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I got pnumonia 3x last winter. I could tell by the deep cough that I had it before I even went in. I got the pnumonia shot this Fall and made it thru winter w/out getting it (but did get bronchitis!)

Stacey in MA

pneumonia

I have pneumonia. Woke up the other night with a high fever and chills and went to the ER. But did not even think of pneumonia and I even refused the chest x-ray at first until all of the other tests came back negative (I've had over 100 chest x-rays in the past 16 years and then developed breast cancer, so I don't let them do routine x-rays anymore). They did one film and they said right away I have pneumonia.It's weird because I just don't have many respiratory symptoms! Anyone ever had pneumonia with few symptoms? Well at least I don't feel that bad, just very tired.Lori

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Lori

Rest well and feel better soon...

Maybe you're so used to having severe respiratory symptoms that what seems mild to you could be notable to someone else?

I've been told a couple of times I had viral pneumonia (usually at the coughing up blood phase) but the chest xrays didn't show it.

Liz truelori <lori@...> wrote:

I have pneumonia. Woke up the other night with a high fever and chills and went to the ER. But did not even think of pneumonia and I even refused the chest x-ray at first until all of the other tests came back negative (I've had over 100 chest x-rays in the past 16 years and then developed breast cancer, so I don't let them do routine x-rays anymore). They did one film and they said right away I have pneumonia.It's weird because I just don't have many respiratory symptoms! Anyone ever had pneumonia with few symptoms? Well at least I don't feel that bad, just very tired.Lori

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Hi Lori and Liz,

I too have just been diagnosed as having pneumonia. I had a cold on hols, but still went in the v cold sea every day (pressure from my kids!). When I got home I started to feel very unwell and had an awful, deep cough. The mistake I made was thinking "oh no, another bad chest infection" and taking antibiotics that were in my cupboard, and not seeing my GP. The ab's helped, but I became worse when I finished the course. Pressure from hubby and freinds made me go to the doctors who said my temp was high and that I had pneumonia! I'm now on more antibiotics. The thing is that I thought I may have had it, but was waiting for the bad pain -I had a dull ache between my shoulderblades a nasty compulsive cough, and horrid frothy stuff from my lungs, felt very dizzy and weak, totally lost my appetite, etc, but was expecting awful pain. If that had happened, I would have been straight to the doctors. I've had pleuracy lots of times and even broken ribs from bad coughs, but never

pneumonia before. I wish I'd have known earlier so I would have been allowed to rest, but no chance!!

I think it's definately true that we are so used to having to cope with nasty infections while carrying on with life (in my case looking after 3 young children, studying, trying to move house and so on) that we just carry on regardless. If I rested or stayed in bed (fat chance) when ill, then I would have no life at all.

Becky Boston <elizabethboston@...> wrote:

Lori

Rest well and feel better soon...

Maybe you're so used to having severe respiratory symptoms that what seems mild to you could be notable to someone else?

I've been told a couple of times I had viral pneumonia (usually at the coughing up blood phase) but the chest xrays didn't show it.

Liz truelori <lori@...> wrote:

I have pneumonia. Woke up the other night with a high fever and chills and went to the ER. But did not even think of pneumonia and I even refused the chest x-ray at first until all of the other tests came back negative (I've had over 100 chest x-rays in the past 16 years and then developed breast cancer, so I don't let them do routine x-rays anymore). They did one film and they said right away I have pneumonia.It's weird because I just don't have many respiratory symptoms! Anyone ever had pneumonia with few symptoms? Well at least I don't feel that bad, just very tired.Lori

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  • 5 months later...

- our oldest daughter (13 non-PID) has had problems in the

last year with pneumonia. She's had it 4 times in 18 months. We were very

concerned that since she was entering puberty that her immune system was

going the way of her sister (CVID) and her dad (CVID). This summer her ped

gave her a Prevnar and tested her. She responded to all but 2. She just

seems prone right now to pneumonia. Maybe it's the age, maybe it's her

going going going all the time. She has taken Rocephin for each of her

pneumonias but her oxygen has only dropped once. We did daily Rocephin

shots (1.5 gms-several syringe shots) and an incentive spirometer at home

because she was so opposed to going into the hospital. The pneumonias

cleared each time. Right now she is battling a deep seeded sinus infection

and it is aggravating her heart. The ped started her on Omnicef yesterday

but she () refused a shot of Rocephin. So she's home from school again

today and is learning that the shot isn't all that bad. I told her she'd

feel like a new person if she'd just get it (it would just be the one 1 gm)

but she had so many last year she doesn't even want to hear the drug's name

anymore. During 's pneumonias Macey only got it once out of the 4.

Probably the one in the fall when the weather was fickle anyway and Macey

was just as suseptible as everyone else.

I hope she feels better soon and her breathing is better.

Ursula

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Thanks for all of the responses about Kelsey's pneumonia. I'm feeling much

less stressed about it now that I know that so many " healthy " kids get it

too. I did wonder if Kelsey could have scarlet fever, she's had it before

and she had strep just a couple of months ago. When she got sick with the

pneumonia, she never once complained of a sore throat and I even asked her a

couple of times if her throat hurt and she said it didn't. I do wonder

about her being a " strep carrier " and just wonder if this could have played

a role in this. The nurse came yesterday and showed me how to administer

the Rocephin via the IV. Not exactly a fun thing to do, I was so worried I

would mess it up, but I guess if I can do SCIG for months on end, I can do

this too! Anyway, thanks again for calming my nerves! Now I just to figure

out what we're going to do about school! She will be out for a minimum of

three weeks if she recovers quickly... that's a lot of homework!

Take care,

Mom to Conner (11, Asperger's, mild CP, partial seizures, asthma, GERD,

Hashimoto's disease, hypogammaglobulinemia, complement deficiency, antibody

deficiency, NK cell defect, and resolved adrenal insufficiency),

Hayden (11, PDD-NOS, IBS and moderate hearing loss/aided),

Evan (11, asthma and mild hearing loss/unaided),

and Kelsey - (9 going on 19!)

Please visit us at www.caringbridge.org/in/connersmith

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:

Our school district provides a free homebound tutor with 10 consecutive days

of absence. It's Illinois law. If you can start having a classmate nearby

bring home her work (when she's well enough to do it), you will probably not

have

to get really behind.

I am sorry it was so scary and am glad she's recovering. I thought the

sandpaper rash sounded " strep-y " too.

On a lighter note, I don't think I ever told you how very much I enjoyed your

previous signature line comment that Kelsey was " hearing... but not

listening! " . Loved it! :)

Good luck --

(mom to , age 6-1/2, dairy intolerant-related GERD -- currently

has polysaccharide antibody def, previously had transient IgG, IgA, t-cell &

other defs... and also to Kate, age 3!, more dairy intolerant but very healthy!)

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  • 3 weeks later...

>

> Bob,

>

> have you taken antibiotics in recent years? this will be

interesting to see how you react to them. I always feel better when

on them, some do, some don't. Let us know how you do!

I will. I haven't taken any in years. I took them then for my sinus

infection. I did feel better while on them but didn't last long and I

still have my sinus infection.

That reminds me, I tested positive for Lyme antigens and antibodies a

couple of years ago. the neurologist in Dallas gave me something

which I gave myself shots but I saw no improvement. I recently read a

book on Lyme Disease and it said there are no types of LD, one with

physical symptoms such as arthritis and the other was neuro symptoms.

The book said that Zithromax and others wouldn't work for the LD with

neuro symptoms. something was needed which penetrates nerve tissue

such as Rocephin IV and Ceftin orally. The book also said that most

people's immune system cannot fight off LD without help from

antibitoics. That would make me think that if we have antibodies then

we most likely have LD. The spirochettes would be inside out tissue

by now, wouldn't they? I wonder why doctors do not take some tissue

from somewhere and check it for disease also?

Bob

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Bob

That is called fungal pneumonia usually characterized by a milky white thick

mucous. As I recall you reported green, which suggests bacterial instead of

fungal, but the fungal may be lurking disguised.

mjh

In a message dated 12/23/2005 5:10:14 PM Eastern Standard Time,

blue74730@... writes:

My cough and lungs have not gotten any better though two days of abx

and breathing treatments. On the mold list I am on, several people

posted studies showing that mold can cause pneumonia. If I am not well

by Monday, I can go to my CFS doctor and talk with him about it. The

first few times I went to him about the mold, I got the look that he

didn't believe me. He would have to if a culture shows mold. I may

finally have some proof that mold is killing me in this mobile home.

My cousins's wife's son wants to rent it from me. He knows about the

mold but probably does not believe it either. He is about 33, wife

about the same and a 12 year old son. I don't want anyone else to get

ill.

Bob

mjh

" The Basil Book "

http://foxhillfarm.us/FireBasil/

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Bob,

I'm sure you know that not everyone gets ill from mold. Only a quarter

of the population has the bad mold gene, per Shoemaker. So I would not

assume that renters would become ill. And even if they have the bad

gene, if they are not already sick, the level of mold may not be high

enough to make them ill. There is toxic mold everywhere, I don't think

there are many people who actually live mold-free, other than the

extreme avoiders.

I think that self-diagnosing the cause of your pneumonia is a bit risky,

you could be wrong. It could be a bacteria that just needs a different

abx. But of course, the mold exposure weakens your immune, so maybe

everything is interrelated a bit. Have you been tested for mycoplasma?

I have a lot of related issues, carry mycoplasma pneumoniae, and get it

regularly when I get worn down. Pharmaceutical ABX did not work against

this for me. This is a strange illness (mycoplasma phneumonia). Some

non-traditional things that help me:

Heat over the bronchiole tubes and lungs (hot packs, or FIR lights if

you have those available, you can make a hot pack with rice and an

athletic sock). This can really help a lot, I think it even kills some

things and/or boosts immune strength. But not too hot, this is

sensitive tissue. I prefer mild heat for a longer time.

North pole magnets over the bronchiole tubes and lungs.

Inhale a high quality colloid silver. I just use a cheap atomizer

spray. Better would be a nebulizer. I have read that an all plastic

air brush (for painting) is the best (there is a website on this

somewhere, talking about how even the toughest cases of pneumonia are

treated successfully with nebulized CS).

Massive herbal immune-boosting and abx. I 'throw the kitchen sink' at

bronchitis/pneumonia, and that usually works, along with the other

measures. My natural treatments generally include GSE,

Echinacea/C/Zinc, Olive Leaf Extract, Oregano Oil, and sometimes I add

Cat's Claw (Samento). Also, this sometimes creates die-off herx, so I

also boost some detox supplements (whey protein, recancostat, bentonite

clay, phosphatidylcholine).

Also, loads of enzymes and extra salt (natural unprocessed sea salt

only) and vitamin C.

I realize you probably do not have all of this, but maybe you can get

some ideas. I really do have a bad situation with this, and these steps

have helped to control the problem. This is the infection that

activated my long-term Lyme and precipitated CFS. So it is my

'nemesis.' Sounds like it is one of your major battles as well. Good

luck!

--Kurt

SPAM-MED: Pneumonia

My cough and lungs have not gotten any better though two days of abx

and breathing treatments. On the mold list I am on, several people

posted studies showing that mold can cause pneumonia. If I am not well

by Monday, I can go to my CFS doctor and talk with him about it. The

first few times I went to him about the mold, I got the look that he

didn't believe me. He would have to if a culture shows mold. I may

finally have some proof that mold is killing me in this mobile home.

My cousins's wife's son wants to rent it from me. He knows about the

mold but probably does not believe it either. He is about 33, wife

about the same and a 12 year old son. I don't want anyone else to get

ill.

Bob

This list is intended for patients to share personal experiences with

each other, not to give medical advice. If you are interested in any

treatment discussed here, please consult your doctor.

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Hi Bob

See if your doctor will call Shoemaker for a consult. Many of the doctors

treating mold learned by consulting Shoemaker. He could say he has a patient

who has CFS and is very mold sensitive, and now has pneumonia symptoms. I'm

sure within 5 minutes Shoemaker could give some suggestions.

As someone said, only 24% of the population is sensitive to mold problems. And

I don't think something dramatic could happen suddenly. They could live there,

but just warn them that if someone starts to get sick then they should

investigate the mold angle or move out.

Doris

Pneumonia

My cough and lungs have not gotten any better though two days of abx

and breathing treatments. On the mold list I am on, several people

posted studies showing that mold can cause pneumonia. If I am not well

by Monday, I can go to my CFS doctor and talk with him about it. The

first few times I went to him about the mold, I got the look that he

didn't believe me. He would have to if a culture shows mold. I may

finally have some proof that mold is killing me in this mobile home.

My cousins's wife's son wants to rent it from me. He knows about the

mold but probably does not believe it either. He is about 33, wife

about the same and a 12 year old son. I don't want anyone else to get

ill.

Bob

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>

>

>

> Bob

>

> That is called fungal pneumonia usually characterized by a milky

white thick

> mucous. As I recall you reported green, which suggests bacterial

instead of

> fungal, but the fungal may be lurking disguised.

>

> mjh

Someone else also wrote me that greenish suggests bacterial. I have

today's pill and tomorrow left and someone said they work for five days

after so I will know. I am making plans in my head of where I could go

if I need to leave though.

Bob

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Good luck with that! Thats not good. Mobile homes can be tough

environments;lots of synthetics, lots of potential for mold. Some people can

tolerate that some can't. I certainly couldn't. I guess you're in Texas? If

you have the money and can see Dr. Rea in Dallas he knows all about mold and can

help. This is just guessing but it might be good to get into a sauna and really

heat things up - thats done wonders with me with some minor colds in the past.

Cort

Bob <blue74730@...> wrote:

My cough and lungs have not gotten any better though two days of abx

and breathing treatments. On the mold list I am on, several people

posted studies showing that mold can cause pneumonia. If I am not well

by Monday, I can go to my CFS doctor and talk with him about it. The

first few times I went to him about the mold, I got the look that he

didn't believe me. He would have to if a culture shows mold. I may

finally have some proof that mold is killing me in this mobile home.

My cousins's wife's son wants to rent it from me. He knows about the

mold but probably does not believe it either. He is about 33, wife

about the same and a 12 year old son. I don't want anyone else to get

ill.

Bob

This list is intended for patients to share personal experiences with each

other, not to give medical advice. If you are interested in any treatment

discussed here, please consult your doctor.

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Hi Bob,

Have you looked into housing in Wimberley, Texas?

There are a lot of people with MCS there (near Austin). Dr. Rea's

office used to recommend that area for people with MCS.

I did a Google search on " multiple chemical sensitivity MCS housing

Wimberley Texas " and got this group:

mcssafeshelterusa/

The description is:

Short-term and long-term housing for people with MCS (Multiple Chemical

Sensitivity). Check our database for listings by state. (Please use the

two-digit code.)

In the Database, there is a listing for a room in an EI's

(environmental illness) house in Euless, Tx. There is also a listing

for trailers or mobile homes for sale or rent that are suitable for MCS.

I know this is a long shot, but it might lead to something eventually.

***********

For many years in the mid-nineties, I had chronic bronchitis, asthma,

and even pneumonia. When I went to an allergy clinic to be tested for

allergies, they tested me for about 7 different molds, and I was

extremely allergic to all of them. A positive reaction to an allergy

test is usually a wheal about 1/4 to 1/2 inches in diameter. In my

case, my entire upper arm turned bright red, swollen and itchy. I was

told that desensitization therapy for mold would help some but not a

great deal. So I began the long process of reducing my exposure to

mold. We pulled up the carpets and painted the concrete floors, bought

3 Austin air filter machines with 3 types of filtering (charcoal, hepa,

and some other chemical) for people with MCS (the $400 model), and

replaced the air conditioning ducts with metal. We also caulked all

cracks, baseboards, etc. and tried to prevent any air from the attic or

inside the walls from getting into the house. Since then, I have not

had bronchitis, pneumonia, or asthma. The only two asthma attacks I

have had occurred when I was exposed to newspaper ink and a fabric

store (fabric finishers). But my house is still not as mold free as it

could be. (We ran out of money and energy before we could finish.) I

still react to mold inside one wall when it rains. I take Benadryl a

lot, and that keeps my mold reactions under control. There is no doubt

that mold reactions, whether allergic or toxic, can affect the lungs,

the brain, and probably the whole body.

NEEDS (needs.com) has started selling a a citrus product that is

supposed to be as effective as Chlorine for killing mold, without the

toxicity of Chlorine. But Citrus is a problem for some people.

I hope this provides some leads for finding help.

Vickie

>

> My cough and lungs have not gotten any better though two days of abx

> and breathing treatments. On the mold list I am on, several people

> posted studies showing that mold can cause pneumonia. If I am not

well

> by Monday, I can go to my CFS doctor and talk with him about it. The

> first few times I went to him about the mold, I got the look that he

> didn't believe me. He would have to if a culture shows mold. I may

> finally have some proof that mold is killing me in this mobile home.

>

> My cousins's wife's son wants to rent it from me. He knows about the

> mold but probably does not believe it either. He is about 33, wife

> about the same and a 12 year old son. I don't want anyone else to get

> ill.

>

> Bob

>

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hi bob , know your the expert sadly on mold fom ongong promblems with your

home..

i had pneumoia years ago and had to constantly change antibiotics till we

found the rite one that brought my low grade 99.6-9 fver down ...when i

went three days without change i went back and had them switch the

antibiotics as i fgured out for me it usually kicked in after three days

and was early intense cfids patient than..good luck with your housing ...

the worst thing i did was not rest enuf ...so it took me five years for a

normal chest x ray and have alot of scar tissue damage in my lungs now :(

...so maybe run it by your md

maybe their is some kind of prefab u can buy that u can tolearte ? or if

its summer in mexico or further down south why not use a good large tent on

campsite or trailer park ?

feel better , goodl luck

> [Original Message]

> From: Bob <blue74730@...>

> < >

> Date: 12/23/2005 5:09:59 PM

> Subject: Pneumonia

>

> My cough and lungs have not gotten any better though two days of abx

> and breathing treatments. On the mold list I am on, several people

> posted studies showing that mold can cause pneumonia. If I am not well

> by Monday, I can go to my CFS doctor and talk with him about it. The

> first few times I went to him about the mold, I got the look that he

> didn't believe me. He would have to if a culture shows mold. I may

> finally have some proof that mold is killing me in this mobile home.

>

> My cousins's wife's son wants to rent it from me. He knows about the

> mold but probably does not believe it either. He is about 33, wife

> about the same and a 12 year old son. I don't want anyone else to get

> ill.

>

> Bob

>

>

>

>

>

>

> This list is intended for patients to share personal experiences with

each other, not to give medical advice. If you are interested in any

treatment discussed here, please consult your doctor.

>

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I would be leery of Wimberly Texas. Althought it is a very cute place, it is

very close to San which has a terrible mold problem. In fact, it's

ironic that a lot of people with MCS live there. My MCS went away when I got

away from mold, which is what Shoemaker says has happened with over 500 patients

he had with MCS.

Doris

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

From: vickie77077

Have you looked into housing in Wimberley, Texas?

There are a lot of people with MCS there (near Austin). Dr. Rea's

office used to recommend that area for people with MCS.

I did a Google search on " multiple chemical sensitivity MCS housing

Wimberley Texas " and got this group:

mcssafeshelterusa/

The description is:

Short-term and long-term housing for people with MCS (Multiple Chemical

Sensitivity). Check our database for listings by state. (Please use the

two-digit code.)

In the Database, there is a listing for a room in an EI's

(environmental illness) house in Euless, Tx. There is also a listing

for trailers or mobile homes for sale or rent that are suitable for MCS.

I know this is a long shot, but it might lead to something eventually.

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>

> I would be leery of Wimberly Texas. Althought it is a very cute

place, it is very close to San which has a terrible mold

problem.

Doris,

all the way from the Gulf Coast up through Oklahoma is has very high

mold spores in the air from high humidity. I agree with Doris that once

we get away from mold, our MCS will get better. I am hearing that from

two friends. I suspect that many PWC's live in areas with high mold

spore counts and even in their homes.It is really everywhere in humid

places. I wouldn't want to buy a travel trailer made in Dallas. It

would already have mold in it, maybe not bad but for me, it does not

take much.

Bob

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  • 1 month later...
Guest guest

If it's bacterial pneumonia " they " will prescribe antibiotics.

Who has it? A child or adult?

Sheri B.

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

Relax. virus scanning helps detect nasty viruses!

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Adult. My mother

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

If it's bacterial pneumonia " they " will prescribe antibiotics.

Who has it? A child or adult?

Sheri B.

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Guest guest

At 10:38 AM 3/1/2006 -0500, you wrote:

>Adult. My mother

>

Will she see a homeopath?

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

>

>

>If it's bacterial pneumonia " they " will prescribe antibiotics.

> Who has it? A child or adult?

> Sheri B.

>

> >

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Vaccination Information & Choice Network, Nevada City CA & Wales UK

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Guest guest

" They " will more than likely prescribe antibiotics even if it isn't

bacterial. " They " will probably give some line about how since they

don't know for sure what type it is, that antibiotics would be

the " best " course of treatment, just to be on the " safe side " .

>

> If it's bacterial pneumonia " they " will prescribe antibiotics.

> Who has it? A child or adult?

> Sheri B.

>

>

> ---------------------------------

> Relax. virus scanning helps detect nasty viruses!

>

>

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Guest guest

Jen,

My folks are the same way, although my dad is finally getting fed up with

seeing no results from his docs. He is on the verge of MAYBE seeing a

homeopath.

Still, today, when I asked him what he had to lose he said, " $300 or $400 -

that's all. " To which I replied, " well, if your health isn't worth that then

why don't you just go sit in the woods and wait for the wolves. " He wasn't

thrilled with that comment but hey - reality bites, right?

Sheri B.

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

Bring photos to life! New PhotoMail makes sharing a breeze.

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Guest guest

So true. It is so sad. I keep praying that they will open their eyes:)

jen c

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

Jen,

My folks are the same way, although my dad is finally getting fed up with

seeing no results from his docs. He is on the verge of MAYBE seeing a

homeopath.

Still, today, when I asked him what he had to lose he said, " $300 or $400

- that's all. " To which I replied, " well, if your health isn't worth that

then why don't you just go sit in the woods and wait for the wolves. " He

wasn't thrilled with that comment but hey - reality bites, right?

Sheri B.

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  • 2 weeks later...
Guest guest

Chonette,

Like you said, it happened so quickly, I had a cold for a few days that was

slowly getting worse, that like so many colds was uncomfortable but not

seemingly bad more than any other cold. Then one night I went to sleep and woke

in the middle of the night and I was choking because I couldn't get any air into

my lungs and I had to sit on the edge of the bed and force myself to breath in

and out slowly until I cought my breath again, but this time I could barely

breath in or out, the lungs had no capacity, it happened so quickly.....but then

of course I went, but not till the next morning......next time I will go right

then in the middle of the night. It's a bit scary when you literally can't

breath. I think I have been lucky, but in fact I am still very weak,

haven't left the house in 10 days except going to the doctor and right now I

can't walk around without having a hard time breathing, still coughing up flem

from inside my lungs and it's going to be another week before I can leave the

house I am sure. It makes you very weak also.

Ok, I got up for some cough syrup so I am heading back to bed. Good luck to

all my blood brothers and sisters who are in treatment, give em hell! Kurt

--------- Re: r-hdmp

Also Andy, I am taking it very carefully with the pneumonia, the worst of it

is over, but it was touch and go for awhile, it's amazing how you get to the

point where you can hardly breath in or out.....your lungs just fill up with

fluid, it definitely gets your attention. Now my lunds are clearing up,

and I can breath easily again. Now I understand when they say that the

majority of people with CLL die of Pneumonia. With a weakened immune

system there is no way to fight it off.

I caught this cold from my Dad and I was trying to tough it out because I

don't want to use too many antibiotics so that I become immune to

them....well I almost didn't get a chance to use the immunity I was trying

to save. Doc said, next time I get a cold or flu to always have it checked

and take antibiotic most of the time.

So as a lesson to all of you, go get yourselves checked when you get a

cold, it's a pain in the butt always running to the doc, but believe me

pneumonia is nothing to play with.

Ok, hope all are having a good sunday. K.

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My pulmonologist has put me on daily Bactrim in hopes

that it will prevent pneumonia. It has cleared up my

cough. I am thinking of you,m Kurt, with deep

fondness; we have been correspondents a long time!

Carolyn

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Kurt,

I hope you are feeling better, your experience is a good example for all of

us, how something can get so bad in just a few hours, I guess only when we

have lived the experience ourselves or in our household we know the

consequences and we do not allow a next time.

with fondness affection and a big hug, I hope you get better soon.

Chonette

> Message: 7

> Date: Wed, 15 Mar 2006 12:06:24 +0000

> From: thel.g@...

> Subject: Re: pneumonia

>

> Chonette,

>

> Like you said, it happened so quickly, I had a cold for a few days that

was slowly getting worse, that like so many colds was uncomfortable but not

seemingly bad more than any other cold. Then one night I went to sleep and

woke in the middle of the night and I was choking because I couldn't get any

air into my lungs and I had to sit on the edge of the bed and force myself

to breath in and out slowly until I cought my breath again, but this time I

could barely breath in or out, the lungs had no capacity, it happened so

quickly.....but then of course I went, but not till the next

morning......next time I will go right then in the middle of the night.

It's a bit scary when you literally can't breath. I think I have been

lucky, but in fact I am still very weak, haven't left the house in 10 days

except going to the doctor and right now I can't walk around without having

a hard time breathing, still coughing up flem from inside my lungs and it's

going to be another week before I can leave the house I am sure. It makes

you very weak also.

>

> Ok, I got up for some cough syrup so I am heading back to bed. Good

luck to all my blood brothers and sisters who are in treatment, give em

hell! Kurt

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