Jump to content
RemedySpot.com

karen

Rate this topic


Guest guest

Recommended Posts

,

Selenium is notoriously low in UK soils.

karen

asd adults i know with pronounced response to selenium are from

canada and tasmania both selenium deficent areas...

so i can't exactly know how it will be for you since i don't know

your selenium intake from food...

i reckon you should really notice something with three weeks/one

month max.

your posts indicate decreasing mercury toxicty

Link to comment
Share on other sites

mercury in the fish, low selenium, amalgams....

north scotland is so asd ....

puffins up ther to...

> ,

>

> Selenium is notoriously low in UK soils.

>

>

> karen

>

>

> asd adults i know with pronounced response to selenium are from

> canada and tasmania both selenium deficent areas...

>

> so i can't exactly know how it will be for you since i don't know

> your selenium intake from food...

>

> i reckon you should really notice something with three weeks/one

> month max.

>

> your posts indicate decreasing mercury toxicty

>

>

>

>

>

>

Link to comment
Share on other sites

  • 6 months later...
Guest guest

, I agree with Jan & others. You have to somehow get these bozo's to agree on who will be head clown. My doc's can be like this and the head clown in my case seems to be the Head transplant coordination who is a nurse practitioner. All the docs clear everything through her. She is not really a clown, she takes her job seriously and keeps my med list up to date on her computer. I am fortunate to have her. Find someone to do this. Maybe it will be someone at Vanderbilt.

I have been in the situation where I have been in pain and didn't know who to go to. I don't know your situation but seems like your PCP should be making sure you are getting the right care.

Take care & good luck

Patty

-----Original Message-----From: Ian & Janet [mailto:ianjanaust@...] Sent: Wednesday, June 04, 2003 1:09 AM Subject: [ ] KAREN

......dont hesitate go to the ER.....gosh I feel so sorry for you, when youre free of pain Ill write again but meantime go to ER and hopefully this time your problems will get sorted out. I have a suspicion that you're falling between the cracks in your care, it can happen when two or more doctors are involved.

Love Jan

:

Link to comment
Share on other sites

Guest guest

, I agree with Ginger, if your # are not going down something needs to be adjusted. The drugs we take are awful but they should work.

Patty

-----Original Message-----From: gehud119@... [mailto:gehud119@...] Sent: Wednesday, June 04, 2003 3:11 PM Subject: [ ] KARENHi, , I am surprized that the hep doc did not put you on imuran. I do not get my meds from rhemy, but from GI/hep. If your numbers are not going down, then something is wrong.Hugs, Ginger

Link to comment
Share on other sites

  • 2 weeks later...
Guest guest

Ginger,

The hep that I went to didn't do a thing other than confirm that I have AIH. He gave suggestions on meds and then basically passed the buck and said for me to see him in a year! I now have a new GI in Huntsville (the closest decent sized town - about 30 miles away). He is going to put me on Imuran when I see him on June 25th. He wanted to give my pancreas a chance to recover from the latest attacks. He also told me that I definitely have chronic pancreatitis and the episodes of severe RUQ abdominal pain, nausea, vomiting, and elevated liver enzymes are caused by my pancreas, not my liver. As you can imagine, this makes managing the AIH more complicated since the pancreatitis causes pretty major spikes in my liver enzymes. What we didn't know was that the spikes in my liver enzymes were most likely associated with a spike in one of the pancreas enzymes, lipase. The small hospital in my town doesn't bother to check the lipase since they can't do it in house. They only check the other pancreas enzyme, amylase. They would insist the pain couldn't be from the pancreas because my amylase was normal. I finally put the puzzle pieces together after a couple of visits to the hospital in Huntsville. They tested my lipase and the higher my liver enzymes, the higher the lipase. According to my internal med doc and my new GI, it is very common to have a normal amylase, but elevated lipase with pancreatitis. They said my lipase should have been checked every time I had an episode of pain, nausea, and vomiting. My labs last week revealed a normal AST and an ALT in the 90s - much improved from an AST of almost 800 and an ALT of about 500!

As you can see, I don't make things easy for my doctors as it seems I never present with a typical picture! The GI that was on call for my GI and saw me in the hospital over the weekend said that I 'certainly am a complicated and interesting case'. Don't know if she was talking about from a medical or psychiatric standpoint!

Thanks to all for the prayers and kind e-mails. I was going to try to thank each one personally but I just keep getting further behind on my e-mails.

W

Link to comment
Share on other sites

  • 3 months later...
  • 2 weeks later...

thanks Tina!

So, I got there at noon and the doc told me I could have been drinking as

much water as I wanted and could eat right after the first test (around 1).

I was so peeved b/c I actually called and expressed concern to the secretary

saying that I was breastfeeding and didn't want to go without water and she

told me that she e mailed the doc who told her that I could have 1 glass in

the early morning. So, needless to say, I'm pissed. It's not only the

world of endocrinology that has incompetent people. Anyway, without getting

into too much details, I'm pretty sure I have a medical malpractice suit

against the hosp. that delivered my baby a year ago. Believe me, I'm not a

sue-happy person AT ALL, but what has occurred is absolutely rediculous and

then to boot, THREE of their doctors misdiagnosed what they should have not

missed in the first place. Anyway, thanks for asking! It was great to see

you write your daughter's name the other day. We've heard so much about her

and never knew her name :)

----Original Message Follows----

From: " tina83862 " <tina8386@...>

Reply-hypothyroidism

hypothyroidism

Subject: Re: karen

Date: Thu, 02 Oct 2003 17:34:30 -0000

--how did you tests go the other day?? how is everything--been

waiting to hear back from your visit---tina

_________________________________________________________________

Instant message during games with MSN Messenger 6.0. Download it now FREE!

http://msnmessenger-download.com

Link to comment
Share on other sites

this always makes me crazy since I used to run a large doctor's office

(before kids)---why don't the girls at the desk --get up to ask the

doctor--ugggggg---anyway I am sorry you were told the wrong info--gee

this reminds me of when my dad had surgery and the hospital lost his

test results for surgery, they made him go from Sat. midnight till

Wed. noon time--He had colon cancer---anyway I flew into town and

gave him those complete liquid meals--told him he would never make it

into surgery because of the dehydration--we were right and he

survived the surgery after I yelled at the doctor for almost killing

my dad!!!!! It's amazing what total idiots they can be--one did not

tell the other and so forth--my dad dropped over 10 pounds from no

water or food in that time frame--imagine before surgery!!!!!! Talk

about a lawsuit!!!And this was after chemo--we did chemo first to

kill the cancer--it all worked out great and he is totally

recovered!!!

Opps I got off track--let us know what tests results you get--take

care tina

> thanks Tina!

> So, I got there at noon and the doc told me I could have been

drinking as

> much water as I wanted and could eat right after the first test

(around 1).

> I was so peeved b/c I actually called and expressed concern to the

secretary

> saying that I was breastfeeding and didn't want to go without water

and she

> told me that she e mailed the doc who told her that I could have 1

glass in

> the early morning. So, needless to say, I'm pissed. It's not only

the

> world of endocrinology that has incompetent people. Anyway,

without getting

> into too much details, I'm pretty sure I have a medical malpractice

suit

> against the hosp. that delivered my baby a year ago. Believe me,

I'm not a

> sue-happy person AT ALL, but what has occurred is absolutely

rediculous and

> then to boot, THREE of their doctors misdiagnosed what they should

have not

> missed in the first place. Anyway, thanks for asking! It was

great to see

> you write your daughter's name the other day. We've heard so much

about her

> and never knew her name :)

>

>

>

>

> ----Original Message Follows----

> From: " tina83862 " <tina8386@a...>

> Reply-hypothyroidism

> hypothyroidism

> Subject: Re: karen

> Date: Thu, 02 Oct 2003 17:34:30 -0000

>

> --how did you tests go the other day?? how is everything--been

> waiting to hear back from your visit---tina

>

> _________________________________________________________________

> Instant message during games with MSN Messenger 6.0. Download it

now FREE!

> http://msnmessenger-download.com

Link to comment
Share on other sites

  • 2 months later...

that's an interesting spin on things - thanks :)

----Original Message Follows----

From: Aprilcupcake@...

Reply-hypothyroidism

hypothyroidism

Subject: karen

Date: Mon, 8 Dec 2003 08:26:44 EST

I was talking with my doc on friday about the reluctance of many

physicians to prescribe medication according to symptoms and not

numbers. She tells me it is most likely that they are in fear of

legal action should something go wrong.

And therefore they tend to " play by the rules " .

She wondered if they could perhaps have their patients sign

something like a release form that would limit their

liability if the patient wanted to increase their meds on their own.

Something to think about?

Chriss.

Link to comment
Share on other sites

My doctor was really against giving me Armour. He said no one else prescribed

it, and other doctors would think he was crazy. That DOES have something to do

with fear of lawsuits, since many medical boards and quality assurance boards

use " peer review. " Peer review means the person's actions are reviewed by a

group of people in the same profession. If you're asking for something many

doctors are against, it makes sense that your doctor would not be very compliant

with your requests. I did get my doctor to give me Armour, though. I brought

some medical journal articles on T3 and was arguing for Thyrolar (which he was

REALLY against--he said it was only used for thyroid cancer and any other doctor

would think he was absolutely crazy to prescribe it). I finally said, " Look.

I'm in an HMO. I CAN'T sue you, even if I were willing to. And, you're

agreeing to try me on something *I* am asking for. You really can't lose here. "

He agreed to the Armour, but I had to agree to call

him once a week to check in on progress.

K a r e n P <karlynn17@...> wrote:that's an interesting spin on things -

thanks :)

----Original Message Follows----

From: Aprilcupcake@...

Reply-hypothyroidism

hypothyroidism

Subject: karen

Date: Mon, 8 Dec 2003 08:26:44 EST

I was talking with my doc on friday about the reluctance of many

physicians to prescribe medication according to symptoms and not

numbers. She tells me it is most likely that they are in fear of

legal action should something go wrong.

And therefore they tend to " play by the rules " .

She wondered if they could perhaps have their patients sign

something like a release form that would limit their

liability if the patient wanted to increase their meds on their own.

Something to think about?

Chriss.

Link to comment
Share on other sites

do you feel better on Armour?

----Original Message Follows----

From: <melmac2525@...>

Reply-hypothyroidism

hypothyroidism

Subject: RE: karen

Date: Mon, 8 Dec 2003 08:41:52 -0800 (PST)

My doctor was really against giving me Armour. He said no one else

prescribed it, and other doctors would think he was crazy. That DOES have

something to do with fear of lawsuits, since many medical boards and quality

assurance boards use " peer review. " Peer review means the person's actions

are reviewed by a group of people in the same profession. If you're asking

for something many doctors are against, it makes sense that your doctor

would not be very compliant with your requests. I did get my doctor to give

me Armour, though. I brought some medical journal articles on T3 and was

arguing for Thyrolar (which he was REALLY against--he said it was only used

for thyroid cancer and any other doctor would think he was absolutely crazy

to prescribe it). I finally said, " Look. I'm in an HMO. I CAN'T sue you,

even if I were willing to. And, you're agreeing to try me on something *I*

am asking for. You really can't lose here. " He agreed to the Armour, but I

had to agree to call

him once a week to check in on progress.

_________________________________________________________________

Don’t worry if your Inbox will max out while you are enjoying the holidays.

Get MSN Extra Storage! http://join.msn.com/?PAGE=features/es

Link to comment
Share on other sites

Your Dr. is an idiot,...I take Thyrolar and actually prefer it

over Armour.It is basically the same thing except for it doesn't contain

the other T's.I feel absolutely wonderful on it.Find another dr.!!..My

mother treid the same thing with her Dr. and she was also told no for

Thyrolar because her dr. told her is was a drug for depression,not

thyroid...HELLO??...look at the name???....hehehe

Deneen:):)

Link to comment
Share on other sites

Well, he did give me the Armour, but he was a bit of an idiot. I am going to

visit one of the doctors from Shomon's Top Docs list in January. I will

be off of my HMO and will be able to choose my own doctor. I think if you have

something like Hashimoto's that requires a lot of understanding and lots of

tinkering with medicine, an HMO is not the best route...at least not for me.

jezebel56@... wrote:Your Dr. is an idiot,...I take Thyrolar and

actually prefer it

over Armour.It is basically the same thing except for it doesn't contain

the other T's.I feel absolutely wonderful on it.Find another dr.!!..My

mother treid the same thing with her Dr. and she was also told no for

Thyrolar because her dr. told her is was a drug for depression,not

thyroid...HELLO??...look at the name???....hehehe

Deneen:):)

Link to comment
Share on other sites

Ginger,

You already have done something to help - your prayers mean the world to me. They must be working because I am feeling close to human again!

thanks to everyone for all the prayers and kind words. you guys are the greatest!

W

Link to comment
Share on other sites

  • 9 months later...

I think u need a new biopsy with a hospital you trust. I was told to always go to the same place because different people read slides different ways. I hope you get some answers and feel better soon. We know the liver can heal it self but since they are all looking at the same slide it is very confusing. Being tired could be from yur liver or all th panc. attacks you've had you need someone to do a full work up and get to the bottom of this.

Good luck

the WV hillbilly

Link to comment
Share on other sites

I agree in getting the biopsy re-done, but what a pain. One is bad

enough. Whatever clinic U are going to doctor with, have it done

there. The Mayo Clinic and Dr Czar(?) is what Kels specialists follow

as her treatment.

Trish

> I think u need a new biopsy with a hospital you trust. I was

told to

> always go to the same place because different people read slides

different ways.

> I hope you get some answers and feel better soon. We know the liver

can heal

> it self but since they are all looking at the same slide it is very

confusing.

> Being tired could be from yur liver or all th panc. attacks you've

had you

> need someone to do a full work up and get to the bottom of this.

> Good luck

> the WV hillbilly

Link to comment
Share on other sites

  • 1 month later...

: So it ok to give more than 1 PEP & ZP at a meal. I only give one per

meal and not any in between. My son usually only snacks in school. By the

time he gets home it is dinner time. His largest meal is dinner. He has

been on the enzymes building up for the past month. Seeing some small

improvements but not too much. What do you think? EIleen

>From: " jornmatt " <kjorn@...>

>Reply-

>

>Subject: Re: new on enzymes and have questions

>Date: Sat, 27 Nov 2004 22:05:06 -0000

>

>

>>

>The Complete isn't as effective for most people so a higher dose

>(like 3-4 capsules per meal instead of the 1-2 most people discuss

>here with HNI) might give you the improvements again.

>

>.

>

>

>

>

Link to comment
Share on other sites

  • 1 month later...

FIGURES!!!!!!!!!!!!!!!!!!!!!!

>From: " jornmatt " <kjorn@...>

>Reply-

>

>Subject: ***Re: mature moms/ header

>Date: Sat, 15 Jan 2005 19:57:36 -0000

>

>

>As interesting as this is, you might want to continue this thread

>with a different header....it is being picked up and flagged by some

>spam watching software utilities (as adult content).

>

>.

><smiling widely>

>

>

>

>

>

Link to comment
Share on other sites

  • 7 months later...

Hello! I'm so sorry that you are having such a time of it! I do hope

that you might call the doc's office and see if you might be able to

arrange someone to at least get a wheel chair for you to be able to

get up the ramp to recovery! I know what you mean when it comes to a

chain of events that just never seems to end! Hopefully for your sake

it will soon!!! I just want to let you know that you are in my

thoughts and prayers!!! Take care and God Bless!!! XXX's Kim

Link to comment
Share on other sites

  • 2 months later...

,

Since my daughter is constipated, would it help her to take magnesium oxide?

Thanks,

Re: karen/ andrea

>>She was taking a magnesium oxide and I think that causes loose stools

so we need to maybe try a different mag.

Mag oxide is cheap and common is supplement but it is not absorbed

well. It promotes the laxative effect more that other forms. just about

any other form is better.

Supernuthera can cause hyperactivity and sleep problems. Phenols can

too, so your plan sounds wise. After take out the supernuthera and add

No-Fenol, you'll know more then. It would be great if you could post on

if these steps help or not. It is kind of a process getting everything

taken care of.

.

Link to comment
Share on other sites

  • 7 months later...
Guest guest

Hi - I finally was diagnosed a couple of years ago with lyme and

babesia..... buhner's book on lyme is really very good and tells you more

than you would ever want to know about the herbs he uses...

Before I had the lyme/babs diagnosis, my attittude was to try anything and

everything in the hopes something would work!!! and occasionally things did

work - but only for awhile......but antibiotics have alwats helped....

Good luck,

Deb

Link to comment
Share on other sites

Guest guest

Hi Deb. " Healing Lyme " is the book? I googled his name and " lyme "

and that's what came up first.

Yes, boy, to I know about the virtues of antibiotics! Whew...yes,

knock wood. But I'm a little limited in what I can do right now.

Major life adjustments going on, big-time, so I'm trying to start

with " small " and " natural. " I'm thinking I will probably get to

being tested for Lyme, too, eventually, as there's that possibility

in my history too. It certainly gets to be a big mess, trying to

figure out where all the " this " came from.

Thank you for the help, Deb. I can see there's even more reading on

my horizon!

:)

>

>

>

>

> Hi - I finally was diagnosed a couple of years ago with lyme

and babesia..... buhner's book on lyme is really very good and

tells you more than you would ever want to know about the herbs he

uses...

>

> Before I had the lyme/babs diagnosis, my attittude was to try

anything and everything in the hopes something would work!!! and

occasionally things did work - but only for awhile......but

antibiotics have alwats helped....

>

> Good luck,

> Deb

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...