Re: OT: Rifing for mold (was Hyperreaction to cold air)

[Guest guest]

There are a lot of Rife frequencies for both general and specific molds, yeasts

and funguses, as well as allergies. But I have not gotten rid of my mold

problems yet. I also take probiotics and occasionally anti-fungals, but it is

very well established in my body.

Khaya

> >

> > Hi Susie,

> >

> > Forgot to mention one thing.  I found out not too long ago that I have

severe allergy to mold.  that's why all the running nose/problems happens

w/cold air.  the mold allergy also severely weakens the immune system even more

than lyme and coinfections.   the weak immune system is why I think I got the

staph and why I think its so hard to be in the cold air and feeling so ill the

next days.  

> >

> > I never knew I had mold in my place.  I had/have no visible mold but now

that I am more informed about mold, I am able to find it.  For example, if you

have any carpet in your place, you will imho have mold since carpet is a magnet

for dust and dust is a magnet for mold.  It doesn't affect people who don't

have mold allergy or weakened immune system.  so people don't pay attention to

it.  but we've got lyme and mold allergy so it affects us greatly.   I have

been doing mold remediation the past few months.  and I am planning to do mold

allergy desensitization.  I can give you more info regarding that if you want.

> >

> > Blessings,

> > Roxanne

> >  

> >

> >

> > ________________________________

> > From: tim2buk <tim2buk@>

> > To: Lyme_and_Rife

> > Sent: Thursday, May 10, 2012 12:30 PM

> > Subject: OT: Hyperreaction to cold air

> >

> >

> >  

> > Hi all,

> >

> > Was wondering if anyone is experiencing an increase in symptoms (headaches,

post-nasal drip, fatigue)when you are in an air-conditioning draft or even

outside on a nice day, but with a cool breeze blowing. My situation is so bad

that I have to wear a hat even at 60 or 62 degrees, and I still get an increase

in symptoms. In the winter, I need to wear a hat & a hooded jacket but I still

have worsening symptoms still. It is one of my most severe problems because it

limits me to the point that I have become more home-bound because I don't want

to become sicker than I already am. We've had to stop going out to eat because

no matter where I sit, I am in a draft & I become so stressed out because I know

I am going to have big problems in the next few days. I know I have low thyroid

(Hashimoto's) but other people do too & don't have the severe reactions that I

do. Unfortunately, I have been on all thyroid meds there are & none helped me,

only made me feel

> > worse, so my doctor said not to take anything. My TSH is usually around 3

or 4 (it's supposed to be around 1 or so). I've had tons of cortisol saliva

tests & mostly came back ok except for elevated night time saliva. I feel that

my adrenals must be shot but don't know what else to try for them either. The

glandulars make me nervous. Rhodiola helped me at one time, but then it stopped

giving me energy. I don't know if it is a lyme thing or what. I just wanted to

know if there is anybody else that is having these problems & how you are

dealing with them. Thanks for any thoughts.

> >

> > Susie

> >

>

[Guest guest]

Khaya,

One of these days when I am on an off-week for lyme rifing, I might just try a

general mold freq (I'll look it up in the CAFL) to see what happens. How do you

know that you have not gotten rid of your mold problems yet? Do you also get

sick from being cold? It's a very complex issue for sure. What's hard is

trying to determine what problem takes priority & what has to be worked on

first. We all need some good luck.

Susie

> > >

> > > Hi Susie,

> > >

> > > Forgot to mention one thing.  I found out not too long ago that I have

severe allergy to mold.  that's why all the running nose/problems happens

w/cold air.  the mold allergy also severely weakens the immune system even more

than lyme and coinfections.   the weak immune system is why I think I got the

staph and why I think its so hard to be in the cold air and feeling so ill the

next days.  

> > >

> > > I never knew I had mold in my place.  I had/have no visible mold but now

that I am more informed about mold, I am able to find it.  For example, if you

have any carpet in your place, you will imho have mold since carpet is a magnet

for dust and dust is a magnet for mold.  It doesn't affect people who don't

have mold allergy or weakened immune system.  so people don't pay attention to

it.  but we've got lyme and mold allergy so it affects us greatly.   I have

been doing mold remediation the past few months.  and I am planning to do mold

allergy desensitization.  I can give you more info regarding that if you want.

> > >

> > > Blessings,

> > > Roxanne

> > >  

> > >

> > >

> > > ________________________________

> > > From: tim2buk <tim2buk@>

> > > To: Lyme_and_Rife

> > > Sent: Thursday, May 10, 2012 12:30 PM

> > > Subject: OT: Hyperreaction to cold air

> > >

> > >

> > >  

> > > Hi all,

> > >

> > > Was wondering if anyone is experiencing an increase in symptoms

(headaches, post-nasal drip, fatigue)when you are in an air-conditioning draft

or even outside on a nice day, but with a cool breeze blowing. My situation is

so bad that I have to wear a hat even at 60 or 62 degrees, and I still get an

increase in symptoms. In the winter, I need to wear a hat & a hooded jacket but

I still have worsening symptoms still. It is one of my most severe problems

because it limits me to the point that I have become more home-bound because I

don't want to become sicker than I already am. We've had to stop going out to

eat because no matter where I sit, I am in a draft & I become so stressed out

because I know I am going to have big problems in the next few days. I know I

have low thyroid (Hashimoto's) but other people do too & don't have the severe

reactions that I do. Unfortunately, I have been on all thyroid meds there are &

none helped me, only made me feel

> > > worse, so my doctor said not to take anything. My TSH is usually around

3 or 4 (it's supposed to be around 1 or so). I've had tons of cortisol saliva

tests & mostly came back ok except for elevated night time saliva. I feel that

my adrenals must be shot but don't know what else to try for them either. The

glandulars make me nervous. Rhodiola helped me at one time, but then it stopped

giving me energy. I don't know if it is a lyme thing or what. I just wanted to

know if there is anybody else that is having these problems & how you are

dealing with them. Thanks for any thoughts.

> > >

> > > Susie

> > >

> >

>

[Guest guest]

No Susie, I am lucky that I don't get sick from being cold, and I am not

cold-blooded since I started taking natural thyroid. I'm not sure I'm more

sensitive to environmental mold than most other people--except for my allergy to

leaf mold (and I try to stay inside on windy days in spring and fall). But I

know I still am infected by several funguses, at least in my digestive system,

sinuses and feet. I have made LD my main treatment priority, but I'm getting

tired of being so bloated, so I'm back on a low-carb diet, for starters ... and

still thinking about MMS ...

Khaya

> > > >

> > > > Hi Susie,

> > > >

> > > > Forgot to mention one thing.  I found out not too long ago that I have

severe allergy to mold.  that's why all the running nose/problems happens

w/cold air.  the mold allergy also severely weakens the immune system even more

than lyme and coinfections.   the weak immune system is why I think I got the

staph and why I think its so hard to be in the cold air and feeling so ill the

next days.  

> > > >

> > > > I never knew I had mold in my place.  I had/have no visible mold but

now that I am more informed about mold, I am able to find it.  For example, if

you have any carpet in your place, you will imho have mold since carpet is a

magnet for dust and dust is a magnet for mold.  It doesn't affect people who

don't have mold allergy or weakened immune system.  so people don't pay

attention to it.  but we've got lyme and mold allergy so it affects us greatly.

  I have been doing mold remediation the past few months.  and I am planning

to do mold allergy desensitization.  I can give you more info regarding that if

you want.

> > > >

> > > > Blessings,

> > > > Roxanne

> > > >  

> > > >

> > > >

> > > > ________________________________

> > > > From: tim2buk <tim2buk@>

> > > > To: Lyme_and_Rife

> > > > Sent: Thursday, May 10, 2012 12:30 PM

> > > > Subject: OT: Hyperreaction to cold air

> > > >

> > > >

> > > >  

> > > > Hi all,

> > > >

> > > > Was wondering if anyone is experiencing an increase in symptoms

(headaches, post-nasal drip, fatigue)when you are in an air-conditioning draft

or even outside on a nice day, but with a cool breeze blowing. My situation is

so bad that I have to wear a hat even at 60 or 62 degrees, and I still get an

increase in symptoms. In the winter, I need to wear a hat & a hooded jacket but

I still have worsening symptoms still. It is one of my most severe problems

because it limits me to the point that I have become more home-bound because I

don't want to become sicker than I already am. We've had to stop going out to

eat because no matter where I sit, I am in a draft & I become so stressed out

because I know I am going to have big problems in the next few days. I know I

have low thyroid (Hashimoto's) but other people do too & don't have the severe

reactions that I do. Unfortunately, I have been on all thyroid meds there are &

none helped me, only made me feel

> > > > worse, so my doctor said not to take anything. My TSH is usually

around 3 or 4 (it's supposed to be around 1 or so). I've had tons of cortisol

saliva tests & mostly came back ok except for elevated night time saliva. I

feel that my adrenals must be shot but don't know what else to try for them

either. The glandulars make me nervous. Rhodiola helped me at one time, but

then it stopped giving me energy. I don't know if it is a lyme thing or what.

I just wanted to know if there is anybody else that is having these problems &

how you are dealing with them. Thanks for any thoughts.

> > > >

> > > > Susie

> > > >

> > >

> >

>

[Guest guest]

Susie, I do quite a bit of salt & C, but not necessarily at the same time. My

dependence on C is one of the reasons I've been putting of MMS. My doctor is

not a fan of CS, but I do have a CS throat spray that I use when I get a sore

throat. And I rince my mouth with CS before getting any dental work. But my

doctor says not to swallow it. I think because of yeast.

Khaya

> > > > > >

> > > > > > Hi Susie,

> > > > > >

> > > > > > Forgot to mention one thing.  I found out not too long ago that I

have severe allergy to mold.  that's why all the running nose/problems happens

w/cold air.  the mold allergy also severely weakens the immune system even more

than lyme and coinfections.   the weak immune system is why I think I got the

staph and why I think its so hard to be in the cold air and feeling so ill the

next days.  

> > > > > >

> > > > > > I never knew I had mold in my place.  I had/have no visible mold

but now that I am more informed about mold, I am able to find it.  For example,

if you have any carpet in your place, you will imho have mold since carpet is a

magnet for dust and dust is a magnet for mold.  It doesn't affect people who

don't have mold allergy or weakened immune system.  so people don't pay

attention to it.  but we've got lyme and mold allergy so it affects us greatly.

  I have been doing mold remediation the past few months.  and I am planning

to do mold allergy desensitization.  I can give you more info regarding that if

you want.

> > > > > >

> > > > > > Blessings,

> > > > > > Roxanne

> > > > > >  

> > > > > >

> > > > > >

> > > > > > ________________________________

> > > > > > From: tim2buk <tim2buk@>

> > > > > > To: Lyme_and_Rife

> > > > > > Sent: Thursday, May 10, 2012 12:30 PM

> > > > > > Subject: OT: Hyperreaction to cold air

> > > > > >

> > > > > >

> > > > > >  

> > > > > > Hi all,

> > > > > >

> > > > > > Was wondering if anyone is experiencing an increase in symptoms

(headaches, post-nasal drip, fatigue)when you are in an air-conditioning draft

or even outside on a nice day, but with a cool breeze blowing. My situation is

so bad that I have to wear a hat even at 60 or 62 degrees, and I still get an

increase in symptoms. In the winter, I need to wear a hat & a hooded jacket but

I still have worsening symptoms still. It is one of my most severe problems

because it limits me to the point that I have become more home-bound because I

don't want to become sicker than I already am. We've had to stop going out to

eat because no matter where I sit, I am in a draft & I become so stressed out

because I know I am going to have big problems in the next few days. I know I

have low thyroid (Hashimoto's) but other people do too & don't have the severe

reactions that I do. Unfortunately, I have been on all thyroid meds there are &

none helped me, only made me feel

> > > > > > worse, so my doctor said not to take anything. My TSH is usually

around 3 or 4 (it's supposed to be around 1 or so). I've had tons of cortisol

saliva tests & mostly came back ok except for elevated night time saliva. I

feel that my adrenals must be shot but don't know what else to try for them

either. The glandulars make me nervous. Rhodiola helped me at one time, but

then it stopped giving me energy. I don't know if it is a lyme thing or what.

I just wanted to know if there is anybody else that is having these problems &

how you are dealing with them. Thanks for any thoughts.

> > > > > >

> > > > > > Susie

> > > > > >

> > > > >

> > > >

> > >

> >

>

[Guest guest]

Lena,

The bad part is that everything one tries makes them sicker & it takes too long

to be able to determine if you should stick with one method or move on. I know

it's pace not race, but it is still very difficult not to feel frustrated.

Thanks for the gentle reminder.

Susie

> > > > > >

> > > > > > Hi Susie,

> > > > > >

> > > > > > Forgot to mention one thing. Â I found out not too long ago

> that I have severe allergy to mold. Â that's why all the running nose/

> problems happens w/cold air. Â the mold allergy also severely weakens

> the immune system even more than lyme and coinfections. Â the weak

> immune system is why I think I got the staph and why I think its so

> hard to be in the cold air and feeling so ill the next days. Â

> > > > > >

> > > > > > I never knew I had mold in my place. Â I had/have no

> visible mold but now that I am more informed about mold, I am able to

> find it. Â For example, if you have any carpet in your place, you will

> imho have mold since carpet is a magnet for dust and dust is a magnet

> for mold. Â It doesn't affect people who don't have mold allergy or

> weakened immune system. Â so people don't pay attention to it. Â but

> we've got lyme and mold allergy so it affects us greatly. Â I have

> been doing mold remediation the past few months. Â and I am planning

> to do mold allergy desensitization. Â I can give you more info

> regarding that if you want.

> > > > > >

> > > > > > Blessings,

> > > > > > Roxanne

> > > > > > Â

> > > > > >

> > > > > >

> > > > > > ________________________________

> > > > > > From: tim2buk <tim2buk@>

> > > > > > To: Lyme_and_Rife

> > > > > > Sent: Thursday, May 10, 2012 12:30 PM

> > > > > > Subject: OT: Hyperreaction to cold air

> > > > > >

> > > > > >

> > > > > > Â

> > > > > > Hi all,

> > > > > >

> > > > > > Was wondering if anyone is experiencing an increase in

> symptoms (headaches, post-nasal drip, fatigue)when you are in an air-

> conditioning draft or even outside on a nice day, but with a cool

> breeze blowing. My situation is so bad that I have to wear a hat even

> at 60 or 62 degrees, and I still get an increase in symptoms. In the

> winter, I need to wear a hat & a hooded jacket but I still have

> worsening symptoms still. It is one of my most severe problems because

> it limits me to the point that I have become more home-bound because I

> don't want to become sicker than I already am. We've had to stop going

> out to eat because no matter where I sit, I am in a draft & I become

> so stressed out because I know I am going to have big problems in the

> next few days. I know I have low thyroid (Hashimoto's) but other

> people do too & don't have the severe reactions that I do.

> Unfortunately, I have been on all thyroid meds there are & none helped

> me, only made me feel

> > > > > > worse, so my doctor said not to take anything. My TSH is

> usually around 3 or 4 (it's supposed to be around 1 or so). I've had

> tons of cortisol saliva tests & mostly came back ok except for

> elevated night time saliva. I feel that my adrenals must be shot but

> don't know what else to try for them either. The glandulars make me

> nervous. Rhodiola helped me at one time, but then it stopped giving me

> energy. I don't know if it is a lyme thing or what. I just wanted to

> know if there is anybody else that is having these problems & how you

> are dealing with them. Thanks for any thoughts.

> > > > > >

> > > > > > Susie

> > > > > >

> > > > >

> > > >

> > >

> >

>

[Guest guest]

Often, our expectations make us judge any negative response as 'sicker' when actually, we're merely herxing, which feels lousy but isn't 'sicker' but an indication of progress that's not being supported by detox. If we drop that thing and pick up something else, without understanding, we're doomed to repeat this same mistake or compound it. That's why doing one's homework is so importantThis is why I do ONE thing at a time in the beginning, with at least a few weeks of careful observation of response to that one thing, mindful of detox methods and trying them if I feel 'sicker'. Then addition of a small amount of the next thing, watching carefully, will make it easy to figure out what did what.Before diagnosis, I dabbled in this and that, sometimes without learning (or remembering) some of the pertinent info, of listening to what people told me. My approach was emotional, inconsistent and haphazard, and I got myself into a hopeless muddle. As far as 'it takes too long'....Short cuts or short samplings of protocols will make it take longer, I promise you. Find one thing. Perhaps it doesn't really matter what it is, because not everything works for everyone and you just have to do the time on one thing at a time and work your way through your options. Tedious? Yes! Time-consuming? Yes! Focus. Stick with it, take notes, do detox and bide your time. Listen to others. Doubt your doubts; deal with what you know to be the self-sabotage of worrying yourself crazy.When you feel panic, do what you can to get grip; there are supplements that can help that. Review all the good advice that's already been given you. Panic will not serve this fight.Other protocols are promising: may even bring better results for you, just not all at one time just not all now. I know, it's maddening. but that's the way it is. There are STILL some protocols I'm eager to try, but I know they will have to wait. They're the aces up my sleeve. I simply mustn't do them now, because it will only confuse my issues. Two years ago, I tried LDN, which was supposed to help psoriatic arthritis and in a couple months, I had NEW outbreaks, on my face where there'd never been before! I stopped it. Now, two years later, I've made the burdened-liver/psoriasis-connection and reduced all of my patches with Milk Thistle (in the right amount rather than the token bits that made me think it was useless,) Now I've learned enough to realize that the LDN might actually have been working, but had also added more toxins to the liver, which made patches increase. Now, I might be prepared to try it again at some point, because it's great for reducing inflammation. All this takes experience, and the knowledge that brings. All this take time. All this takes time. All this takes time.Be well,Léna Lena, The bad part is that everything one tries makes them sicker & it takes too long to be able to determine if you should stick with one method or move on. I know it's pace not race, but it is still very difficult not to feel frustrated. Thanks for the gentle reminder. Susie > > > > > > > > > > > > Hi Susie, > > > > > > > > > > > > Forgot to mention one thing. Â I found out not too long ago > that I have severe allergy to mold. Â that's why all the running nose/ > problems happens w/cold air. Â the mold allergy also severely weakens > the immune system even more than lyme and coinfections. Â the weak > immune system is why I think I got the staph and why I think its so > hard to be in the cold air and feeling so ill the next days. Â > > > > > > > > > > > > I never knew I had mold in my place. Â I had/have no > visible mold but now that I am more informed about mold, I am able to > find it. Â For example, if you have any carpet in your place, you will > imho have mold since carpet is a magnet for dust and dust is a magnet > for mold. Â It doesn't affect people who don't have mold allergy or > weakened immune system. Â so people don't pay attention to it. Â but > we've got lyme and mold allergy so it affects us greatly. Â I have > been doing mold remediation the past few months. Â and I am planning > to do mold allergy desensitization. Â I can give you more info > regarding that if you want. > > > > > > > > > > > > Blessings, > > > > > > Roxanne > > > > > > Â > > > > > > > > > > > > > > > > > > ________________________________ > > > > > > From: tim2buk <tim2buk@> > > > > > > To: Lyme_and_Rife > > > > > > Sent: Thursday, May 10, 2012 12:30 PM > > > > > > Subject: OT: Hyperreaction to cold air > > > > > > > > > > > > > > > > > > Â > > > > > > Hi all, > > > > > > > > > > > > Was wondering if anyone is experiencing an increase in > symptoms (headaches, post-nasal drip, fatigue)when you are in an air- > conditioning draft or even outside on a nice day, but with a cool > breeze blowing. My situation is so bad that I have to wear a hat even > at 60 or 62 degrees, and I still get an increase in symptoms. In the > winter, I need to wear a hat & a hooded jacket but I still have > worsening symptoms still. It is one of my most severe problems because > it limits me to the point that I have become more home-bound because I > don't want to become sicker than I already am. We've had to stop going > out to eat because no matter where I sit, I am in a draft & I become > so stressed out because I know I am going to have big problems in the > next few days. I know I have low thyroid (Hashimoto's) but other > people do too & don't have the severe reactions that I do. > Unfortunately, I have been on all thyroid meds there are & none helped > me, only made me feel > > > > > > worse, so my doctor said not to take anything. My TSH is > usually around 3 or 4 (it's supposed to be around 1 or so). I've had > tons of cortisol saliva tests & mostly came back ok except for > elevated night time saliva. I feel that my adrenals must be shot but > don't know what else to try for them either. The glandulars make me > nervous. Rhodiola helped me at one time, but then it stopped giving me > energy. I don't know if it is a lyme thing or what. I just wanted to > know if there is anybody else that is having these problems & how you > are dealing with them. Thanks for any thoughts. > > > > > > > > > > > > Susie > > > > > > > > > > > > > > > > > > > > >

[Guest guest]

Hi Marie,I think psoriasis, like Lyme can be a very complex group of causes and issues. I've treated for many of them and one sort of patch recedes and another comes to fill the void. This time, however, whole areas have become completely clear, normal, with the proper amount of Milk Thistle supporting my liver. We'll see over time if this is the answer for me. Everyone's different. Be well,Léna Hi Lena I have read that psoriais was fungus, I hung on the lufeunron bu tincreased altitle bit th eodasge i guess I do nto absorb as well as ti should and i tis getting better each time now for me it is th etongu ethat tells me the most . It is much less white now withotu being yet ok it goe sin the right direction Kindly Marie To: Lyme_and_Rife Sent: Sunday, May 13, 2012 5:58 PMSubject: Re: Re: OT: Rifing for mold (was Hyperreaction to cold air) Often, our expectations make us judge any negative response as 'sicker' when actually, we're merely herxing, which feels lousy but isn't 'sicker' but an indication of progress that's not being supported by detox. If we drop that thing and pick up something else, without understanding, we're doomed to repeat this same mistake or compound it. That's why doing one's homework is so important This is why I do ONE thing at a time in the beginning, with at least a few weeks of careful observation of response to that one thing, mindful of detox methods and trying them if I feel 'sicker'. Then addition of a small amount of the next thing, watching carefully, will make it easy to figure out what did what. Before diagnosis, I dabbled in this and that, sometimes without learning (or remembering) some of the pertinent info, of listening to what people told me. My approach was emotional, inconsistent and haphazard, and I got myself into a hopeless muddle. As far as 'it takes too long'.... Short cuts or short samplings of protocols will make it take longer, I promise you. Find one thing. Perhaps it doesn't really matter what it is, because not everything works for everyone and you just have to do the time on one thing at a time and work your way through your options. Tedious? Yes! Time-consuming? Yes! Focus. Stick with it, take notes, do detox and bide your time. Listen to others. Doubt your doubts; deal with what you know to be the self-sabotage of worrying yourself crazy.When you feel panic, do what you can to get grip; there are supplements that can help that. Review all the good advice that's already been given you. Panic will not serve this fight. Other protocols are promising: may even bring better results for you, just not all at one time just not all now. I know, it's maddening. but that's the way it is. There are STILL some protocols I'm eager to try, but I know they will have to wait. They're the aces up my sleeve. I simply mustn't do them now, because it will only confuse my issues. Two years ago, I tried LDN, which was supposed to help psoriatic arthritis and in a couple months, I had NEW outbreaks, on my face where there'd never been before! I stopped it. Now, two years later, I've made the burdened-liver/psoriasis-connection and reduced all of my patches with Milk Thistle (in the right amount rather than the token bits that made me think it was useless,) Now I've learned enough to realize that the LDN might actually have been working, but had also added more toxins to the liver, which made patches increase. Now, I might be prepared to try it again at some point, because it's great for reducing inflammation. All this takes experience, and the knowledge that brings. All this take time. All this takes time. All this takes time. Be well, Léna Lena,The bad part is that everything one tries makes them sicker & it takes too long to be able to determine if you should stick with one method or move on. I know it's pace not race, but it is still very difficult not to feel frustrated. Thanks for the gentle reminder.Susie> > > > > >> > > > > > Hi Susie,> > > > > >> > > > > > Forgot to mention one thing. Â I found out not too long ago > that I have severe allergy to mold. Â that's why all the running nose/ > problems happens w/cold air. Â the mold allergy also severely weakens > the immune system even more than lyme and coinfections. Â the weak > immune system is why I think I got the staph and why I think its so > hard to be in the cold air and feeling so ill the next days. Â> > > > > >> > > > > > I never knew I had mold in my place. Â I had/have no > visible mold but now that I am more informed about mold, I am able to > find it. Â For example, if you have any carpet in your place, you will > imho have mold since carpet is a magnet for dust and dust is a magnet > for mold. Â It doesn't affect people who don't have mold allergy or > weakened immune system. Â so people don't pay attention to it. Â but > we've got lyme and mold allergy so it affects us greatly. Â I have > been doing mold remediation the past few months. Â and I am planning > to do mold allergy desensitization. Â I can give you more info > regarding that if you want.> > > > > >> > > > > > Blessings,> > > > > > Roxanne> > > > > > Â> > > > > >> > > > > >> > > > > > ________________________________> > > > > > From: tim2buk <tim2buk@>> > > > > > To: Lyme_and_Rife > > > > > > Sent: Thursday, May 10, 2012 12:30 PM> > > > > > Subject: OT: Hyperreaction to cold air> > > > > >> > > > > >> > > > > > Â> > > > > > Hi all,> > > > > >> > > > > > Was wondering if anyone is experiencing an increase in > symptoms (headaches, post-nasal drip, fatigue)when you are in an air- > conditioning draft or even outside on a nice day, but with a cool > breeze blowing. My situation is so bad that I have to wear a hat even > at 60 or 62 degrees, and I still get an increase in symptoms. In the > winter, I need to wear a hat & a hooded jacket but I still have > worsening symptoms still. It is one of my most severe problems because > it limits me to the point that I have become more home-bound because I > don't want to become sicker than I already am. We've had to stop going > out to eat because no matter where I sit, I am in a draft & I become > so stressed out because I know I am going to have big problems in the > next few days. I know I have low thyroid (Hashimoto's) but other > people do too & don't have the severe reactions that I do. > Unfortunately, I have been on all thyroid meds there are & none helped > me, only made me feel> > > > > > worse, so my doctor said not to take anything. My TSH is > usually around 3 or 4 (it's supposed to be around 1 or so). I've had > tons of cortisol saliva tests & mostly came back ok except for > elevated night time saliva. I feel that my adrenals must be shot but > don't know what else to try for them either. The glandulars make me > nervous. Rhodiola helped me at one time, but then it stopped giving me > energy. I don't know if it is a lyme thing or what. I just wanted to > know if there is anybody else that is having these problems & how you > are dealing with them. Thanks for any thoughts.> > > > > >> > > > > > Susie> > > > > >> > > > >> > > >> > >> >>