What Do They Want?

Preparing for my vitamin IV on Wednesday.  They call it the "pick me up"... I'd say so!  I felt fabulous for the past 4 days.

Preparing for my vitamin IV on Wednesday. They call it the “pick me up”… I’d say so! I felt fabulous for the past 4 days.

I’ve felt written off and passed around from specialist to specialist with “no answers” worthy to chart – while clearly the answers seem very obvious to me to the whole time…

I almost have felt sorry for doctors, who rely so heavily on these blood tests for answers… and the patients who so desperately want to know what is going on so they can be well.  I wonder if they would change how they did things, if they truly knew how much nutrition played into things…

Those videos I mentioned the last week… that doctor said when he went back to his original group practice – eager to help his patients get off of their medicines, and transform their lives, so their bodies could naturally heal – as God intended….

Most didn’t want to hear it.

They didn’t want to change.

They couldn’t afford any test that was out-of-pocket, and not covered by insurance… and often insisted they would rather have their prescription medicine, which WAS paid for by their insurance.

How sad that the things and people who can actually make us well, are NOT paid for by our insurance?  What is wrong with our country???

Do you know who pays for many of the studies that are done at hospitals… in the name of “advancing medicine”???

It’s the drug companies.

Do you think they’re looking out for your well-being above all?  Or are they concerned with the bottom line, and selling products?

I noted that even the Chicago University Celiac Center was privately funded…   and I thought – wow, that’s strange – when 97% of people aren’t diagnosed, you would think there would be money to FUND such an important illness.

But alas, you can’t own the rights to “proper nutrition”… and you can’t sell whole food vitamins in a patented format that would be a money-maker to the drug companies and medical doctors alike.

Food companies have gotten on board to fund some of the “search for a cure”… but  still don’t quite understand that – when the cure is – avoiding the foods that make us sick?

I have also read some of the “negatives” about holistic medicine.   That they want to sell you “their” supplements… Well for one, that has NOT been my experience.  They have been VERY open with what I need – but never pushing me to buy things only “from them.”

Secondly, this low dose Armour I’m on for my thyroid…  which most endocrinologists poo-poo.  The sheet on the prescription states it has “no” negative side effects.  Interesting…  I wonder what the list is on Synthyroid??  Why again won’t doctors give it a chance if a patient is wanting it?  Oh yes… that’s right – it’s not the money-maker, and perhaps you wouldn’t need it forever like you do Synthyroid?

Now, I realize – not all doctors are like this, and there are just as many out there that have no clue that they are making choices that have really bad consequences for their patients.  I still shake my head when I think of my GI doctors telling me he would prescribe me some anti diarrhea medicine, following my endoscopy.  Knowing that would have only masked things until I probably ended up with colon cancer, or continued poisoning my system with more auto immune disease issues searching for anything else, since “a professional” told me that wasn’t the problem.  While he was a professional, he was professionally wrong in my case.

I look forward to sharing with you our latest decisions we need to make.  We got two phone calls last week – one indicating my blood work from the learning hospital showed my ANA is up again.  Now it’s 1:320.  I was referred to a rheumatolgist… that I can’t decide if I’d like to see.  What are they REALLY going to be able to do?  Do I really need a diagnosis in my chart?

Another call was from an immunologist specialist my son visited 2 weeks ago… His grand plan of vaccines, medicines and testing made my head hurt… that was before I got his paperwork, where the doctor stated some elements of my son’s health history MAJORLY incorrect.  Chicago University did the same thing – I simply don’t think listening nor knowledge on nutrition and health is the strong suit.  I’m thankful we live in America and have choices… This boy needs help with his immune system, and has made great strides already, since last May.  He does not need more medicine and doctors appointments.

I’ve continued to feel well this week after my vitamin IV, and additional supplements.  I had a bit of systemic pain today – in the morning and evening yesterday, with some fatigue…but I was also on my feet most of the day.  I fought back and did an hour-long DVD with Bob Harper tonight.  Bob always makes me laugh.  I needed that.  I’ve done one of those a week now… which is a huge progress for me since September.  Praise God.

Please.  Educate yourself as much as you can about nutrition and the symptoms you have if you are sick with auto immune disease, cancer, asthma or thyroid or other hormone issues… we truly ARE what we eat – and genetically it’s effecting our country in a BIG way.

“This is the day the Lord has made; let us rejoice and be glad in it.”

Psalm 118:24

Posted on January 27, 2013, in Celiac/Gluten Sensitivity, Change, Diet, Label Reading, Metabolism, Our Struggles and tagged , , , , , , , , , , . Bookmark the permalink. 1 Comment.

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