Skin sores

[Guest guest]

Hi Ersilia,

I have them too, and they're known as pretibial myxedema. This condition

generally affects the front part of the lower legs. Cortisone cream has

helped, and I also use an herbal salve now and then. Elaine

[Guest guest]

Hi

I had sores (very itchy). They had a definite centre. There was

nothing to do but live through them. They were diagnosed as Pitiriasis

Rosea. They seem to happen fairly frequently from what I understand.

They went away on their own but came back again! The second time they

lasted about 5 weeks then went. Haven't had any further.

Check it out with your doctor.

Kate

ccdream@... wrote:

>

>

> Hi all,

> would like to know what you all do for the skin sores ?

> I am hyperT.

> Do any of you get the itchy sores ? usually only the one found on the

> leg.

> but now i have 2 of them, they look like ringworm sores, but of course

> they

> arnt ringworm sores.

>

> --

>

> Ersilia ^

> Sydney Australia (*.*)~~~

> `````

[Guest guest]

Sammy gets patches of eczema as well. Not all the time, and usually just on

her back, but she's had it off and on since she was about two. Over the

counter Cortaid (cortisone cream) works great.

--Lori (mom to Sammy, 6, JRA/uveitis/?)

[Guest guest]

My daughter gets goose bumps a lot of time with the fever, but no rash.

magoo3153 <magoo3153@...> wrote: Does anyone experiemce sores on

their childs body? My daughter has

been getting sores on her chest area, back of neck, bottom, and all

over her trunk of body. In the beginning it looks like ring worm but

its not, and the doctors here say its dry skin patches but this is

definetly not dry skin. Any ifo would be great. My daughter was on

cimitdine for 8 months and we have stopped and been fever free for 2

months. But now the sores any connections?

Thanks

LAurie mom of 6 yrs old

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

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[Guest guest]

HI,

This does NOT seem to be a sympto. May be totally unrelated.

Your post is the post mentioning actual sores all over the body since I started

this group back in early 2000.

God Bless

Fran

Fran Bulone RN

Mom to ph 7yr

Waxhaw NC

/

[Guest guest]

My five year old had this . . . he had tons of ringworm looking spots

on his legs, chests, arms etc. It was gross. I was freaking out

wondering how he came into contact with it. I was putting Lotrimim on

his spots 3 times a day and it wasn't working. I took him to the Ped

and they said that it was exsema (spelt way wrong) and so I put

steriod cream on it and they went away! There is a exsema that is

round like ringworm - maybe this is what she has . . .

Hannah

>

> Does anyone experiemce sores on their childs body? My daughter has

> been getting sores on her chest area, back of neck, bottom, and all

> over her trunk of body. In the beginning it looks like ring worm

but

> its not, and the doctors here say its dry skin patches but this is

> definetly not dry skin. Any ifo would be great. My daughter was on

> cimitdine for 8 months and we have stopped and been fever free for 2

> months. But now the sores any connections?

> Thanks

> LAurie mom of 6 yrs old

>

[Guest guest]

My daughter has periodical fevers(since she was 1 yr and 3 months) and

excema(since she was 8 months). Are these related somehow ? Also she started

getting the fevers since her MMR shots (at age 1). could the fevers be due to

the vaccinations ? Just trying to understand the cause.

LoriToomey@... wrote: Sammy gets patches of eczema as well. Not all

the time, and usually just on

her back, but she's had it off and on since she was about two. Over the

counter Cortaid (cortisone cream) works great.

--Lori (mom to Sammy, 6, JRA/uveitis/?)

[Guest guest]

If the original person is describing eczema, this is common with many PFSs.

Actual SORES are NOT common. There is a difference. ph also has eczema,

worse as infant and toddler and better now.

Fran

Fran Bulone RN

Mom to ph 7yr

Waxhaw NC

/

[Guest guest]

PFS is NOT from vaccinations. There is no medical documentation. There appears

to be VARIOUS things that may be a trigger the start of however not one

simple answer. Children get their first episode at various ages not

specific to any vaccine or specific trigger.

Also there is a message board out on for people who feel vaccines may be

the cause. Please join that group if you would like to discuss this issue.

FranFran Bulone RN

Mom to ph 7yr

Waxhaw NC

/

[Guest guest]

In a message dated 8/5/2006 5:06:23 A.M. Eastern Standard Time,

fbulone@... writes:

If the original person is describing eczema, this is common with many PFSs.

Actual SORES are NOT common. There is a difference. ph also has

eczema, worse as infant and toddler and better now.

I did not know that eczema was common in PFS's. Nicky has had eczema ever

since I can remember, Fortunately we got it under control last year and seem

to have a good handle on it this year.

[Guest guest]

Hello.

I don't have enough time to read all the posts and emails on this

group, but check them from time to time (I get the digest). I

happened to read the post about the skin sores and thought I'd report

my own experience.

On Aug. 13, 2006, after working in the garden most of the day, I came

inside and felt like something stung me on my left shoulder. I saw

nothing there, but the pain was severe and it began to itch, burn and

sting madly. I tried topical applications of ointments, salves,

essential oils, colloidal silver, aloe vera, cortisone cream, anti-

fungal, ice, heat, you name it. The pain was deep, relentless and

persistent. It continued into the night such that I couldn't even

sleep. The next day I found 2 small crater sores on the spot. I

thought I'd been bitten by some sort of spider, but the craters were

not close together, about an inch or so apart. I thought the worst

was over.

From then on, every night, the cycle repeated itself and more sores

appeared and spread down my arm. Internet research led me to rule

out shingles, but I thought it might be scabies. I treated for

scabies, but that did not solve the problem. I developed huge scabs

from scratching. After a month of suffering, I went to see my doc at

Kaiser who looked at the sores and even took a scraping to look at

under a microscope. He said it didn't look like scabies at all, but

he had no idea what it was and went ahead and prescribed permethrin

cream anyway (which I did not use because I have Hep C). I have also

been exposed to mold which is why I was referred to join this group.

The torture continued and led me to find out about Morgellons which

is what I believe it is. But what Morgellons is, remains a mystery

although many theories abound. I joined many Morg. groups looking

for solutions and relief. In doing so, I also learned that there was

a connection between the Morg. symptoms and Lyme disease. I soon

found out that I had Lyme and Babesia to add to my nightmare. I'm

not sure what the most current and up to date findings are regarding

Morgellons, but I'm convinced that it is some sort of parasite as it

cycles with the lunar phases with outbreaks at new and full moons

(parasites reproduce with the lunar cycles). The sores (craters)

appear and open up without any scratching or provocation and tiny

seedlike grains come out of them. I looked at these under a friend's

microscope and they look like they have a cell wall with blue fibers

resembling malphigian tubules within. Some of them had a fiber

attached to them. I was totally freaked out and being driven mad by

this...saving the extrusions in little vials. Out of fear of being

labeled with the dx of delusional parasitosis, I never went back to

see my Kaiser doctor about this as I've heard too many horror tales

of going down that road.

After trying many suggestions and treatments for the Morgellon sores

which would not heal and had spread to the right shoulder, arm and

back of neck and shoulders, I heard about NutraSilver. I took it as

part of a trial and within a wk., experienced improvement. It did

not cure or prevent the condition entirely, but mitigated the spread

and severity of the outbreaks as long as I kept taking it. You do

not apply it topically, but take it internally. If I put it on the

sores topically, the critters or whatever the hell they are under the

skin just migrate to a new spot and spread (very painful). I could

actually see the tunnels under my skin as faint white lines. I

currently take 30 drops of NS in a big glass of water 2x/day. As

long as I do this, the outbreaks that occur (always with the new and

full moons), are one to two small sores that quickly heal...still in

the same regions of the initial outbreaks. If I stop taking NS, all

hell breaks loose quickly and the sores spread. Last year, I had

pancreatitis and couldn't take any of my supplements for over a

couple wks. as I was too ill and could barely drink water and eat at

all. During this time, I experienced an outbreak of painful lesions

equivalent to the first time and it spread rapidly down my right

arm. One of the sores became infected and left a huge scar. After

being able to resume taking supplements again including NS, the sores

abated and healed. Thus, I keep taking NS and it keeps things from

getting out of control.

Being that I have Hep C, Lyme, Babesia and this Morg. nightmare, my

life is very complicated and stretched with protocols and such, thus

I'm not able to keep up with the emails and groups, so I can't

promise I'll be able to respond should anyone reply to me about this

in a timely manner. I will just leave things like this: Nutrasilver

is what is working for me to mitigate the severity of the Morg.

sores. No cure, but control and relief. Being that I have liver

issues, I know I can't experiment with some of the stuff others have

used and found to be helpful such as ivermectin and fenbendazole

(wormers)...much too toxic for me. I've been taking NS regularly now

since 2006 with the exception of the pancreatitis episode and one

other time when I thought I'd try to stop and see what happened which

wasn't a good idea at all. I've used other colloidal silvers for

years and they were not effective with this condition. Only NS has

worked for me. I have no fear of using colloidal silvers as long as

the particle size in nano-sized.

Good luck to you and healing.

in Sacramento

[Guest guest]

wow, it just leaves me speechless. so sorry you are going through

this.

--- In , " Ostoich " <jostoich@...>

wrote:

>

> Hello.

>

> I don't have enough time to read all the posts and emails on this

> group, but check them from time to time (I get the digest). I

> happened to read the post about the skin sores and thought I'd

report

> my own experience.

>

> On Aug. 13, 2006, after working in the garden most of the day, I

came

> inside and felt like something stung me on my left shoulder. I saw

> nothing there, but the pain was severe and it began to itch, burn

and

> sting madly. I tried topical applications of ointments, salves,

> essential oils, colloidal silver, aloe vera, cortisone cream, anti-

> fungal, ice, heat, you name it. The pain was deep, relentless and

> persistent. It continued into the night such that I couldn't even

> sleep. The next day I found 2 small crater sores on the spot. I

> thought I'd been bitten by some sort of spider, but the craters

were

> not close together, about an inch or so apart. I thought the worst

> was over.

>

> From then on, every night, the cycle repeated itself and more sores

> appeared and spread down my arm. Internet research led me to rule

> out shingles, but I thought it might be scabies. I treated for

> scabies, but that did not solve the problem. I developed huge

scabs

> from scratching. After a month of suffering, I went to see my doc

at

> Kaiser who looked at the sores and even took a scraping to look at

> under a microscope. He said it didn't look like scabies at all,

but

> he had no idea what it was and went ahead and prescribed permethrin

> cream anyway (which I did not use because I have Hep C). I have

also

> been exposed to mold which is why I was referred to join this group.

>

> The torture continued and led me to find out about Morgellons which

> is what I believe it is. But what Morgellons is, remains a mystery

> although many theories abound. I joined many Morg. groups looking

> for solutions and relief. In doing so, I also learned that there

was

> a connection between the Morg. symptoms and Lyme disease. I soon

> found out that I had Lyme and Babesia to add to my nightmare. I'm

> not sure what the most current and up to date findings are

regarding

> Morgellons, but I'm convinced that it is some sort of parasite as

it

> cycles with the lunar phases with outbreaks at new and full moons

> (parasites reproduce with the lunar cycles). The sores (craters)

> appear and open up without any scratching or provocation and tiny

> seedlike grains come out of them. I looked at these under a

friend's

> microscope and they look like they have a cell wall with blue

fibers

> resembling malphigian tubules within. Some of them had a fiber

> attached to them. I was totally freaked out and being driven mad

by

> this...saving the extrusions in little vials. Out of fear of being

> labeled with the dx of delusional parasitosis, I never went back to

> see my Kaiser doctor about this as I've heard too many horror tales

> of going down that road.

>

> After trying many suggestions and treatments for the Morgellon

sores

> which would not heal and had spread to the right shoulder, arm and

> back of neck and shoulders, I heard about NutraSilver. I took it

as

> part of a trial and within a wk., experienced improvement. It did

> not cure or prevent the condition entirely, but mitigated the

spread

> and severity of the outbreaks as long as I kept taking it. You do

> not apply it topically, but take it internally. If I put it on the

> sores topically, the critters or whatever the hell they are under

the

> skin just migrate to a new spot and spread (very painful). I could

> actually see the tunnels under my skin as faint white lines. I

> currently take 30 drops of NS in a big glass of water 2x/day. As

> long as I do this, the outbreaks that occur (always with the new

and

> full moons), are one to two small sores that quickly heal...still

in

> the same regions of the initial outbreaks. If I stop taking NS,

all

> hell breaks loose quickly and the sores spread. Last year, I had

> pancreatitis and couldn't take any of my supplements for over a

> couple wks. as I was too ill and could barely drink water and eat

at

> all. During this time, I experienced an outbreak of painful

lesions

> equivalent to the first time and it spread rapidly down my right

> arm. One of the sores became infected and left a huge scar. After

> being able to resume taking supplements again including NS, the

sores

> abated and healed. Thus, I keep taking NS and it keeps things from

> getting out of control.

>

> Being that I have Hep C, Lyme, Babesia and this Morg. nightmare, my

> life is very complicated and stretched with protocols and such,

thus

> I'm not able to keep up with the emails and groups, so I can't

> promise I'll be able to respond should anyone reply to me about

this

> in a timely manner. I will just leave things like this:

Nutrasilver

> is what is working for me to mitigate the severity of the Morg.

> sores. No cure, but control and relief. Being that I have liver

> issues, I know I can't experiment with some of the stuff others

have

> used and found to be helpful such as ivermectin and fenbendazole

> (wormers)...much too toxic for me. I've been taking NS regularly

now

> since 2006 with the exception of the pancreatitis episode and one

> other time when I thought I'd try to stop and see what happened

which

> wasn't a good idea at all. I've used other colloidal silvers for

> years and they were not effective with this condition. Only NS has

> worked for me. I have no fear of using colloidal silvers as long

as

> the particle size in nano-sized.

>

> Good luck to you and healing.

> in Sacramento

>