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My Experience with Human Growth Hormone

My fibromyalgia was severely aggravated by an accident in January of 1997.  It got so bad, that I had flares, including fever, aches and severe pain, several times per week.  I missed many days at work and was severely depressed.  I became so weak that I couldn't walk up a flight of stairs without feeling like I was going to collapse. I caught every cold and flu that came along.  Then, I was told about human growth hormone (HGH) and, like some many other things that were "supposed" to help me, I was hesitant to try it because I couldn't bear another disappointment.  I had hoped that, at least, it would prevent me from getting so many colds and infections.  I began taking it May 29, 1999 and, in less than a week, my energy level had significantly increased.  By the second week, I could run up a flight of stairs without huffing and puffing.  I did not have a single flare in almost 8 weeks until July 23, 1999, after suffering from major emotional trauma.  However, by the next day, the flare had resolved.  I have never been so impressed with a product before in my life.  I am so impressed, that I'm now selling the product so that other people can, hopefully, get relief.  We are now in the height of allergy season and I haven't taken medication.  I cannot guarantee that it will work this well on you or on your friend or family member with fibromyalgia.  All I want to do is to share my experience and hope that other people will benefit from this wonderful product.

 

Clinical Supporting Evidence for My Results
TITLE: Disordered growth hormone secretion in fibromyalgia: a review of recent findings and a hypothesized etiology.
AUTHORS: Bennett RM
AUTHOR AFFILIATION: Dept. Medicine (L329A), Oregon Health Sciences University, Portland 97201, USA.
SOURCE: Z Rheumatol 1998;57 Suppl 2:72-6
CITATION IDS: PMID: 10025088 UI: 99149227
ABSTRACT: Growth hormone (GH) deficiency occurs in about 30% of fibromyalgia patients. Treatment of GH deficient fibromyalgia patients with recombinant growth hormone improves several clinical features, including the tender point count. Defective GH secretion in these patients appears to be due to increased somatostatin tone in the hypothalamus. An hypothesis is presented which relates dysfunctional GH secretion to the effects of intermittent hypercortisolemia on upregulating the density of beta-adrenergic receptors in the hypothalamus. The resulting augmentation of beta-adrenergic tone stimulates the release of somatostatin, thus, impairing GH secretion.

TITLE: A randomized, double-blind, placebo-controlled study of growth hormone in the treatment of fibromyalgia.
AUTHORS: Bennett RM; Clark SC; Walczyk J
AUTHOR AFFILIATION: Department of Medicine, Oregon Health Sciences University, Portland 97201, USA.
SOURCE: Am J Med 1998 Mar;104(3):227-31
CITATION IDS: PMID: 9552084 UI: 98211811
ABSTRACT: PURPOSE: The cause of fibromyalgia (FM) is not known. Low levels of insulin-like growth factor 1 (IGF-1), a surrogate marker for low growth hormone (GH) secretion, occur in about one third of patients who have many clinical features of growth hormone deficiency, such as diminished energy, dysphoria, impaired cognition, poor general health, reduced exercise capacity, muscle weakness, and cold intolerance. To determine whether suboptimal growth hormone production could be relevant to the symptomatology of fibromyalgia, we assessed the clinical effects of treatment with growth hormone. METHODS: Fifty women with fibromyalgia and low IGF-1 levels were enrolled in a randomized, placebo-controlled, double-blind study of 9 months' duration. They gave themselves daily subcutaneous injections of growth hormone or placebo. Two outcome measures--the Fibromyalgia Impact Questionnaire and the number of fibromyalgia tender points-were evaluated at 3-monthly intervals by a blinded investigator. An unblinded investigator reviewed the IGF-1 results monthly and adjusted the growth hormone dose to achieve an IGF- 1 level of about 250 ng/mL. RESULTS: Daily growth hormone injections resulted in a prompt and sustained increase in IGF-1 levels. The treatment (n=22) group showed a significant improvement over the placebo group (n=23) at 9 months in both the Fibromyalgia Impact Questionnaire score (P <0.04) and the tender point score (P <0.03). Fifteen subjects in the growth hormone group and 6 subjects in the control group experienced a global improvement (P <0.02). There was a delayed response to therapy, with most patients experiencing improvement at the 6-month mark. After discontinuing growth hormone, patients experienced a worsening of symptoms. Carpal tunnel symptoms were more prevalent in the growth hormone group (7 versus 1); no other adverse events were more common in this group. CONCLUSIONS: Women with fibromyalgia and low IGF-1 levels experienced an improvement in their overall symptomatology and number of tender points after 9 months of daily growth hormone therapy. This suggests that a secondary growth hormone deficiency may be responsible for some of the symptoms of fibromyalgia.

 

 

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