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Re: FMS--Dr. Lowe

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marie

Your story is just what I am afraid of would happen to me. That is

why I have not pursued the thyroid thing. I have fms and certainly

have several sympoms of low thyroid, but I am thin and have normal

thryroid tests. I also had lots of heart palpatations before I got

explanted. I am afraid as sensitive as I am to everything, I would

get a bad reaction to meds. On the otherhand, if it was my problem

and that helped it would be so great. So at this point, I am sitting

on the fence

kathy

-- In , Jane Doe <oceanlilly_csu@y...> wrote:

> and All:

> Dr. Lowe's site is very interesting.

>

> I am a believer that one can have hypothyroidism and be in the TSH

" normal range " .I know a few women who had TSHs between 3.0-4.0

(technically in that normal range) who's lives/health have improved

greatly with appropriate thyroid meds. So there is no doubt that

physicians need to think outside the box when it comes to thyroid

therapy--and all conditions for that matter.

>

> I would also agree with Lowe that if a patient exhibits

signs/symptoms of hypothyroidism a carefully monitored (telling

patients what harmful side effects may occur) trial run of thyroid

therapy would be warranted providing the doctor goes about this

therapy and exercises great caution. If a patient's body rejects a

very low doses of meds, their body does not need this thyroid

medication and the therapy should cease at this point.The problem is

with some dangerous practitioners out there, this is not always the

case: they " force " thyroid meds on folks and this often results in

trips to the ER or even worse--death (as in the case litigated

in Fla.).

>

> I made the near fatal mistake of going to a " type " MD and he

tried to " force " my body to " accept " thyroid meds it clearly did not

want. I could have died. After just consuming a half grain T3 T4 for

two days, then dropping down to a 1/4 for five days, I ended up in the ER.

> When my symptoms first began--nearly straight away, I had contacted

this doc immediately with symptoms of heart palps, bone-growing

sensation, eyeball popping sensation, extreme jitters and shakes,

shortness of breath, inability to sit still or sleep.He told me to

take Xanax and allow my body to " except " the thyroid meds. His belief

is the " popular " belief than any TSH over 2.0 is hypothyroidism. I had

dry skin, hair loss from surgery so he took a leap from that and

decided I was hypothyroid.Very shallow thinking, not to mention dangerous.

>

> If anyone's thyroid is normal or not, know the signs of going hyper

BEFORE beginning any thyroid treatment. If you react badly to a low

LOW does of T3 and/or T4, chances are you never needed the meds to

begin with. It is worth trying to rule out this disease--just be

careful to avoid the hoopla and take only YOUR individual situation

into account because your life may very well depend on it as mine did

and other people I know who were wrongfully diagnosed/medicated. A

good doctor will be very careful and proceed with EXTREME CAUTION.

>

> Have your thyroid checked regularly.

> LM

>

> JOSEPH PALANCA <juliejp61@m...> wrote:

>

> I was told i had FMS, as I had all aymptoms, and 11 of the 18

trigger points by a rheumy and a chiropracter. I was told this with my

implants in, and shortly after. Since doing Dr Lowe's metabolic

program www.drlowe.com with higher thyroid meds(esp t3) to overcome

cellular resitance, and myofasial massage to the tender points by a

chiro- almost all fms sympotoms are gone, and I only have two tender

points left. Dr Lowe believes most FMS cases are due to under

regulation of thyroid hormones, whether or not blood work shows it.He

has a huge wellness center based on Fibromyalgia, and has dealt with

FMS for years, and written two books on metabolic issues and FMS. If

you have FMS, I would just look into it, very informative.

>

>

>

>

>

>

> >From: jaylow2100@a... >Reply- >To:

>Subject: Re: Re:

FMS-- >Date: Wed, 11 Aug 2004 12:08:23 EDT > >Hi , >

>I have a pretty bad case of FMS but am slowly getting better. It came

on >strong about two years ago right before I had my implants out.

Since then I have >been up and down with it. Somedays I am in a lot of

pain and some days not >so bad. I am currently getting a pretty wierd

treatment but it seems to be >working better than anything else I have

done. I have detoxed to the max. > >I am now getting bee venom

treatments. I am lucky to have a practioner here >that does it. She

takes out the stinger from bees and gently taps them into >different

acupuncture points. The venom (also the pollen, royal jelly and

>propolis) all have strong anti inflammatory properties and strong

anti bacterial, >anti viral and anti fungal properties as well. I did

some research and this >has been used as a

> treatment for arthritis and rhuematism for centuries. It >was used

extensively in the US before the advent of steroids. > >My lady went

to Japan to study this treatment BUT there are apitheripists all >over

the country who will give you bee venom treatments. If you go on line

>you can find them through the apitherapy website. I have had three

treatment >so far and feel a lot less achy and the extreme back pain

has lessened >considerably. I am going to go for at least three

months. This lady treats a lot of >MS patients and says that it takes

a long time but some actually go into >remission. > >I have talked to

a few of her FMS patients and they say they have improved >immensely.

>You have to make sure you are not allergic to bees though before you

start. I >feel good about this because it is totally natural and does

not have the side >effects of anti inflammatory pain drugs and

steroids. > >Love to all, >Judi L

>

>

>

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