Jump to content
RemedySpot.com
Sign in to follow this  
Guest guest

New Member

Rate this topic

Recommended Posts

Guest guest

> Amiodarone and interferon- have been reported to induce a wide > variety of functional disorders of the thyroid; discussion is beyond > the scope of this review. However, both drugs can induce thyroiditis > with hyperthyroidism, and patients receiving these drugs should be > closely monitored.> I gave my regular physician a copy of Avonex's warnings and cautions paper. I told him that I thought that I might be having problems from that. However, the neurologist (butthead that he is) refuses to believe that any type of interferon would do that. >> > Do you have your lab results? No I don't but I am looking into getting them.> With a cyst it is possible for it to what is called a hot nodule and > be the cause of the hyper symptoms or it could be your medication or > the Cyst could ( less than 5 % chance) be the big C and requires > further investigation as to why you are hyper. Doctor just wants to "monitor" it. I don't know what to watch for except more heart problems. I also had a holter monitor put on and all that found was one skipped heartbeat. I thought it was odd considering it was pounding and jumping throughout the twenty fours I had it on. I thought about getting a second opinion. I am just sick of being sick and tired of being tired and really don't care for seeing more doctors. The MS causes my face on the one side to hurt but I wasn't really sure about the numbness. I have so many things wrong and I don't know what to do anymore. I feel like a hypochondriac but really I don't think I am. I think... lol Liz> > Kats3boys>

Share this post


Link to post
Share on other sites
Guest guest

Being hyper can cause the twitching.. I had that when I was in storm..... I don't agree with your docs not doing anything... being hyper is not a good thing, especially if your weight is dropping on it's own.....

Can you post your last labs for us to see? I'd like to see with they tested for the thyroid stuff..... I'd like to see what is causing you to be hyper....

I'm thinking it's not going to be much fun being hyper with MS.....

Topper ()

On Mon, 07 Nov 2005 14:07:19 -0000 "lizzydizzybutt" writes:

Hello, my name is . I have been diagnosed with hyperthyroidism a couple of months ago. I was having heart palpitations and was losing weight without even trying. I had several tests done and they found a cyst on my thyroid. Doctor didn't want to put me on any medication or do any treatments unless the thyroid causes me problems with breathing. I have been having weird problems since then. I also have Multiple Sclerosis. So I don't know what is going on, to be truthful. My right eye has been spazzing like a twitch but within the eye itself. I know it isn't the eye lid. Now my face is numb on the left side. Anyone have this problem? Thanks for any help.

Share this post


Link to post
Share on other sites
Guest guest

Welcome!!! I'm glad you are getting well. My little guy is the Celiac

, so far. The other children will be tested next month. My husband

and I are not Celiacs, however, if our children are, dh has a shock

waiting for him b/c if the majority of members in the house are GF,

then we all are going to be. Of coure, after I read Dangerous Grains,

we might all be anyway -- I requested the library to buy a copy and

they did! It is here and I'm going to go check it out tomorrow!!!

I thought you were supposed to be on a high gluten diet when they do

the biopsy as the biospy is looking for damaged villi. I would call

and ask your GI to make sure, however, b/c an adult may not heal as

quickly as a child given the years of damage, it may not matter with

only going GF for a few weeks.

Our son is not getting the biospy done, b/c we will not put him on a

high gluten diet, a diet he never ate to begin with. He naturally

choose a more Paleo diet from the first solid food introduction time

frame. He's also only 3 1/2 yrs old and isn't able to understand, I'm

eating no wheat, now they want me to eat what they told me I

couldn't... Plus potty training issues, mistaken ingestion of gluten

cause a change in clothes, not very good for a child's development and

self-esteem.

His dx was made on positive IGG, DQ2 and positive GF diet experience.

The pediatrician is happy with that 'for now'. The Pedi GI doctor is

pushing for the biopsy and just doesn't seem to get we don't care, we

have a well child now and he is growing and happy...

I measured him today, he has grown almost an entire inch since Nov

26th, that's 38 days!!!

Maybe you got sick and had to cancel the biopsy for a reason unknown

to us here on earth. I believe in fate and God's hand ruling over our

lives. The biopsy is the 'gold standard' for diagnosis, but not

everyone with CD goes and gets it done. Positive blood test all

around and positive reaction to the GF diet should be enough in most

cases.

I'm obviously not one for doing invasive procedures when they clearly

have no benefit. But that is just me...

Rejoyce

Winchester, VA

Share this post


Link to post
Share on other sites
Guest guest

Welcome!!! I'm glad you are getting well. My little guy is the Celiac

, so far. The other children will be tested next month. My husband

and I are not Celiacs, however, if our children are, dh has a shock

waiting for him b/c if the majority of members in the house are GF,

then we all are going to be. Of coure, after I read Dangerous Grains,

we might all be anyway -- I requested the library to buy a copy and

they did! It is here and I'm going to go check it out tomorrow!!!

I thought you were supposed to be on a high gluten diet when they do

the biopsy as the biospy is looking for damaged villi. I would call

and ask your GI to make sure, however, b/c an adult may not heal as

quickly as a child given the years of damage, it may not matter with

only going GF for a few weeks.

Our son is not getting the biospy done, b/c we will not put him on a

high gluten diet, a diet he never ate to begin with. He naturally

choose a more Paleo diet from the first solid food introduction time

frame. He's also only 3 1/2 yrs old and isn't able to understand, I'm

eating no wheat, now they want me to eat what they told me I

couldn't... Plus potty training issues, mistaken ingestion of gluten

cause a change in clothes, not very good for a child's development and

self-esteem.

His dx was made on positive IGG, DQ2 and positive GF diet experience.

The pediatrician is happy with that 'for now'. The Pedi GI doctor is

pushing for the biopsy and just doesn't seem to get we don't care, we

have a well child now and he is growing and happy...

I measured him today, he has grown almost an entire inch since Nov

26th, that's 38 days!!!

Maybe you got sick and had to cancel the biopsy for a reason unknown

to us here on earth. I believe in fate and God's hand ruling over our

lives. The biopsy is the 'gold standard' for diagnosis, but not

everyone with CD goes and gets it done. Positive blood test all

around and positive reaction to the GF diet should be enough in most

cases.

I'm obviously not one for doing invasive procedures when they clearly

have no benefit. But that is just me...

Rejoyce

Winchester, VA

Share this post


Link to post
Share on other sites
Guest guest

I myself do not have thyroid cancer but I can tell you that switching your diet

to natural and organic foods will help your body stay healthy as well as

drinking lots of water (purified or bottled if you can help it). Minerals that

are deemed safe in our tap water can interfere with thyroid medication

absorption (I know mine does).

I'm not sure if you can get proper dosing on synthetic hormones as many like

synthroid only have certain hormones where something natural like armour will

have many many more. You might want to ask your doc about that. Needless to

say you will probably be a bit hypo for the rest of your life unless your docs

are really good about listening to your body and your blood work.

Try to find as much education as you can and keep yourself focused on your

goals. Being diagnosed with something like cancer can send you quite a blow.

Good luck and keep us updated.

Quoting Elaine :

>

>

>

>

> Hi folks,

>

> I was diagnosed with Thyroid Cancer on Friday. 

>

> What is life like after Thyroid cancer?

>

>

>

> I will have surgery on Feb. 16th.  Any advice?

>

>

>

> I'm more concerned about what to expect after surgery? How I will feel

>

> after having my thyroids removed, how will the synthetic medications

>

> work?

>

>

>

> I've struggled with sore throats, chronic ear aches, infections,

>

> fatigue and more fatigue.  I'm hoping that after the surgery and the

>

> radiation treatment that I can be more energetic and stronger.  Has

>

> anyone have any success stories to share regarding Thyroid cancer. 

>

>

>

> Thanks,

>

> Elaine

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

Share this post


Link to post
Share on other sites
Guest guest

I myself do not have thyroid cancer but I can tell you that switching your diet

to natural and organic foods will help your body stay healthy as well as

drinking lots of water (purified or bottled if you can help it). Minerals that

are deemed safe in our tap water can interfere with thyroid medication

absorption (I know mine does).

I'm not sure if you can get proper dosing on synthetic hormones as many like

synthroid only have certain hormones where something natural like armour will

have many many more. You might want to ask your doc about that. Needless to

say you will probably be a bit hypo for the rest of your life unless your docs

are really good about listening to your body and your blood work.

Try to find as much education as you can and keep yourself focused on your

goals. Being diagnosed with something like cancer can send you quite a blow.

Good luck and keep us updated.

Quoting Elaine :

>

>

>

>

> Hi folks,

>

> I was diagnosed with Thyroid Cancer on Friday. 

>

> What is life like after Thyroid cancer?

>

>

>

> I will have surgery on Feb. 16th.  Any advice?

>

>

>

> I'm more concerned about what to expect after surgery? How I will feel

>

> after having my thyroids removed, how will the synthetic medications

>

> work?

>

>

>

> I've struggled with sore throats, chronic ear aches, infections,

>

> fatigue and more fatigue.  I'm hoping that after the surgery and the

>

> radiation treatment that I can be more energetic and stronger.  Has

>

> anyone have any success stories to share regarding Thyroid cancer. 

>

>

>

> Thanks,

>

> Elaine

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

>

Share this post


Link to post
Share on other sites
Guest guest

Just wanted to introduce myself as I read through a lot of previous posts.My name is Liz and I was recently diagnosed with a new primary tumor after a 12.5 year remission. I was diagnosed just after Thanksgiving and on Jan. 11 had a double mastectomy with double tram reconstruction. So far all is going well and am now awaiting a decision as to what kind of chemo follow-up I might need. I am not quite up to typing out my whole story, but I expect that will come eventually.I am in Michigan, so January is a good month to be stuck in the house while recuperating. -Liz

Share this post


Link to post
Share on other sites
Guest guest

Liz,

Sorry to hear about your reoccurance. I will keep you in my prayers.

Hugs

nne

Breast Cancer Patients Soul Mates for Lifehttp://www.geocities.com/chucky5741/breastcancerpatients.html

Check out my breast cancer ornaments at:http://www.geocities.com/chucky5741/bcornament.htmlalso check out my other ornaments and lots of nice gifts at:http://www.cancerclub.com

New Member

Just wanted to introduce myself as I read through a lot of previous posts.

My name is Liz and I was recently diagnosed with a new primary tumor after a 12.5 year remission. I was diagnosed just after Thanksgiving and on Jan. 11 had a double mastectomy with double tram reconstruction. So far all is going well and am now awaiting a decision as to what kind of chemo follow-up I might need. I am not quite up to typing out my whole story, but I expect that will come eventually.

I am in Michigan, so January is a good month to be stuck in the house while recuperating.

-Liz

Share this post


Link to post
Share on other sites
Guest guest

Liz,

I am new here to, but what a good group of people you have found. I read more than write, but there are some strong females pounding keys here.

Do you feel like Job? I had a near fatal car wreck in 2002, a major heart attack in 2002 and then breast cancer. I wanted to change my name for a while. The I decided it was my hand to play and I am doing my best to play it well. I know you will do the same thing.

And I have found it is easier to share the dark with those who have also been in it. Anytime you need to "talk" feel free.

Deborah

Deborah aka

Deborah Page

deborah_ann_page@...

"A woman is like a teabag; you don't know how strong she is until you put her in hot water."

Eleanor Roosevelt

New Member

Just wanted to introduce myself as I read through a lot of previous posts.

Share this post


Link to post
Share on other sites
Guest guest

Hi Liz. So sorry to hear your back in the mix. THAT SUCKS!!

Trisha

-- New Member

Just wanted to introduce myself as I read through a lot of previous posts.

My name is Liz and I was recently diagnosed with a new primary tumor after a 12.5 year remission. I was diagnosed just after Thanksgiving and on Jan. 11 had a double mastectomy with double tram reconstruction. So far all is going well and am now awaiting a decision as to what kind of chemo follow-up I might need. I am not quite up to typing out my whole story, but I expect that will come eventually.

I am in Michigan, so January is a good month to be stuck in the house while recuperating.

-Liz

Share this post


Link to post
Share on other sites
Guest guest

Deborah, I got my cancer in 2002 and lost my Mom also in 2002 and found my boyfriend in 2002...Guess it was a bad and good year for both of us... I am kind of a new person to the group also... I am from North Carolina but grew up in Delaware retired and moved in 2004... If you want to talk anytime i am catwoman5020002000@... Betsy (NC) Note: forwarded message attached.

Liz,

I am new here to, but what a good group of people you have found. I read more than write, but there are some strong females pounding keys here.

Do you feel like Job? I had a near fatal car wreck in 2002, a major heart attack in 2002 and then breast cancer. I wanted to change my name for a while. The I decided it was my hand to play and I am doing my best to play it well. I know you will do the same thing.

And I have found it is easier to share the dark with those who have also been in it. Anytime you need to "talk" feel free.

Deborah

Deborah aka

Deborah Page

deborah_ann_page@...

"A woman is like a teabag; you don't know how strong she is until you put her in hot water."

Eleanor Roosevelt

New Member

Just wanted to introduce myself as I read through a lot of previous posts.

Share this post


Link to post
Share on other sites
Guest guest

Hi Liz, What type of bc is it? Is it the same kind that you had 12 years ago and what was your treatment 12 years ago? Hope to hear from you soon. This is a great site and very inspiring for me. Sharonmslizart wrote: Just wanted to introduce myself as I read through a lot of previous posts. My name is Liz and I was recently diagnosed with a new primary tumor after a 12.5 year remission. I was diagnosed just after Thanksgiving and on Jan. 11 had a double mastectomy with double tram reconstruction. So far all is going well and am now awaiting a decision as to what kind of

chemo follow-up I might need. I am not quite up to typing out my whole story, but I expect that will come eventually. I am in Michigan, so January is a good month to be stuck in the house while recuperating. -Liz HAVE YOU BOOKED YOUR VALENTINES RESERVATION YET? WWW.DOUBLETREE.COM ROMANCE PACKAGE WITH CHAMPAGNE, BREAKFAST AND JACUZZI SUITE

Yahoo! Autos. Looking for a sweet ride? Get pricing, reviews, more on new and used cars.

Share this post


Link to post
Share on other sites
Guest guest

hi liz, im in michigan also, cheboygan..use to live in monroe....i don't post often but currently getting gemzar. diagnosed 11 and 1/2 yrs ago. i am now stage 4

your right about michigan in january

hugs from carol in michigan

Share this post


Link to post
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...
Sign in to follow this  

×
×
  • Create New...