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Tuesday, November 6, 2018

Phlebotomy or Venipuncture And Multiple Sclerosis



We need to jump ahead into the present day, being October 2018.
I am treading on new ground, that my Endocrinologist, Neurologist GP, and Cancer Dr have not seen

the ancient art of blood letting,  or now called a Phlebotomy is used in only one disease.
I have primary progressive multiple sclerosis.  This is the USA term, phlebotomy.  Not was expecting another diagnosis, or was I looking for one.

This is being updated Aug 2020 for my UK audiences correction. 
Phlebotomy is the collection of blood by one of several methods. These methods include: 1) performing a finger puncture with a small lancet to let blood drain from capillaries, which is then collected into a very fine glass tube (capillary tube), a pediatric (microtainer) collection tube, or onto blotter paper; 2) a heel puncture, in lieu of a finger puncture, for neonates and infants; 3) venipuncture; and 4) arteriopuncture or arterial puncture.

Venipuncture, as it relates to phlebotomy, is using a needle to puncture a vein from which to collect blood into a syringe or evacuated tube. (Venipuncture can also be used to introduce into a vein a fluid, such as a medication or a contrast for radiology, but that falls outside the scope of phlebotomy.)


I have been on testosterone therapy for years now. A Endocrinologist was watching over me for also needing 150,000 iu a week of vitamin D to keep my numbers up.  She had taken me off testosterone, to do a MRI of the pituitary gland, to ensure no tumor. Nothing was found. It was difficult on the mind to cold stop testosterone, for anybody thinking of stopping.

My blood, I've always been told it's thick, or large cells. I could not get my testosterone level up. My hematocrit and hemoglobin has always ran high for years. My heart Dr said, while sitting, it's like MS always has me running a marathon.

Many EKG done by other doctors, because of excessive pulse and numbers.  but what I was not expecting was for the endocrinologist to send me to the cancer unit.

My Newest Dr was one at ease, saying it was the testosterone therapy causing thick blood. I told him endocrinologist said it was not. He agreed to run some tests. A DNA of the Jak2 gene, and others,

The JAK2 gene mutation test identifies whether there is a mutation on the JAK2 gene that could cause a myeloproliferative disorder. Polycythemia vera is one of the diseases with a high correlation with a JAK2 mutation.
Mine was negative, but my Iron was off the chart.

He then ran the HFE gene.  I have a great GP that also mentioned This gene. This consist of the C282Y and h63d gene.  I was given one gene from each parent, along with brothers and sisters, and going backwards thru family tree on both sides, to aunts, uncles, cousins, ect.

Hereditary hemochromatosis is present at birth. But, most people don't experience signs and symptoms until later in life — usually between the ages of 40 and 60 in men and after age 60 in women. Women are more likely to develop symptoms after menopause, when they no longer lose iron. My Neurologist niece was diagnosed at the age of 17.

But I have a Quite Rare type.

HEMOCHROMATOSIS DNA, RESULT Homozygous Mutant Negative A
Homozygous for the H63D mutation and negative for the C282Y mutation in the HFE gene. Five percent of C282Y
homozygotes and rare H63D homozygotes develop clinical symptoms. Genetic counseling is recommended.

So more research, and I find only one other person in ten years

 https://www.. .nlm.nih.gov/pmc/articles/PMC4071918
https://www.. .nlm.nih.gov/pmc/articles/PMC4071918/

So with Multiple Sclerosis, I now am dealing with weekly phlebotomy, to try to rid myself of iron overload symptoms. the Gene center told All blood relatives needed contacted, as hereditary.

My blood comes out as thick or thicker than pancake batter.

  I think more studies need done, as I can not be the only one with MS, and Iron overload. Iron also effects the pituitary gland, so that tells me it crosses the brain barrier.
 Would love to know if anybody else has this rare H63d Gene, doing  phlebotomy,  and has MS.  How it effects MS, or any articles found.



Thanks for reading
JoeY

20 comments:

  1. Replies
    1. William, thanks for letting me know

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    2. William brown, have brother with MS, another brother with same mutated H63d/H63d hfe gene. His ferritin is 700. So something with genes, and your gut?

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    3. William,
      Did another article of gene testing. Everchangingms.blogspot.com

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  2. Yes, probably one of the first to give genetic testing. More blogs to follow, as see a Gene Specialists next week

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  4. Let me know how that goes. Which amino acids and shrooms? I stay quite low on iron, hemaglobin, and hematocrit six months later. Blood replenishment is every three months, so still concerned I have not bounced to a normal.

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  5. Would love to hear back. Only found 4 others that have both H63d genes that normally don't cause a problem, but did, by turning gene on. My Iron has not returned 9 months later. But has stumped my Cancer Dr. Adding iron pills or infusion would cause more problems of constipation. But back to cast iron pans.
    JoeY

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  8. Laurie and Julia,
    Interesting that this Dr can cure so much, while university Drs are always learning about MS. Figured if he had a cure, everyone would be cured.
    Some natural herbs are good, as I use them to help control MS, and the other neurodegenerative diseases that affect me.

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  10. Would love to hear more. My Iron never returned. Kept me in a anemia stage for a while

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  13. Does anyone still doubt natural herbs? I have seen the great importance of natural herbs and the wonderful work they have done in people's lives. I wonder why people still spend their money on English medicine when natural herbs can cure all kinds of mental diseases. I have seen it with my own eyes. My dad and aunt were cured from Huntington disease with Dr Bharet herbal medicine. He used BUJA herbal medicine to cure my dad and aunt from Huntington disease, I know it is hard to believe but am a living testimony. My dad was diagnosed with Huntington's disease in 2016, we have made use of all western medication yet no improvement and his doctors said there is no cure yet but still carrying out research, my dad experienced depression, anxiety and memory lapses that made him hallucinate always, he speaks to himself often and that made me shed tears each night that passes by. 2019 I searched through the internet for a solution and i came across a comment on a blog written by [Robert Jane] saying she was cured of Huntington disease that she suffered from for 8years. Without wasting time I quickly contacted Dr Bharat whose name was mentioned in the comment Via his email. He asked me questions which I answered correctly he sent his herbal medicine to us here in Ireland through DHL, in less than one month I started seeing positive improvement on my Dad's health so I introduced the medication to my aunt as well, is been 4 years now, my dad and aunt are living their best life again. Though i gave the medication as i was instructed. My dad and aunt are Huntington disease negative after the medication, Huntington disease is completely gone from my family lineage. With Bharat herbal medicine called BUJA Huntington patients can smile again. For those with Huntington disease or having their love ones diagnosed with Huntington's disease contact Dr Bharat now via dr.bharatkings@gmail.com you will come back to testify

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