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How I cured my Chronic Fatigue Syndrome virtually overnight

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Chronic Fatigue Syndrome
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From Toronto
New Member
Joined : Aug 2014
Posts : 3
Posted 8/18/2014 12:14 PM (GMT -6)
Let me just say I'm a 38 yr old male, I been suffering from CFIDS for almost 15 yrs now.
This is a very frustrating disease. You go through periods where you'll feel well, then you'll go out and play some sports, and the next day you are so exhausted you cannot get out of bed.

So how did I cure myself?? Well, it wasnt by going to doctors, although they were helpful here and there.
But to cure yourself you most likely wont get it from a pharma script, at least that was the case with me. You need it from a natural source.

Every CFIDS is different, so I can't guarantee this will work for everyone. If you have Lyme disease this may not work. But it might help some people who are going through the same thing I was going.

The main reason why people suffer from CFIDS is because their hormonal system is out of whack.
Hormone comes from the Greek term meaning “to spur on”. If your body isnt producing hormones at an optimum level, you will most likely have very little energy and feel tired all the time.

The master hormone gland in your body is the Hypothalamus gland. It controls the pituitary, adrenal, thyroid and all other sex hormone glands. Anyone who has CFIDS will tell you besides feeling tired all the time, they also probably dont feel like having sex very much.

So how do you fix your hypothalamus gland if its not functioning properly??! Real simple answer. You take a hypothalamus glandular capsule or pill once or twice a day. There are only a handful companies who sell hypothalamus glands in North-America. They should come in strengths of 500 mg. You take 1 or 2 of these a day, and within hours you'll start to feel your energy building up again.

To get the full benefit you need to take it for a few months. Then when your body has recovered you can gradually wean yourself off by cutting capsules in half, or even down to 1/3 a capsule.

You can also after a few weeks add adrenal glandulars, pituitary and/or thyroid glandulars to see if that makes a difference. I did notice my recovery went a bit quicker when I added the adrenal glandular.

All these glandulars are available on "google shopping" for a reasonable price.

One of the theories out there why so many women get CFIDS is because in some women the contraceptive pill can throw your hypothalamus out of whack if you take the pill for a long time. But that is just a theory so far, no scientific proof

15 years I suffered with this disease. I'm glad I finally kicked it to the curb :-)



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Post Edited (From Toronto) : 8/18/2014 12:23:14 PM (GMT-6)

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Wackers34
Veteran Member
Joined : Apr 2013
Posts : 694
Posted 8/22/2014 12:46 PM (GMT -6)
this is ineresting...I have had this 19 months now and have tried everything...but just started on an adrenal protocol. I have tried glandulars but they did not agree with me and caused severe stomach problems...i now take adrenal assist with all natural help in it for adrenals - this along with clean diet and other supps is actually starting to slowly help me...Im hearing of more and more people helping their CFS though and this really pleases me :)
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From Toronto
New Member
Joined : Aug 2014
Posts : 3
Posted 8/22/2014 2:11 PM (GMT -6)
I got CFS right after I was prescribed cortisone pills for an eczema skin condition I had. My theory is the cortisone (which is a hormone pill) threw my hypothalamus and adrenal glands out of whack.

It even says right on the official drugs.com website that cortisone can depress the hypothalamus-pituitary-adrenal axis. In my case that axis never quite returned to normal, and the only way to fix it was by taking the glandular pills.

See here: http://www.drugs.com/sfx/hydrocortisone-side-effects.html

Long-term effects have included hypothalamus-pituitary-adrenal activity suppression, Cushingoid appearance, hirsutism or virilism, impotence, menstrual irregularities, peptic ulcer disease, cataracts and increased intraocular pressure/glaucoma, myopathy, osteoporosis, and vertebral compression fractures



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Post Edited (From Toronto) : 8/22/2014 2:16:31 PM (GMT-6)

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pmus2018
New Member
Joined : Jun 2018
Posts : 1
Posted 6/15/2020 5:11 AM (GMT -6)
Hey 'From Toronto'. Your post struck a chord with my situation as I am giving Hypothalamus glandular a try. How have things been since this post? Have you continued taking glandulars? Thanx
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Earfboii
New Member
Joined : Nov 2020
Posts : 5
Posted 11/20/2020 6:00 PM (GMT -6)
Very interesting. I got worse after a course of prednisone. What kind of glandular pills did you guys take?
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