If at first you don't succeed, try, try again. Then quit. There's no point in being a damn fool about it. -- W.C. Fields
I
had to laugh a bit when I first heard this quote. Thinking back on
all the hundreds of treatments I have tried and often continuously
repeated despite their ineffectiveness (and, at times,
counter-effectiveness), I sometimes have to wonder about myself. What
was I thinking?
But there is such a desperation and
overwhelming desire to get well that one will often try anything (and
keep at anything) in the undying hope of it suddenly working.
After
I became bedbound, I received a variety of nutritional IV's at home
twice weekly (sometimes daily) for about 4 years.... despite the fact
that they often made me feel worse. My doctor at the time (she is
no longer my doctor) told me that the ill effects were a result of
detoxification, and that I had to suffer through it in order to get
well. The biggest mistake patients made, she told me, was giving up
too early. I wanted to believe her so badly that I continued with
the treatments for years, hoping that, contrary to the evidence and my
own intuition, I was doing something which ultimately would benefit
me. In truth, I was also a bit limited in my choice of doctors. I
could find no other MD at the time to come to my house to see me and
thus felt I had little alternative but to listen to this doctor's
orders.
In the end, it turned out I should have
listened to my intuition. My reaction to the IV's was not detox; it
was my body's inability to tolerate the treatments. After watching a lecture by Dr. Paul Cheney,
a renowned ME/CFS expert, I learned that high dose vitamin C and
glutathione IVs can actually have a detrimental physiological effect
in some patients with ME/CFS. Not surprised by these findings, and
upon further research, I finally stopped the IVs.
The
pathology of ME/CFS is complicated and every patient reacts
differently to different therapies. I obviously don't want to deter
anyone who may be receiving a similar treatment and responding well to
it. I just wanted to make the point that I am not one to give up on
something very easily.
Though I'm doubtful to ever go
down such a road again, I always give any treatment a full-fledged
try, often for at least a year or longer. As with anything in life,
I've consistently wanted to make sure I gave it my all.
I've
received a lot of emails asking me if I've tried a variety of
therapies for ME/CFS, and I've therefore decided to do a quick run
down of some of the many things I have indeed attempted in my hopes
to get well. Please note that this is a very incomplete list and is
meant only as a general summary. I have been sick for over 13 years,
and to list all the things I've tried in that time would be too
enormous a task. So this is just a little overview. Exciting reading, I
know, but here goes ... :)
Prescriptions
A
growing list of antibiotics (Erythromycin, Cipro, Zithro, Doxy, IM
Penicillin, IM Rocephin, etc.), anti-virals (Acyclovir, Valcyte,
Valtrex, etc.), anti-fungal (Diflucan), anti-anxiety/anti-depressants
(purely to appease doctors; too many to name), anti-malarial
(Mepron), anti-coagulant (Heparin), stimulants (Ritalin, etc.),
thyroid/hormone replacement (including estrogen, progesterone,
testosterone and hydrocortisone), B12 shots (both hydroxy and
methyl), hepapressin, immune modulators (Isoprinosine), Florinef,
immune enhancers (immunoglobulins) and the like.
Alternative Therapies
Acupuncture,
massage therapy, shiatsu, jin shin jyutsu, energy healers,
herbalists/herbs, EAV/Asyra and electro dermal testing, live blood
analysis, visualization, cognitive behavioral therapy, stress
reduction/management, magnetic therapy, affirmations/positive thinking,
light GET/yoga and gentle lifting in bed with 1 lb ankle/wrist
weights (caused huge setback), hypnotherapy, reflexololgy, reiki,
detoxification, meditation, medical intuition, muscle testing, distance
healing, prayer, homeopathy, herbs, colonic (ugh!), 4+ years of IV
therapy (including Vitamin C, nutritional IV’s, amino acids,
glutathione, H202 and saline), oral chelation and a list of supplements
far too numerous to name.
Nutritional Therapies
As
noted above, I received a multitude of nutritional IV’s twice weekly
(sometimes daily) over several years. Almost all of them made me
worse. I’ve also tried a growing list of nutritional supplements that
likely exceeds well over 300 items. These include but are not limited
to vitamins, minerals, enzymes, amino acids, antioxidants, herbs,
probiotics, energy/nutritional/green drinks, Gookinaid, juicing, whey
protein, transfer factor, colloidal silver, cell food, chlorella,
mitochondrial supplements, mushrooms, immune enhancers/modulators, NT
factor, adrenal glandulars and the like, NADH, D-Ribose, and so on.
Diets
Elimination
diet (no gluten, sugar, dairy, wheat, etc), low carb diet, high
protein diet, low protein diet, paleo diet, raw food diet,
vegetarian, vegan, low sulfur, anti-candida, and a highly specific food
allergy elimination, etc.
Protocols
There
are several different ME/CFS and Lyme treatment protocols out there,
based on a variety of different theories, or on different aspects of
this complicated and multi-systemic disease. Some of the protocols I
have attempted include the Yasko protocol, the simplified
methylation protocol, the Patricia Kane protocol, the Dr. Zhang
protocol, Dr. Gupta's protocol (amygdala retraining), the Myhill
protocol (less a sauna), Dr. Martin Pall’s protocol, Cheney’s
protocol (prior to his recent change to CSF’s and stem cell
replacement), KPU protocol, and several other protocols I’m sure I am
forgetting.
Regarding the Marshall Protocol, I had
the proper testing done and it was determined (via a conversation
between my doctor and Dr. Marshall himself) that I would not be a
good candidate.
Doctors I've Seen
As
for the various types of doctors I've seen over the years, they
include about 5 internists, 3 infectious disease MD's, a neurologist, a
rheumatologist, an endocrinologist, 2 dermatologists (for hair
loss), an allergist, several naturopaths, a world renowned
integrative medicine MD, 3 acupuncturists, 2 herbalists, 2
nutritionists, a psychotherapist specializing in chronic illness, a
cognitive behaviorist, and multiple alternative health practitioners.
Whew!
So, there you have my partial list. Though few of the treatments
have really helped me, I suddenly feel like I've been very busy all
these years. :)
As for my current regimen, it
includes a healthy diet, meditation, an antiviral, medications to
help with sleep, natural thyroid, Equilibrant, Hydroxy B12 shots, the
KPU protocol, light stretching in bed, and about 20 different
supplements. I am also attempting LDN (low dose Naltrexone) and a
nutritional immune modulating powder called Avemar.
Here's
hoping that new and better treatments are around the corner for us
all. If nothing else, there's no doubt we will all still continue to
try, try again...
Saturday, February 27, 2010
Thursday, February 18, 2010
The F Word
So, I’ve been thinking of the F word lately. Not that F word, but the other one.. the one in the acronym of CFS/CFIDS. That dreaded word fatigue.
In the thick of a long standing crash, it strikes me even more deeply just how grossly inadequate a term it is for what we experience. In Hillary Johnson's Osler's Web, Dr. Mark Loveless was quoted as saying that, at their worst, "the CFIDS patient feels every day significantly the same way an AIDS patient feels two months before death.” If I were to try to capture such a feeling in a word, I’m not sure what I would use, but it wouldn’t be fatigue.
The eloquent Ms. Laura Hillenbrand (author of the best-seller Seabiscuit and long time sufferer of CFS) put it this way: “This illness is to fatigue what a nuclear bomb is to a match. It’s an absurd mischaracterization." Indeed.
As I was contemplating this frustrating word one morning, I wanted to attempt to give it a bit more weight and power somehow. In the process, I ended up with the idea for the following... well, poem of sorts. Please bear with me here. I have not written more than a couple poems since I was a child. This is an amateur attempt at best, but I wanted to share it anyway because this word is so often misused in relation to our disease.
F is for fierce, ferocious, feverish fatigue, it's
Flamed fingers folding over you, filling you with its
Feral, filthy fumes until you fall face forward,
Fallowed from its forbidding force. Your
Former self, physically now so fragile and frail,
Falters and fumbles, yet…
Fervently forges
Forward
Fighting for a
Fleeting flicker of freedom.
F is for the felicity of fabulous fantasies that
Float effortlessly in the fluidity of dreams,
Fearlessly and faithfully flourishing in flight,
Foretelling a
Future
Fully
Fortified
Functional
Fruitful
Full-bodied
and
Finally
Fervently
Free…
--LB © 2009
See how the poem is in... the shape.. of an F? And I used mostly all F words? Hello? Anyone? ;) Okay, a bit forced, but I tried. :)
Thanks to all those who left such wonderful comments of support and encouragement to me with my last post. It was so appreciated. Regretfully, my crash continues and has not yet fully abated. It's been a very rough few months, to say the least. I'm a bit concerned this may be my new CFS "normal," but I'm trying to remain as patient as possible, and as always, I continue to hope.
In the thick of a long standing crash, it strikes me even more deeply just how grossly inadequate a term it is for what we experience. In Hillary Johnson's Osler's Web, Dr. Mark Loveless was quoted as saying that, at their worst, "the CFIDS patient feels every day significantly the same way an AIDS patient feels two months before death.” If I were to try to capture such a feeling in a word, I’m not sure what I would use, but it wouldn’t be fatigue.
The eloquent Ms. Laura Hillenbrand (author of the best-seller Seabiscuit and long time sufferer of CFS) put it this way: “This illness is to fatigue what a nuclear bomb is to a match. It’s an absurd mischaracterization." Indeed.
As I was contemplating this frustrating word one morning, I wanted to attempt to give it a bit more weight and power somehow. In the process, I ended up with the idea for the following... well, poem of sorts. Please bear with me here. I have not written more than a couple poems since I was a child. This is an amateur attempt at best, but I wanted to share it anyway because this word is so often misused in relation to our disease.
F is for fierce, ferocious, feverish fatigue, it's
Flamed fingers folding over you, filling you with its
Feral, filthy fumes until you fall face forward,
Fallowed from its forbidding force. Your
Former self, physically now so fragile and frail,
Falters and fumbles, yet…
Fervently forges
Forward
Fighting for a
Fleeting flicker of freedom.
F is for the felicity of fabulous fantasies that
Float effortlessly in the fluidity of dreams,
Fearlessly and faithfully flourishing in flight,
Foretelling a
Future
Fully
Fortified
Functional
Fruitful
Full-bodied
and
Finally
Fervently
Free…
--LB © 2009
See how the poem is in... the shape.. of an F? And I used mostly all F words? Hello? Anyone? ;) Okay, a bit forced, but I tried. :)
Thanks to all those who left such wonderful comments of support and encouragement to me with my last post. It was so appreciated. Regretfully, my crash continues and has not yet fully abated. It's been a very rough few months, to say the least. I'm a bit concerned this may be my new CFS "normal," but I'm trying to remain as patient as possible, and as always, I continue to hope.
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