Showing posts with label berkson. Show all posts
Showing posts with label berkson. Show all posts

Saturday, June 5, 2010

Treating Hepatitis C with Low Dose Naltrexone (LDN)

3 mg. LDN next to Advil



UPDATE 2013 LDN DOSING - WHY 3 MG LDN MIGHT BE BEST -


Treating Hepatitis C with Low Dose Naltrexone (LDN)

UPDATE - JUNE 2014 -

The original post below was written back in 2010 but I have since edited it to reflect the newer research regarding using the lowest dose possible of LDN.

Please also see:   Why 3 mg Low Dose Naltrexone Might Be Best


After being on 3mg Low Dose Naltrexone for 5 years now, my HCV viral load still remains low and my liver enzymes are still normal.  And even though I imagine that in the next year or so, I will do the newest non-interferon treatment - minus the ribavirin, I still plan on taking Low Dose Naltrexone for the rest of my life - virus or no virus.  Meanwhile, now that a possible real cure for HCV has come along, most folks cannot afford it at this time.  So the best bet is to take Low Dose Naltrexone, use good quality supplements that help support one's liver and immune system and to eat as healthily as possible.  A paleo type diet and one that does not involve grains or any kind, particularly wheat.



I am successfully managing my Hepatitis C virus by using LDN - Low Dose Naltrexone, supplements, diet and exercise and have attempted to share my experiences on my blog, Nola Hepper. Now, I have tried to include all of this information in one place.

I was diagnosed in 2002 with Hepatitis C, genotype 1b. A biopsy revealed minor inflammation with Grade 0-1, Stage 0-1 and my lab work showed slightly elevated liver enzymes. Despite being urged to due interferon/ribavirin treatment back then, I chose to make healthy life style changes instead while waiting for "something else" to come along and learned as much as I could about the HCV virus. My health remained about the same for several years until 2005, when my Hurricane Katrina experience caused me to start having severe side effects. I developed fibromyalgia, shingles, severe chemical sensitivities and terrible IBD. My doctors told me that all of these problems were being caused by the Hep C and again urged me to do treatment.

I was able to get Social Security disability and Medicare and this allowed me to see a very good integrative doctor. She tested me for everything and suggested a course of action for me, which included several new supplements and diet changes. She also gave me a paper written by Dr. Burt Berkson, another integrative doctor who had done extensive work using ALA - Alpha-Lipoic-Acid. His work seemed very promising, so I began to do his protocol of ALA, Milk Thistle (although I had already been taking milk thistle for years), Selenium, and B Complex along with the other supplements that my doctor had recommended for me.

One of the diet changes that my doctor mentioned was to cut down or eliminate wheat - she said that most people cannot really digest it or are sensitive to it. I was a bit skeptical but after researching it, I decided to try it out. And the results were amazing! Within days it seemed that my IBD and bloating had greatly improved. Soon, I noticed that my fibromyalgia had gotten much better as had my chemical sensitivities - I didn't' seem to be quite so sensitive to smells anymore - and you must understand. It had been to the point where going to the grocery was an ordeal - I had to hold my breath going down the detergent or bug spray aisles. This also was much improved! Gluten (one of the proteins found in wheat) is a big problem to most folks with liver disease, particularly those who undergo interferon treatment, as it is a known trigger for celiac disease and can cause elevated liver enzymes.

After researching more about diet and nutrition, which included an appointment with a Certified Clinical Nutritionist, I took things a step further and ordered a food sensitivity/intolerance panel through a company called Alletess as they took my Medicare insurance. This test revealed that I had sensitivities to cow's milk, yeast and some shellfish. Upon eliminating these foods, my IBD really seemed to completely go away and my other health issues got much better as well.

However, my latest liver lab work (January 2009) was frustrating - my HCV viral load test was 1,400,000 - ALT was 174 and AST at 105 - other labs were pretty much in the normal range with a few blips here and there. I had exchange emails with a couple of folks who had seen Dr. Berkson and they said that they liked him and were seeing great improvements in their health - they also mentioned that he had put them both on Low Dose Naltrexone or LDN. So I decided to go out to New Mexico to see him myself.

I started on 3 mg. of LDN in mid-February 2009 while at Dr. Berkson's clinic but after I got back, I started having an upset stomach due to the lactose filler that the pharmacy in New Mexico used in their compounding mixture. I went off of the LDN for about 2 weeks until I got a new prescription mixed with acidophilus - probably March 1st, 2009. I had new labs done in late April 2009 and the results were remarkable. Viral load dropped from the 1,400,000 to 48,000! ALT from 174 to 22 and AST from 105 to 30!. My integrative doctor was amazed as I was but my traditional gastro actually yelled at me, saying that LDN was not "supposed" to treat Hepatitis C and that the labs had to be a mistake. I've never gone back to him.

This is about the time that I became an advocate for LDN and started posting more on my blog and on several LDN yahoo groups and various Hepatitis C, health sites, etc. How could I not with the results that I have had? Since that time, I have played around with the LDN dosage and have used my lab results as a kind of rough guide in doing so. Currently I am back on 3 mg. that I take most every night. My May 2010 lab work showed a viral load of 11,400 - ALT at 25; AST at 30.  (note - 2014 LDN dosage is 3mg taken every other night or every third night)

Ideally, it is best to work with a doctor who is familiar with the workings of LDN and who can prescribe it. And to get the LDN from a reputable compounding pharmacy such as Skip's Pharmacy. However, one can also order the 50 mg. tablets and make the solution themselves without a prescription.

If you already have a prescription for LDN, it is probably in a capsule form. If you want to start off at a different dose than whatever your prescription is for, it is better to mix the LDN with water than to simply take a third or half of the capsule alone. The reason being is that one can never be sure where the LDN is in the capsule and if you mix it with water, it is a more accurate dose. For example, I take my 3 mg. capsule and dump it into a dark colored vial (I got a 12 ml (cc) vial at Whole Foods for a couple of bucks). Use a 1 cc (ml) or 3 cc (mg.) syringe and measure in 3 ml. of distilled or bottled water - not tap water. Measure out the needed dose and store the rest in the fridge. For 4.5, simply increase to 4.5 cc's (ml's) of water.


There are slightly different instructions for the 50 mg. tablet but it is the same principal - 50 cc's (ml's) of water mixed with the tablet - obviously you would need a vial large enough for that amount - more detailed instructions are included in one of the links above or here: "How to Obtain Low Dose Naltrexone"

"Once you have a supply of 50 mg Naltrexone tablets, you can convert them as needed to LDN. To do so, fill a graduated cylinder with 50 ml of distilled water (unlike tap or spring water, distilled water contains no impurities that could potentially react with and thus reduce Naltrexone's effectiveness). Pour the water from the graduate into a 4 oz amber glass jar with a tight-fitting lid. Then add a 50 mg Naltrexone tablet. The tablet will mostly dissolve in about five to ten minutes. Since not all of the tablet is soluble in water, instead of yielding a clear solution, the result will be a cloudy suspension. It must be shaken each time before use to evenly disperse all the undissolved particles. One ml of the (shaken) suspension will contain one mg of Naltrexone. Use a graduated baby medicine dropper to measure out the dose you need."


Dosing is very individualized. I am finding that the biggest mistake that doctors are making with LDN is to prescribe the 4.5 dosage in the beginning, particularly to their patients with liver disease - some folks can tolerate this dosage, but in most it is a guarantee of initial side effects - sleep disorders being the most frequent. There are different theories on dosing, depending on what doctor or researcher you listen to. Dr. Berkson starts everyone off at 3 mg. but he prescribes sleep medications in the first month to counteract these sleep problems. Most savvy doctors and LDN veterans know to recommend that people start off at a very low dose such as 1 mg. Start at 1 mg. and stay on it for a week or so then move up to 1.5 or 2 for another week or so until you get to 3 mg. At this point, you can either work your way up to 4.5 or stay at the 3 mg. dosage until you get your first post LDN labs done. Again, dosing is very individual - up to that person's make up, medical problems, etc.  - some folks do well on 3 mg and have great results while others need more or less of the Low Dose Naltrexone - some folks take it every other night or less.  It really depends greatly on what disorder or multiple disorders the person has along with other factors.


Why LDN might not work -  According to several sites and personal accounts, yeast infections seem to be triggered or made worse when first starting LDN.  It is very important to have any candida, or other mold/yeast problems cleared up as having them can interfere with how well the LDN works.

The link below covers this as well as other side effects - note - the site was written by someone with MS, but it is still good info:


Side Effects & Dosing of Low Dose Naltrexone (LDN)


Dr. McCandless ( Children with Starving Brains )  has written about the dietary aspect when using LDN:


Dr McCandless, seldom is LDN stand-alone treatment



There is much more LDN info on other sites:

LDNers.org site - Resouces page


I have covered supplements in another area of the blog -  Supplements 

a quick recap.  The most important supplements for the liver are those that help generate more glutathione,  - usually ALA - alpha-lipoic-acid, with  NAC - N-acetyl cysteine, SAMe, whey protein (gluten-free) and others.

Silymarin (Milk Thistle) is extremely important as is Vitamin D3.  Most folks are very deficient in Vitamin D3, particularly in those with HCV.   A multi vitamin without iron! (capsule form is best and more easily absorbed than tablet), vitamins C & E.

One of the most critical things is to keep one's ferritin levels below 100.  Ferritin is basically the iron storage in the liver - and it is the iron that does all of the damage!!!  Not the HCV virus as most docs and literature would have one believe.  See Iron Ferritin and the Liver for more.

Tuesday, November 10, 2009

Dr. Berkson's 2009 Videos - Pancreatic Cancer, RA, Lupus, Lymphoma, more

Dr. Berkson was the keynote speaker at the recent Low Dose Naltrexone Conference held in Bethesda Md. at the NIH - National Institute of Health. There, he presented a 2 hour presentation detailing his successful treatments of various disorders, including pancreatic cancer, b-cell lymphoma, RA, Lupus, breast cancer, liver cancer and cirrhosis, among other diseases.

Newly published abstract about Dr. Berkon's use of ALA and LDN in treating 3 pancreatic cancer patients:


Revisiting the ALA/N (alpha-lipoic acid/low-dose naltrexone) protocol for people with metastatic and nonmetastatic pancreatic cancer: a report of 3 new cases.


Berkson BM, Rubin DM, Berkson AJ.




The Integrative Medical Center of New Mexico, Las Cruces, NM, USA.

The authors, in a previous article, described the long-term survival of a man with pancreatic cancer and metastases to the liver, treated with intravenous alpha-lipoic acid and oral low-dose naltrexone (ALA/N) without any adverse effects. He is alive and well 78 months after initial presentation. Three additional pancreatic cancer case studies are presented in this article. At the time of this writing, the first patient, GB, is alive and well 39 months after presenting with adenocarcinoma of the pancreas with metastases to the liver. The second patient, JK, who presented to the clinic with the same diagnosis was treated with the ALA/N protocol and after 5 months of therapy, PET scan demonstrated no evidence of disease. The third patient, RC, in addition to his pancreatic cancer with liver and retroperitoneal metastases, has a history of B-cell lymphoma and prostate adenocarcinoma. After 4 months of the ALA/N protocol his PET scan demonstrated no signs of cancer. In this article, the authors discuss the poly activity of ALA: as an agent that reduces oxidative stress, its ability to stabilize NF(k)B, its ability to stimulate pro-oxidant apoptosic activity, and its discriminative ability to discourage the proliferation of malignant cells. In addition, the ability of lowdose naltrexone to modulate an endogenous immune response is discussed. This is the second article published on the ALA/N protocol and the authors believe the protocol warrants clinical trial.

PMID: 20042414 [PubMed - in process]


UPDATE - May 2013 - OGF info in Pancreatic Cancer -
Newer info show that LDN itself might not be effective with PC as reported -

An explanation from Jayne Crocker -

For pancreatic cancer it is a methylation problem. I know there are some physicians who believe one way of getting around this is to give LDN to patients at night (to build up the OGF receptors) and then inject them with OGF in the day. Whether this is any more effective for pancreatic cancer than just taking OGF directly remains to be seen.


Everyone who has a chronic disease has HPA axis issues, so we are all likely to have reduced receptors. The HPA axis is skewed by the chronic sickness syndrome, which results in a weakened immune response (<10 a="" advanced="" ago="" all="" also="" amp="" and="" but="" cancer="" carcinoma="" cell="" characteristic="" chronic="" defect="" degrades="" discovered="" dr="" endorphin="" f="" has="" head="" i="" important="" in="" is="" it="" know="" loss="" mclaughlin="" nbsp="" neck="" normal="" not="" number="" of="" ogf="" posted="" rather="" receptor.="" receptor="" receptors="" remember="" s="" sickness="" specifically="" squamous="" stages="" study="" that="" the="" too="" we="" while="" work="" you="">
This is why LDN is so important in the sense that it builds up the receptors which is what increases the production of endorphins really. There are many cells in the body that produce endorphins, even T cells produce endorphins heavily during an inflammation. So if LDN drives up the OGF receptors, then it reverses one of the HPA axis problems when skewed. Adrenal Fatigue is one possible symptom when the HPA axis gets skewed.

If you are in a position to consider taking OGF directly (rather than count on LDN’s rebound effect to gain from this), I would strongly recommend trying this. Unfortunately it costs about $1,000/month so I’m not sure if this is a possibility.


OGF is Opioid Growth Factor which is the good endorphin that we all count on to benefit from taking LDN. However if there is no OGF receptor present, LDN will not be an effective treatment. If you bypass LDN, and go straight to taking OGF, this may help.

The reason LDN struggles with being effective for those with pancreatic cancer, is because the pancreas when diagnosed with cancer is unable to metabolize LDN. The problem is, when the body tries to make OGF in the pancreas, it can’t. When taking OGF directly, this works because your body doesn’t need to make it, ie metabolize it, it’s already a finished product. This effect is not possible by just taking LDN. So by taking OGF you are bypassing the problem. Please see the below email from Dr Zagon:

About 20 years ago we did an experiment with LDN and OGF as to pancreatic cancer. Amazingly to us, LDN had no effect and OGF was terrific. This was the first time we had ever seen that LDN did not work.

Well, it turns out later that while investigating pancreatic cancer, a number of researchers (not us) found that the body has a methylation of OGF precursors - called preproenkephalin. Methylation of preproenkephalin does not allow the full division of the larger preproenkephalin molecule into smaller peptides such as met-enkephalin (OGF). The bottom line is that pancreatic cancer cells do not have access to making OGF. So, if LDN works by increasing OGF (and its receptor OGFr) which can come together when LDN is no longer present - and this would normally have a super reaction by inhibiting cell proliferation, then in pancreatic cancer LDN is not going to work. It cannot upregulate - increase- OGF. As OGF is not present.

Should you wish to learn more about OGF, check out the LDNScience website http://www.ldnscience.org/opioid-growth-factor-ogf/how-does-ogf-work

But note the word methylation - perhaps Dr. Berkson's success with PC was due to the use of IV Lipoic Acid, along with other supplements - his protocol does increase methylation.

PubMed abstract on OGF and PC:

Opioid growth factor improves clinical benefit and survival in patients with advanced pancreatic cancer.



Smith JP, Bingaman SI, Mauger DT, Harvey HH, Demers LM, Zagon IS.

Department of Medicine, Pennsylvania State University, College of Medicine, Hershey Medical Center, Hershey, PA, USA.

BACKGROUND:

Advanced pancreatic cancer carries the poorest prognosis of all gastrointestinal malignancies. Once the tumor has spread beyond the margins of the pancreas, chemotherapy is the major treatment modality offered to patients; however, chemotherapy does not significantly improve survival.

OBJECTIVE:

Opioid growth factor (OGF; [Met(5)]-enkephalin) is a natural peptide that has been shown to inhibit growth of pancreatic cancer in cell culture and in nude mice. The purpose of this study was to evaluate the effects of OGF biotherapy on subjects with advanced pancreatic cancer who failed chemotherapy.

METHODS:

In a prospective phase II open-labeled clinical trial, 24 subjects who failed standard chemotherapy for advanced pancreatic cancer were treated weekly with OGF 250 µg/kg intravenously. Outcomes measured included clinical benefit, tumor response by radiographic imaging, quality of life, and survival.

RESULTS:

Clinical benefit response was experienced by 53% of OGF-treated patients compared to historical controls of 23.8% and 4.8% for gemcitabine and 5-fluorouracil (5-FU), respectively. Of the subjects surviving more than eight weeks, 62% showed either a decrease or stabilization in tumor size by computed tomography. The median survival time for OGF-treated patients was three times that of untreated patients (65.5 versus 21 days, p < 0.001). No adverse effects on hematologic or chemistry parameters were noted, and quality of life surveys suggested improvement with OGF.

LIMITATIONS:

Measurements other than survival were not allowed in control patients, and clinical benefit comparisons were made to historical controls.

CONCLUSION:

OGF biotherapy improves the clinical benefit and prolongs survival in patients with pancreatic cancer by stabilizing disease or slowing progression. The effects of OGF did not adversely alter patient quality of life. The use of OGF biotherapy at earlier stages of disease or in combination with other chemotherapeutic agents may further improve the outcome of this malignancy.

PMCID: PMC2947031 Free PMC Article

PMID: 20890374 [PubMed]

 

Even though I have provided these links in an older post, "Dr. Berkson & LDN" , these videos have just been made available and contain crucial information that might save countless numbers of people. His successful treatment of a patient with pancreatic cancer will be published in December, along with 2 other cases.
Introductory remarks - ALA - Hepatitis C

1) http://www.youtube.com/watch?v=WHyUfHqR4PA


Pet Scans - Treatment Protocol - ALA Explanation - Pancreatic Cancer with Mets to Liver (case to be published in December)

2) http://www.youtube.com/watch?v=xy65UGsVMac

Pancreatic Cancer with Mets to Liver - Hepatitis C with Liver Cancer -

3) http://www.youtube.com/watch?v=dRf8Xuqhb5Q

RA with Lymphoma from Humira - B Cell Lymphoma - Breast Cancer - Rheumatoid Disorders - Dermatomyositis -

4) http://www.youtube.com/watch?v=RXz3VIuyHHk

RA - SLE (Lupus) -

5) http://www.youtube.com/watch?v=nttilGKpJvU


ALA and purity; Asian products vs European - ALA discussion - Epstein-Barr Virus -

6) Dr Berkson Q & A Part One

http://www.youtube.com/watch?v=RsBN78Cl1s4
Lab Tests - Dosing of LDN and ALA - R Form Lipoic Acid - B Complex -

7) Dr Berkson Q & A Part Two:


http://www.youtube.com/watch?v=c29DAE4MGmo

Pancreatic Cancer & Thoughts on Treatment - ALA Gene Expression - Misc.

8) Dr. Berkson Q & A Part Three:

http://www.youtube.com/watch?v=nYxzDuKAdfI

http://www.drberkson.com/