So I thought that I would reproduce the piece below, for your information. Thanks to Hpathy.com for publishing this historical document - and demonstrating how timeless homeopathy is.
Asthma and Homeopathy

So I thought that I would reproduce the piece below, for your information. Thanks to Hpathy.com for publishing this historical document - and demonstrating how timeless homeopathy is.
Mums, Pregnancy and Homeopathy

As WDDTY have said recently, there is no such thing as a safe drug for a pregnant woman, and virtually every prescription drug could cause birth defects. Yet as they go on to say, doctors are prescribing an ever-increasing number of drugs to women, often ignoring official warnings. This is according to a recently published survey that discovered many women were taking up to 4 different drugs. The survey found that 80% of pregnant women were taking some form of drug, an increase of 60% over the past 30 years.
Clearly, the drug companies, GPs, and the entire Conventional Health Establishment has learnt little since Thalidomide!
The study was done by researchers from Boston University Stone Epidemiology Centre, after reviewing a survey of 30,000 women. (Source: American Journal of Obstetrics and Gynecology, 2011; doi: 10.1016/j.ajog.2011.02.029).
The WDDTY feature is at
http://www.wddty.com/doctors-giving-drugs-to-half-of-all-pregnant-women-despite-the-warnings.html
and it is interesting to see their previous articles on this subject. They include articles on antibiotics causing birth defects, Prozac babies have birth defects, Antidepressant drugs cause birth defects, Fertility drugs and birth defects. And one that comes to this conclusion:
"Women who are very young or pregnant are two population groups who should almost never be prescribed general pharmaceuticals.
WDDTY are doing a great service in warning us all about the dangers of pharmaceutical drugs at this critical time. But rather than worrying, mums should relax, and get in touch with a local homeopath to make sure she has safe treatment available to her should she need medical treatment.
D Blog Week, Day Two: Dear Diabetes Guilt

Diabetes guilt isn't type specific. Type 1, type 1.5, type 2, or type 3,we've all experienced it ~
Assignment number two for Diabetes blog week was to write a letter to your diabetes, or a person, place, thing associated with your diabetes. SO glad Karen picked this as a topic! I'm a HUGE fan of writing a letter to my diabetes, and even have a " Dear Diabetes" label on my blog that currently has close to 4 dozen letters.
I find writing a personal letter to or about diabetes incredibly cathartic, healing, and down right cool and I HIGHLY suggest you try it if you haven't already!
The following letter: Dear Diabetes Guilt, was original posted on October 27th, 2009, after a discussion I participated in about guilt and chronic illness on twitter.
I was all set to write a new letter last week, but after noticing lots of blogs from type 1s, 1.5s, type 2s and type 3s regarding the subject of diabetes guilt, I felt that it was appropriate to repost this one.
And it's my hope that you take something positive away from it~
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Dear Diabetes Guilt:
You’ve been with me and by my side almost daily since my diagnoses.
I first experienced you when I looked into my parents’ eyes when I was diagnosed and saw the sadness that was looking back at me. I was child number 6, diabetic child number 3.
My diagnoses hurt my parents so much. All I could say was “I’m sorry”- and then I did my best to make them laugh.
The guilt was next me as I snuck Christmas Cookies from the freezer and blamed the cookies disappearance on my sister- child number 3, diabetic child number 2.
Diabetes, your guilt made a 10 year old little girl run laps around the block to burn off contraband Reese’s Peanut Butter Cups.
Diabetes guilt (and the look of disappointment and fear in my parents eyes) made me lie to them regarding my urine testing and blood sugar results.
It wasn’t the high numbers I was afraid of- it was making my parents sad, scared and angry that made my 11-year-old self fudge my numbers.
I'd cry when my Endo told me I wasn't trying hard enough. I was 13 and doing my best.
Wanting a few cookies every now and then shouldn't have equated a trip to confession and 13 "Hail Mary's".
In high school you mocked me to be part of the crowd - but I couldn't ignore diabetes.
Between the hell that was high school and being a PWD, it was a long 4 years.
In college I felt your guilt daily. I wanted too fit in and be “normal, ” and having diabetes was a foreign routine on campus.
I used my humor to win friends and they accepted both diabetes and me, as is.
I flourished with friends and success.
Your guilt didn’t just affect me-It damaged my family as a whole.
Your guilt cursed my sister- She strived for normalcy – which eluded her because back in the diabetes dark ages, normal was never an option.
I felt diabetes guilt because my sister with diabetes was dying and I was angry with both her and the world.
I didn’t understand how sick she was or how much the guilt of diabetes drove her down a self-destructive path.
I just knew she was sick and that I spent so many of much of my high school and college years taking care of her with my parents.
I didn’t understand and I hate to admit now, but I blamed her for not taking better care of herself.
I was a kid, she was 14 years older than me, and I didn’t understand what a restrictive world she and her diabetes were brought up in until I was well into adulthood.
If my other sister (child number 1, diabetic number 1) could live good life and have three healthy sons, why couldn't she?
I felt diabetes guilt for not always understanding, and for always being fearful that it could have been me.
I wanted to be a full time college student. Not a full time college student who was a PWD and a caretaker as well.
Even thought we fought as only siblings can, I never thought that diabetes complications would actually kill her.
I felt guilt for not having patience and for not always being kind.
My diabetes guilt stood beside me as I gave her eulogy.
I felt your guilt whenever people spoke of how much my sister suffered.
I felt your guilt whenever I got my own test results back.
I felt your guilt in my mid twenties when I was scared into becoming a good patient.
In my mid twenties and early thirties I worked hard on my diabetes management and had the numbers to prove it.
My Dr. went so far as to call me a model patient.
But still, your guilty presence made me want to apologize all the time- even when I was doing nothing wrong.
When I contemplated a cupcake, I felt guilty. Even when I tested, counted carbs, and bolused accordingly.
I apologized whenever my numbers would go up or down for no apparent reason.
I became defensive whenever a friend would ask: Kel, should you eat that?
I’d feel guilty that I don’t excise enough and I’d feel guilty when I exercised to much and would run low because I’d miscalculated my temporary basal rate.
Over the past 15 years I’ve learned to only concentrate on one number at a time.
I owe that attitude (in part) to you.
Because I became so tired of having you as a companion and a partner in my diabetes management.
So I’ve learned (and am still learning every day) to let go of you.
I accept that you exist and I will admit that you’ve done some good.
But I grew so tired of having you as the anchor I wear around my neck.
So, I removed you from my world on a daily basis - and while you still make your presence known from time to time, I no longer say I’m sorry for being a human with Diabetes.
I've lifted your anchor of guilt, hitched up my sails in the wind, and let my diabetes flag fly!
I have my good numbers and my bad.
I have great test results, and some not so great ones from time to time.
But I always try, and try again.
When I fall off the diabetes wagon, I get up and get back on.
Instead of anchoring on to the guilt, I use those numbers and results as a GPS in my diabetes management.
I take it one number at a time and I always do my best.
I own my diabetes, diabetes doesn't own me.
I’m still sorry that diabetes exists in the world.
But I am no longer sorry for being a person with Diabetes.
A Typical Day In Living A Life With Diabetes???

Hmmm, not as easy as it sounds. Diabetes is never the same disease two days in row. What works for me on Monday, might not work for me on Tuesday, even if my blood sugar numbers and activities are similar.
Life with the Big D is a balancing act requiring us to precariously balance blood sugar numbers - both high and low, carbs, ratios, activities, doorknobs attracting pump tubing, the occasional appearance of ketones, and the every so sneaky attack known as Murphy's Law.
I've written the analogy before, life with diabetes is a circus of sorts, a theater of both the absurd and required. And like all good theater, every performance is slightly different.
A typical day requires me to jump through diabetes hoops and be flexible and diligent at the same time.
And every day, typical or not, requires me to test my blood sugars, over and over, and over and over, and over and over, and over and over and over and over, and over and over, and over and over again.
A typical day requires me to triple check my work bag to make sure I have back ups of everything. And by everything I mean; pump supplies, test strips, lancets- OK, who am I kidding? I may bring back up lancets, but I rarely use them. Back to the check list, extra insulin, two Lara bars, pump batteries, and a penny- not for luck, but to unscrew the lid on my pump so I can replace the battery.
On any given day, I know that when I least expect it I'll run into a Cappo in the Diabetes Police who will lecture me (for my own good of course,) on Diabetes management, etiquette, and the likes there of - and will most certainly get it wrong. I prep myself to keep my cool, except of course, when I throw caution to the wind and my "cool" out the window and rip said Diabetes Police a new one!
And lastly, I prepare myself on a daily basis to expect both the expected and the unexpected- and roll with it. Because by rolling with the diabetes tide instead of against it, I not only keep what little sanity I have left, but end up with the diabetes upper hand....at least for the moment at hand~
Asthma at epidemic levels - is it caused by pharmaceutical drugs?

- In 2000, GP's in the UK saw over 18,000 cases relating to new asthma attacks each week.
- The number of new cases of asthma each year is now 3 to 4 times higher in adults and 6 times higher in children than it was 25 years ago.
- Of 56 countries surveyed, the UK has the fifth highest prevalence rate (20.7%) for asthma in 13 to 14 year olds.
- Asthma attacks now cost the UK an estimated £1.2 billion in lost productivity, £850 million in NHS treatment and a further £161 million in social security costs.
- Over 18 million working days are lost to asthma each year
- 5.2 million people in the UK are currently receiving treatment for asthma: this includes 1.1 million children (1 in 10 children) and 4.1 million adults (1 in 12 adults).
- There is a person with asthma in one in five households in the UK.
- There were 1,381 deaths from asthma in the UK in 2004 (40 were children aged 14 years or under). On average, 4 people per day or 1 person every 6 hours dies from asthma.
- An estimated 75% of hospital admissions for asthma are avoidable and as many as 90% of the deaths from asthma are preventable.
- 42% of people with asthma say that traffic fumes stop them walking and shopping in congested areas
- 40% of people with asthma avoid smoky pubs and restaurants
- 56% of people with asthma are sensitive to pet allergens
The Health Debate (4). The cost-effectiveness of Big Pharma drugs

We also have a situation where the numbers of people suffering from chronic diseases, like Arthritis, Cancers of all types, Dementia, Depression, Autism, and disease linked to heart, kidneys, liver, have all increased, often exponentially.
We suffer chronic disease now at epidemic levels. Why? Why is it not discussed?
If we then consider (just) the known, and admitted side-effects, adverse reactions, and disease-inducing effects (DIEs) of Big Pharma drugs, the link between increased expenditure on conventional medical (ConMed) treatment (largely drug based) and increasing costs becomes clear.
But, of course, this essential feature of the 'health debate' is rarely discussed by the mainstream Media. Nor is the performance of ConMed ever compared with other medical therapies, like homeopathy.
Why is this? And what kind of questions should the Media be asking if it had any intention of entering into "the Health Debate"? Perhaps these are just of few of them!
- Why does the Media not ask searching questions about why Big Pharma drugs are so excessively expensive?
- Why does the Media not focus on either or both side of the 'cost-effectiveness' question when it comes to ConMed drugs?
- Why does the Media not ask questions about the link between increasing NHS expenditure, especially on Big Pharma drugs, and the rising levels of chronic disease?
- Why has the NHS conducted so few comparative studies on the cost-effectiveness of ConMed, Homeopathy, and other CAM therapies?
- Why are NHS resources spent almost totally on one medical discipline, ConMed? Why does the NHS not spend more money on Homeopathy, and other CAM therapies?
- Why, despite massive annual increases in NHS spending in recent years, are ConMed health services still overstretched, and often, apparently, quite unable to cope with the demands of ill-health and disease?
Dementia / Alzheimer's Disease. Caused by conventional medical drugs?

- There are currently 700,000 people with dementia in the UK.
- There are currently 15,000 younger people with dementia in the UK (considered to be an under-estimate by about 3-times as data relies on referrals to services).
- There are over 11,500 people with dementia from black and minority ethnic groups in the UK.
- There will be over a million people with dementia by 2025.
- Two thirds of people with dementia are women.
- The proportion of people with dementia doubles for every 5 year age group. One third of people over 95 have dementia.
- 60,000 deaths a year are directly attributable to dementia.
- The financial cost of dementia to the UK is over £17 billion a year.
- Family carers of people with dementia save the UK over £6 billion a year.
- 64% of people living in care homes have a form of dementia.
- Two thirds of people with dementia live in the community while one third live in a care home.