recent tests showed only a .3 M-Spike and normal Free Light Chains ratio and my other bloodwork related to MGUS was either stable or lower.

I found for me, and others I have read about in several well-known studies, that MGUS has to be treated with a multi-disciplinary approach. Unless it is at the point where medical intervention is needed, diet, exercise, supplements, low stress, and daily exercise seem to help slow or even reverse progression. This has been studied with tens if not hundreds of thousands of people now for many years.

So that is my experience. My oncologist calls me "boring," and said if his patients with MGUS and other more serious cancers in their early stages in particular, would follow a diet and other things I am doing, they would be so much better off. It's simply healthy for everyone to ditch processed sugar and foods, fried/fast food, etc. But too many people simply want their sugar and their fast food, etc. They won't do what is needed to lose weight.
And that is certainly their choice. I decided I was not going to allow the MGUS to progress if I could avoid it. So far, all I have been doing has worked. I don't miss sugary food, fast food, red meat or any other of the highly inflammatory. foods. It's like when I quit smoking 40 years ago. After I quit I did not miss it at all and the smell of smoke bothered me.

So that's my story. Everyone is different, but one thing that cannot be denied and which is a proven fact is that inflammation is behind disease processes, and the less inflammation our bodies have in our cells and tissues and organs, the more likely we are to be healthy or healthier.

Jump to this post

I like your overall plan and think I'll adopt it. I already take many of the same supplements as you and today started adding the Turmeric/Curcumin C3. Had to stop taking the Pradaxa. Also ordered the Alpha Lipoic Acid, and PEA. Should arrive tomorrow.
I've been fermenting garlic in honey and taking a clove or two each morning for about a year now.
Been using a Stelo CGM about a month. They are available without a prescription. It helps with managing blood sugar levels. My A1c is lower now than it has been in years. I'm going on the theory that a lower sugar will help.

REPLY
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