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TESS:

It seems to me they should be giving you something to counter-act the allergy

not fishing around to find an anti-biotic that works for you until the problem

of the allergy is solved. The Benedryl did to me what you are describing and as

I said they had to go to atarax. Please see someone before it gets to the stage

where you end up in the ER as I was fighting to breath because the throat was

nearly swollen shut and my itchies had gone to a swollen face and also the

inside of my mouth.

I care Tess and want you to get help...

Love and many prayers.

Jan (((hugs)))

tess_northwest@... wrote:

Hi...the itching/welting subsided during the night. I started on the

keflex today, and after two doses have the stupid itching and welting

all over again. So I'm off the keflex. Now they're trying me on

clindamycin. I've been on benedryl but it hasn't helped. This is getting

me down...the itching is driving me bananas and makes me want to throw

plates or something - which I won't. My legs & back are bumpy with welts

of various length and size. There is itching between my fingers, scalp,

everywhere. I have my inhaler handy, and told my daughter if anything

more wacky happens and I can't tell her not to, then call 911. I am

probably over-reacting but this awful itching is so bad. Hopefully when

the keflex gets out of my system it will stop as clindamycin is a

different type of antibiotic. Prayers & hugs needed.

Love...

Tess

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Tess

Have you tried a milk bath or oatmeal bath? Just sprinkle about a cup

of powdered milk in the running water then soak. You can do this with

oatmeal too. About 1/2 cup to start, I don't know how big your tub is,

but you need to put it in a processor to get it ground up really fine.

A lot cheaper than those name brand soaks.

-----Original Message-----

From: tess_northwest@... [mailto:tess_northwest@...]

Hi...the itching/welting subsided during the night. I started on the

keflex today, and after two doses have the stupid itching and welting

all over again. So I'm off the keflex. Now they're trying me on

clindamycin. I've been on benedryl but it hasn't helped. This is getting

me down...the itching is driving me bananas and makes me want to throw

plates or something - which I won't. My legs & back are bumpy with welts

of various length and size. There is itching between my fingers, scalp,

everywhere. I have my inhaler handy, and told my daughter if anything

more wacky happens and I can't tell her not to, then call 911. I am

probably over-reacting but this awful itching is so bad. Hopefully when

the keflex gets out of my system it will stop as clindamycin is a

different type of antibiotic. Prayers & hugs needed.

Love...

Tess

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Geez, Tess, you don't need that!

Wish I could give you some magic suggestion that would clear it all

up in a jiffy. Maybe drinking lots of water to flush the other stuff

out of your system? I hope it clears up soon. Keep a watch that

your lips, tongue, and mouth don't swell.

Love ya,

Judi

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You must be so uncomfortable, Tess. That's really awful.

Don't take any chances. I'm glad Em is there to keep an eye on you.

Please keep us posted.

[ ] feeling bad

> Hi...the itching/welting subsided during the night. I started on the

> keflex today, and after two doses have the stupid itching and welting

> all over again. So I'm off the keflex. Now they're trying me on

> clindamycin. I've been on benedryl but it hasn't helped. This is

getting

> me down...the itching is driving me bananas and makes me want to throw

> plates or something - which I won't. My legs & back are bumpy with

welts

> of various length and size. There is itching between my fingers,

scalp,

> everywhere. I have my inhaler handy, and told my daughter if anything

> more wacky happens and I can't tell her not to, then call 911. I am

> probably over-reacting but this awful itching is so bad. Hopefully

when

> the keflex gets out of my system it will stop as clindamycin is a

> different type of antibiotic. Prayers & hugs needed.

>

> Love...

>

> Tess

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HiTess,

hope/you/fee/better/soon...hug,

joy

[ ] feeling bad

Hi...the itching/welting subsided during the night. I started on the

keflex today, and after two doses have the stupid itching and welting

all over again. So I'm off the keflex. Now they're trying me on

clindamycin. I've been on benedryl but it hasn't helped. This is getting

me down...the itching is driving me bananas and makes me want to throw

plates or something - which I won't. My legs & back are bumpy with welts

of various length and size. There is itching between my fingers, scalp,

everywhere. I have my inhaler handy, and told my daughter if anything

more wacky happens and I can't tell her not to, then call 911. I am

probably over-reacting but this awful itching is so bad. Hopefully when

the keflex gets out of my system it will stop as clindamycin is a

different type of antibiotic. Prayers & hugs needed.

Love...

Tess

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Aw Tess!! You need way more than hugs and prayers. I am sending

you my guardian angel. You need it. Please send her back when you

are better, and know that you are in my prayers.

> Hi...the itching/welting subsided during the night. I started on

the

> keflex today, and after two doses have the stupid itching and

welting

> all over again. So I'm off the keflex. Now they're trying me on

> clindamycin. I've been on benedryl but it hasn't helped. This is

getting

> me down...the itching is driving me bananas and makes me want to

throw

> plates or something - which I won't. My legs & back are bumpy with

welts

> of various length and size. There is itching between my fingers,

scalp,

> everywhere. I have my inhaler handy, and told my daughter if

anything

> more wacky happens and I can't tell her not to, then call 911. I am

> probably over-reacting but this awful itching is so bad.

Hopefully when

> the keflex gets out of my system it will stop as clindamycin is a

> different type of antibiotic. Prayers & hugs needed.

>

> Love...

>

> Tess

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  • 2 years later...

I don't want to sound discouraging to anyone, but I am feeling worse

than ever. My chest pain is so bad that I can hardly move my arms, and

it doesn't help to lie down, it hurts so bad to get there and then,

once I am lying down, I wince in pain to even slightly move my head or

arms. I feel really selfish for complaining to you all, when you have

all been though this and so much more. But I know you all understand

and I am really having a pity party right now - tears and all. I just

can't wait to get well and be able to go to all the doctors who told me

that it wasn't the implants that were causing my pain, and say SEE, it

was the implants!! Am I even making any sense? Thanks for listening.

Cherie

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Hi Cherie - I feel for you and I totally understand your sadness.

It doesn't seem like this is the kind of illness that goes away

overnight, and for some people it takes a few years for their bodies

to bounce back. I also remember reading that sometimes the symptoms

get worse after surgery, and then slowly start to improve. My body

was already ravaged by the implants when I had the explants, so it

wasn't at it's optimum condition. I'm definitely still having

symptoms, and even though I would have loved to feel normal again

right away, it seems to take longer. Some days are better than

others - yesterday I had alot of fatigue, but today was a good day.

The first week after the surgery, my heart was beating quite heavy,

and I'd wake up in the night because my body was twitching. Anyway,

what I'm trying to say is that you are not alone - and please any

time you're feeling depressed about the pain you're in, continue to

reach out to us. You are not being selfish by any means, you have

been through alot and you're fighting to get your health back. You

are so brave for making the decision to get the implants removed,

and I know sometimes I think " geez, what if it's really NOT the

implants? " , but you know what, I never would have felt sane if I

kept them in my body. I believe in time we will get the validation

we are looking for, so be kind to yourself. I feel they would have

continued to wreak havoc on my body, and then I would have never had

a chance.

Sis

--- In , " Cherie " <cheriesut@y...>

wrote:

>

> I don't want to sound discouraging to anyone, but I am feeling

worse

> than ever. My chest pain is so bad that I can hardly move my

arms, and

> it doesn't help to lie down, it hurts so bad to get there and

then,

> once I am lying down, I wince in pain to even slightly move my

head or

> arms. I feel really selfish for complaining to you all, when you

have

> all been though this and so much more. But I know you all

understand

> and I am really having a pity party right now - tears and all. I

just

> can't wait to get well and be able to go to all the doctors who

told me

> that it wasn't the implants that were causing my pain, and say

SEE, it

> was the implants!! Am I even making any sense? Thanks for

listening.

> Cherie

>

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Cherie,

What have you been doing - or not doing? . . .

If you are still working on detox programs, you need

to back off completely until you're feeling better.

Some people, like Kathie, have some very bad herxes! .

.. . She had to go very, very slowly. Nevertheless,

she's made outstanding progress.

I'd suggest using ice packs on your chest if you

suspect the pain is caused by swelling.

Are you taking anything for pain? . . . If not, can

you take Ibprophen? . . . or something like Tylenol or

Motrin?

I feel so bad for you having so much pain. This is not

the way it goes for most women. . . I'm sure they'll

confirm that. There may be rocky days, but I can't

remember anyone describing the kind of pain you're

talking about!

Be sure to drink plenty of water. . . At least 1/2

ounce per pound of body weight each day.

I can't remember. . . Who was your doctor?

Please keep hanging in there . . This too shall pass!

We're here if you need us!

Hugs and prayers,

Rogene

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Cherie

I hope you get to feeling better soon. It really is miserable

living in pain. Hopefully things are looking up. Your chest pain

may have been aggravated by the surgery. I have had fms for twenty

years and I have in the past gotten my chest so sore from coughing

that they actually did an mri thinking I had done something to a

rib. When they couldn't find anything, they decided that I must

have pleurisy. I remember my pain being so bad that I was in tears

trying to raise my arm. Well, I knew it wasn't pleurisy--it was

from the fibromyalgia. Another time I had a back xray because I was

in such pain they thought maybe it was a disc or something---nothing

showed. It was my fms. The reason I am telling you this is that

fms can produce extremely severe pain at times that can be mistaken

for just about anything. I have had chest pain all over my chest in

my chest wall--especially between my breasts and to the side of both

breasts and under them. This was very persistent. Before explant,

I used to push really hard between my breasts so I could take a

breath that felt full. Apparently the muscles were binding up that

area and not allowing my lungs to take a good breath. Since explant

and alot of detoxing I rarely get any of those pains anymore. But

when I start herxing alot, the chest pain ---especially under my

left breast--comes back. I am not sure why. I also had severe neck

pain before explant. That has slowly gotten alot better. So hang

in there. I do believe whatever the cause of your pain, it will

definitely improve over time. TAke care.

Hugs, kathy

--- In , " Cherie " <cheriesut@y...>

wrote:

>

> Rogene

> I may be detoxing too much - my natural doc has me on many

> supplements to help me detox. Also I am taking epsom salt baths

> because right after I take them I feel better. I have been

drinking

> green tea and juicing organic fruits and vegies twice a day. I

> drink about three bottled waters a day. I am having a hard time

> giving up sugar though. I'm not sure if I am sick with some sort

of

> virus, or maybe it's herxing. I'm sensitive to all over-the-

counter

> pain meds, and only have hydrocodone. I had been off the

> hydrocodone for the last month since the surgery, but last night

and

> this morning I was in so much discomfort that I took it. I also

> take Benadryl every day for my allergies, which I know I should

stop

> soon. But without it I sneeze and itch all over. I know the

> prednisone would be bad to take, but it's so hard, because I know

a

> steroid taper would get rid of my pain - for now anyway. I should

> probably throw them away, because they are a temptation.

>

> My doc was the surgeon who put the implants in. It was a good

> experience, and he agreed it was best to have them out. He

assured

> me that he removed the capsules, and I don't think he would lie to

> me. I do have a little doubt in my mind only because the

procedure

> only took an hour.

>

> I really do appreciate the support. My husband just feels so bad

> for me - that the pain never really goes away. I just keep

telling

> myself that this is not all for nothing. My relationship with

> Christ has grown so much, and I know that He works out all things

> for the good for those who love him. I guess I just really wanted

> to get well immediately after the implants came out so that I

would

> have no doubt that they were what was making me sick.

>

> When others say they have chest pain, do you know if they mean

high

> in the chest, or in the breast area? Mine is high, from the

middle -

> my sternum and out both clavicles and up into the neck.

> Rheumatologist and radiology said spondyloarthropathy (form of

> arthritis).

> Hugs back,

> Cherie

>

> --- In , Rogene S <saxony01@y...>

wrote:

> >

> > Cherie,

> >

> > What have you been doing - or not doing? . . .

> >

> > If you are still working on detox programs, you need

> > to back off completely until you're feeling better.

> > Some people, like Kathie, have some very bad herxes! .

> > . . She had to go very, very slowly. Nevertheless,

> > she's made outstanding progress.

> >

> > I'd suggest using ice packs on your chest if you

> > suspect the pain is caused by swelling.

> >

> > Are you taking anything for pain? . . . If not, can

> > you take Ibprophen? . . . or something like Tylenol or

> > Motrin?

> >

> > I feel so bad for you having so much pain. This is not

> > the way it goes for most women. . . I'm sure they'll

> > confirm that. There may be rocky days, but I can't

> > remember anyone describing the kind of pain you're

> > talking about!

> >

> > Be sure to drink plenty of water. . . At least 1/2

> > ounce per pound of body weight each day.

> >

> > I can't remember. . . Who was your doctor?

> >

> > Please keep hanging in there . . This too shall pass!

> > We're here if you need us!

> >

> > Hugs and prayers,

> >

> > Rogene

> >

>

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Cherie,

Check to see if any of the medications (including

OTC's) you're taking contain any form of silicone

dioxide . . . One of our SiliconeKids mothers, and her

children, did much better after removing as many

silicone related materials from their environment as

possible. One of her children experienced a severe

case of poisoning from an over-the-counter medication

containing silicone dioxide.

Over time their sensitivity has decreased

considerably.

Hugs,

Rogene

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Rogene

I checked into Tylenol and Motrin, both of which I haven't been able

to take in so long, and they both have silicon dioxide. I can't

believe it! I could actually be sensitive to that, and not allergic

to the actual active ingredient. Do you know any other chemical

names to look for, or what other types of products of everyday

living that might contain it? This is just a real revelation to me,

and I can't wait to learn more - thank you so much.

Cherie

>

>

> Cherie,

>

> Check to see if any of the medications (including

> OTC's) you're taking contain any form of silicone

> dioxide . . . One of our SiliconeKids mothers, and her

> children, did much better after removing as many

> silicone related materials from their environment as

> possible. One of her children experienced a severe

> case of poisoning from an over-the-counter medication

> containing silicone dioxide.

>

> Over time their sensitivity has decreased

> considerably.

>

> Hugs,

>

> Rogene

>

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Cherie,

There are many, many preparations that have silicone

dioxide. . . You'll need to check the labels on

everything if you suspect you're reacting to it.

Why? I don't know. I'd suggest contacting Lana

<lanadearest@...>. She left no stone unturned

to find out where all the silicone dioxide was hidden

so she could help her kids. Her sons went from being

chronically ill, to doing very well after she stopped

their silica exposure.

Hugs,

Rogene

--- Cherie <cheriesut@...> wrote:

> Rogene

> I checked into Tylenol and Motrin, both of which I

> haven't been able

> to take in so long, and they both have silicon

> dioxide. I can't

> believe it! I could actually be sensitive to that,

> and not allergic

> to the actual active ingredient. Do you know any

> other chemical

> names to look for, or what other types of products

> of everyday

> living that might contain it? This is just a real

> revelation to me,

> and I can't wait to learn more - thank you so much.

> Cherie

>

> >

> >

> > Cherie,

> >

> > Check to see if any of the medications (including

> > OTC's) you're taking contain any form of silicone

> > dioxide . . . One of our SiliconeKids mothers, and

> her

> > children, did much better after removing as many

> > silicone related materials from their environment

> as

> > possible. One of her children experienced a severe

> > case of poisoning from an over-the-counter

> medication

> > containing silicone dioxide.

> >

> > Over time their sensitivity has decreased

> > considerably.

> >

> > Hugs,

> >

> > Rogene

> >

>

>

>

>

>

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  • 2 years later...
Guest guest

Ask your doc if you can try Armour. Http://www.stopthethyroidmadness.com

cw

-- feeling bad

Sometimes i feel my thyroid symptoms seem to reappear before and during my

cycle. Is it possible? What do I do when i get like this? My doctor has me

on effexors. 150mg. I have been on them since I discovered I had thyroid

disease. 5 years. And when i am PMSing, I have to take double. Because my

anxiety and depression seems to get worst. I feel tired achy just miserable.

Chuck B <gumboyaya@...> wrote: sweetwulfie wrote:

>

> Gatorade is not a good idea, it has Brominated vegetable oil in it.

Not all flavors have bromine. Only the Orange and X-factor have it.

I still wouldn't drink it because of all the sugar.

Chuck

---------------------------------

You rock. That's why Blockbuster's offering you one month of Blockbuster

Total Access, No Cost.

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Guest guest

Jane wrote:

>

>

> Sometimes i feel my thyroid symptoms seem to reappear before and during

> my cycle. Is it possible?...

Certainly. Sex and thyroid hormones have similar binding proteins, which

could affect each other. I believe there are other interactions as well,

which I haven't paid much attention to, given my lack of such cycles. If

nothing else, retaining water will increase the dosage needed for all

your prescriptions.

Chuck

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