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Dr. Marinkovich

Redwood City, CA

He's educated at Stanford.

One of the first doctors to identify and treat mold illness.

Some say he's one of the best in the country.

People do fly in to see him and be treated.

Very nice, soft spoken man.

He's helped me.

Angelika

[] markinvoch

> Can someone tell me who this is? She/he is an MD, ND?

>

> Bobbie

>

>

>

>

>

>

>

>

> FAIR USE NOTICE:

>

>

>

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Angelika:

Does Dr. Marinkovich have a website? If so please share.

I don't have plans to fly to CA and consult with him; would be interested to

learn more of his protocols.

Thanks so much,

Rosie

> Dr. Marinkovich

> Redwood City, CA

>

> He's educated at Stanford.

> One of the first doctors to identify and treat mold illness.

> Some say he's one of the best in the country.

> People do fly in to see him and be treated.

> Very nice, soft spoken man.

> He's helped me.

>

> Angelika

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In a message dated 10/7/2005 8:58:31 PM Pacific Standard Time,

moldhelp@... writes:

Dr. Marinkovich

Redwood City, CA

He's educated at Stanford.

One of the first doctors to identify and treat mold illness.

Some say he's one of the best in the country.

People do fly in to see him and be treated.

Very nice, soft spoken man.

He's helped me.

Angelika

Dr. Marinkovich helped me, too. He treats from an immunological standpoint

while Dr. Shoemaker treats from a toxicological standpoint. Both men are

seeing great success with their patients.

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In a message dated 10/8/2005 6:57:43 AM Pacific Standard Time,

realmoldygal@... writes:

What does he use to treat mold illness?

Bobbie

Avoidance, antifungal nasal (like the Mayo Clinic) and/or oral medication/

mold free diets.

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What does he use to treat mold illness?

Bobbie

--- In , " Angelika \(mold list\) " <moldhelp@p...>

wrote:

>

> Dr. Marinkovich

> Redwood City, CA

>

> He's educated at Stanford.

> One of the first doctors to identify and treat mold illness.

> Some say he's one of the best in the country.

> People do fly in to see him and be treated.

> Very nice, soft spoken man.

> He's helped me.

>

> Angelika

>

> [] markinvoch

>

>

> > Can someone tell me who this is? She/he is an MD, ND?

> >

> > Bobbie

> >

> >

> >

> >

> >

> >

> >

> >

> > FAIR USE NOTICE:

> >

> >

> >

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THE IDIOTS WHO SAY WE'RE WRONG SHOULD WORK ABOUT A MONTH IN MY FORMER PLACE

OF EMPLOYMENT...THEY'D GET A SNOOT FULL..... & THEN WE'D SEE IF THEY ARE

" BELIEVERS! "

VICTORIA :>(

Re: [] markinvoch

>

> In a message dated 10/7/2005 8:58:31 PM Pacific Standard Time,

> moldhelp@... writes:

>

> Dr. Marinkovich

> Redwood City, CA

>

> He's educated at Stanford.

> One of the first doctors to identify and treat mold illness.

> Some say he's one of the best in the country.

> People do fly in to see him and be treated.

> Very nice, soft spoken man.

> He's helped me.

>

> Angelika

>

>

> Dr. Marinkovich helped me, too. He treats from an immunological

> standpoint

> while Dr. Shoemaker treats from a toxicological standpoint. Both men are

> seeing great success with their patients.

>

>

>

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> What does he use to treat mold illness?

> Bobbie

Re: [] markinvoch

> Angelika:

> Does Dr. Marinkovich have a website? If so please share.

> I don't have plans to fly to CA and consult with him; would be interested to

> learn more of his protocols.

> Thanks so much,

> Rosie

Hello Bobbie and Rosie,

Marinkovich is individualized. Not a " catch all " protocols. I don't know what he

would prescribe for you but this is my plan:

Firstly --remove myself from the mold - this is 99% of the recovery. Avoidance

is crucial. The rest of it... the immune system needs help.... I was put on a

very restrictive diet which can be found here.

http://www.mold-survivor.com/dietcopyright.htm I stick to this religiously.

Then I was put in anti-fungals.

Killing mold is not like taking antibiotics for two weeks. Mold is programmed to

decompose things and has a damn strong survival rate. Thus mold / fungal

treatment must be done steadily, consitantly and over a long period of time.

Avoidance is key though - no amount of drugs or diet is going to help without

first getting away from this killer. I still have reactions due to being

over-sensitized and am now MCS. But that will decrease over time. I have gotten

far better in the last six months. In fact six months ago - I there was no way

in hell I could have gotten my thoughts together enough to write an email like

this one ! I am sure Dr. Marinkovish would welcome a call from you. His staff

is nice.

Dr. Shoemaker is another top-notch " best of the best " expert in the field. I

have not gone to him but people on this list can tell you more about him. He is

located back east and may be closer to you.

Please keep in mind not everyone is the same, not every doctor uses the " exact "

same approach and what works from one person may not for a another. But most of

the doctors discussed on this list are experts, are wonderful and have results

in helping thousands of people.

Marinkovich contact:

Marinkovich

801 Brewster Ave #220

Redwood City, CA 94063

650-482-2800

Dr. Shoemaker's website is:

http://www.chronicneurotoxins.com/

I hope this helps.

Keep going ! We're all in this together.

Avoidance is key - get away from this stuff immediately !!! Mold kills.

Angelika

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

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Hi Angelika:

Thank you so much for your detailed summary of Dr. Marinkovich's protocols.

I'm always curious about different protocols and what the experts are

prescribing for obvious reasons.

I also am doing much better than I did originally and am able to function

almost normally when not exposed. As you, I developed MCS as well in

addition to my original Lupus. lol I was laughing yesterday when I had to

climb onto our roof to check on the roofer 3 times thinking of and his

mountain climbing. Decided I was climbing mountains also on my roof top

since it's multi-level and had to do some jumping from one point to another.

Early on I put myself on the mold-diet or should I say my version of the

mold diet that still restricts the food I needed to avoid for my Lupus. The

only thing I eat which is not on the mold-diet are organic eggs. I will

make that another post.

Was just hoping Marinkovich might have a web site to increase my knowledge

and view his protocols and thoughts on this subject.

I'm so pleased you are doing better. And I totally concur we must restrict

our diet and avoid mold and other chemical toxins to which we are reactive.

I was so ill originally even the mold on a lemon or in the produce section

of a grocery store would cause a reaction. I believe in prevention and will

use a charcoal face mask when I'm in a possible moldy or other environment

to which I react, still watch my diet, cook everything from scratch, eat

nothing prepared or outside the home, and am always checking my home for any

water leaks to prevent further damage.

And yes you are so correct that we are all individuals and each treatment

must be custom to our di-stress not a one size fits all. We also change

with exposures, stress and other factors and our protocols need to be

changed also.

Thanks again and so delighted you are doing better,

Rosie

> Marinkovich is individualized. Not a " catch all " protocols. I don't know

> what he would prescribe for you but this is my plan:

>

> Firstly --remove myself from the mold - this is 99% of the recovery.

> Avoidance is crucial. The rest of it... the immune system needs help.... I

> was put on a very restrictive diet which can be found here.

> http://www.mold-survivor.com/dietcopyright.htm I stick to this

> religiously. Then I was put in anti-fungals.

>

> Killing mold is not like taking antibiotics for two weeks. Mold is

> programmed to decompose things and has a damn strong survival rate. Thus

> mold / fungal treatment must be done steadily, consitantly and over a long

> period of time. Avoidance is key though - no amount of drugs or diet is

> going to help without first getting away from this killer. I still have

> reactions due to being over-sensitized and am now MCS. But that will

> decrease over time. I have gotten far better in the last six months. In

> fact six months ago - I there was no way in hell I could have gotten my

> thoughts together enough to write an email like this one ! I am sure Dr.

> Marinkovish would welcome a call from you. His staff is nice.

>

> Dr. Shoemaker is another top-notch " best of the best " expert in the field.

> I have not gone to him but people on this list can tell you more about

> him. He is located back east and may be closer to you.

>

> Please keep in mind not everyone is the same, not every doctor uses the

> " exact " same approach and what works from one person may not for a

> another. But most of the doctors discussed on this list are experts, are

> wonderful and have results in helping thousands of people.

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Thank you for the information. I am a Shoemaker patient. Just finished my

Procrit

injections, am in a " bubble " for a time, and taking Cholestyramine. For the

first time in

many years my CFS and Fibro s/s are almost gone. Sleep and water retention (MSH

is low)

remain an issue. I even walked 3 miles several times the last few weeks. Best

of all I am

focusing on and retaining new information! My fog is gone. I am very excited

about it all

and want to learn everything that I can about the biotoxic illness world.

Bobbie

--- In , " Angelika \(mold list\) " <moldhelp@p...>

wrote:

>

> > What does he use to treat mold illness?

> > Bobbie

> Re: [] markinvoch

> > Angelika:

> > Does Dr. Marinkovich have a website? If so please share.

> > I don't have plans to fly to CA and consult with him; would be interested to

> > learn more of his protocols.

> > Thanks so much,

> > Rosie

>

>

>

> Hello Bobbie and Rosie,

>

> Marinkovich is individualized. Not a " catch all " protocols. I don't know what

he would

prescribe for you but this is my plan:

>

> Firstly --remove myself from the mold - this is 99% of the recovery. Avoidance

is

crucial. The rest of it... the immune system needs help.... I was put on a very

restrictive

diet which can be found here. http://www.mold-survivor.com/dietcopyright.htm I

stick to

this religiously. Then I was put in anti-fungals.

>

> Killing mold is not like taking antibiotics for two weeks. Mold is programmed

to

decompose things and has a damn strong survival rate. Thus mold / fungal

treatment

must be done steadily, consitantly and over a long period of time. Avoidance is

key though

- no amount of drugs or diet is going to help without first getting away from

this killer. I

still have reactions due to being over-sensitized and am now MCS. But that will

decrease

over time. I have gotten far better in the last six months. In fact six months

ago - I there

was no way in hell I could have gotten my thoughts together enough to write an

email like

this one ! I am sure Dr. Marinkovish would welcome a call from you. His staff

is nice.

>

> Dr. Shoemaker is another top-notch " best of the best " expert in the field. I

have not

gone to him but people on this list can tell you more about him. He is located

back east

and may be closer to you.

>

> Please keep in mind not everyone is the same, not every doctor uses the

" exact " same

approach and what works from one person may not for a another. But most of the

doctors

discussed on this list are experts, are wonderful and have results in helping

thousands of

people.

>

> Marinkovich contact:

> Marinkovich

> 801 Brewster Ave #220

> Redwood City, CA 94063

> 650-482-2800

>

> Dr. Shoemaker's website is:

> http://www.chronicneurotoxins.com/

>

>

> I hope this helps.

> Keep going ! We're all in this together.

>

> Avoidance is key - get away from this stuff immediately !!! Mold kills.

> Angelika

>

>

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

>

>

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Bobbie - How long did you do the procrit? (I'm in a fight with my insurance

company over this one medication. Thought I'd like to know just how much money

we're really arguing about.)

Bobbie Delory <realmoldygal@...> wrote:Thank you for the information. I

am a Shoemaker patient. Just finished my Procrit

injections, am in a " bubble " for a time, and taking Cholestyramine. For the

first time in

many years my CFS and Fibro s/s are almost gone. Sleep and water retention (MSH

is low)

remain an issue. I even walked 3 miles several times the last few weeks. Best

of all I am

focusing on and retaining new information! My fog is gone. I am very excited

about it all

and want to learn everything that I can about the biotoxic illness world.

Serena

www.freeboards.net/index.php?mforum=sickgovernmentb

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

Music Unlimited - Access over 1 million songs. Try it free.

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Serena,

I did the Procrit for 21/2 weeks. Do you have a copy of the protocol? I have a

great med

plan so 13 vials cost me $75.00. Do you see Shoemaker? I think he charges for

the visit

when you get the injection, he has it in the office.

Bobbie

Thank you for the information. I am a

Shoemaker patient. Just finished my Procrit

> injections, am in a " bubble " for a time, and taking Cholestyramine. For the

first time in

> many years my CFS and Fibro s/s are almost gone. Sleep and water retention

(MSH is

low)

> remain an issue. I even walked 3 miles several times the last few weeks.

Best of all I am

> focusing on and retaining new information! My fog is gone. I am very excited

about it

all

> and want to learn everything that I can about the biotoxic illness world.

>

>

>

>

> Serena

> www.freeboards.net/index.php?mforum=sickgovernmentb

>

>

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

> Music Unlimited - Access over 1 million songs. Try it free.

>

>

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Last I saw, there is no single copy of the protocol(s). And even if there were,

I wouldn't put out it out on a public board. It's individualized stuff that

should not be done outside a physician's care.

But yes, I'm one of Shoemaker's patients. Since I live out of his area, we

wouldn't be doing it at his office. (Wouldn't be the first time I had an

injectable prescription, so I'm fine with that.) This is the first and only time

my insurance has fought me on anything. The fools tried to tell me that

off-label prescribing is flatly illegal. When I suggested to them that off-label

drug use would have virtually every physician in the country up on charges by

morning if that were true, they just insisted all the more. Doh! And me without

my boots.

I'm glad to hear that the procrit seems to be effective for you despite the low

MSH. I was trying to figure whether to go ahead and wait it out, or just bear

the expense up front and let the chips fall where they may. More on our

wonderful friends in the insurance industry in a sec...

Serena

www.freeboards.net/index.php?mforum=sickgovernmentb

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

Music Unlimited - Access over 1 million songs. Try it free.

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What is procrit?

On Sun, 9 Oct 2005, Bobbie Delory wrote:

> Date: Sun, 09 Oct 2005 02:12:58 -0000

> From: Bobbie Delory <realmoldygal@...>

> Reply-

>

> Subject: [] Re: markinvoch

>

> Serena,

>

> I did the Procrit for 21/2 weeks. Do you have a copy of the protocol? I have

a great med

> plan so 13 vials cost me $75.00. Do you see Shoemaker? I think he charges

for the visit

> when you get the injection, he has it in the office.

>

> Bobbie

> Thank you for the information. I am

a

> Shoemaker patient. Just finished my Procrit

>> injections, am in a " bubble " for a time, and taking Cholestyramine. For the

first time in

>> many years my CFS and Fibro s/s are almost gone. Sleep and water retention

(MSH is

> low)

>> remain an issue. I even walked 3 miles several times the last few weeks.

Best of all I am

>> focusing on and retaining new information! My fog is gone. I am very

excited about it

> all

>> and want to learn everything that I can about the biotoxic illness world.

>>

>>

>>

>>

>> Serena

>> www.freeboards.net/index.php?mforum=sickgovernmentb

>>

>>

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

>> Music Unlimited - Access over 1 million songs. Try it free.

>>

>>

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Bobbie, just curious did Dr. Shoemaker suggest an anti-fungal diet for you

or only the Rx meds?

Rosie

> Thank you for the information. I am a Shoemaker patient. Just finished

> my Procrit

> injections, am in a " bubble " for a time, and taking Cholestyramine. For

> the first time in

> many years my CFS and Fibro s/s are almost gone. Sleep and water

> retention (MSH is low)

> remain an issue. I even walked 3 miles several times the last few weeks.

> Best of all I am

> focusing on and retaining new information! My fog is gone. I am very

> excited about it all

> and want to learn everything that I can about the biotoxic illness world.

>

> Bobbie

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It is a drug that is often used to treat people with anemia or cancer.

Bobbie

Thank you for the information. I

am a

> > Shoemaker patient. Just finished my Procrit

> >> injections, am in a " bubble " for a time, and taking Cholestyramine. For

the first time

in

> >> many years my CFS and Fibro s/s are almost gone. Sleep and water retention

(MSH

is

> > low)

> >> remain an issue. I even walked 3 miles several times the last few weeks.

Best of all I

am

> >> focusing on and retaining new information! My fog is gone. I am very

excited about

it

> > all

> >> and want to learn everything that I can about the biotoxic illness world.

> >>

> >>

> >>

> >>

> >> Serena

> >> www.freeboards.net/index.php?mforum=sickgovernmentb

> >>

> >>

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

> >> Music Unlimited - Access over 1 million songs. Try it free.

> >>

> >>

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In my brain fog during treatment I cannot recall an antifungal diet. He does

however use

the drug Actos for which he puts you on a low amylase/low glycemic index food

diet.

Bobbie

--- In , " Healthier4All " <Healthier4All@h...>

wrote:

>

> Bobbie, just curious did Dr. Shoemaker suggest an anti-fungal diet for you

> or only the Rx meds?

>

> Rosie

>

>

> > Thank you for the information. I am a Shoemaker patient. Just finished

> > my Procrit

> > injections, am in a " bubble " for a time, and taking Cholestyramine. For

> > the first time in

> > many years my CFS and Fibro s/s are almost gone. Sleep and water

> > retention (MSH is low)

> > remain an issue. I even walked 3 miles several times the last few weeks.

> > Best of all I am

> > focusing on and retaining new information! My fog is gone. I am very

> > excited about it all

> > and want to learn everything that I can about the biotoxic illness world.

> >

> > Bobbie

>

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Re: [] markinvoch

> Hi Angelika:

>

> Thank you so much for your detailed summary of Dr. Marinkovich's

protocols.

> I was so ill originally even the mold on a lemon or in the produce section

> of a grocery store would cause a reaction.

And here I thought I was the only one that reacted to a bit of mold on a

lemon in the grocery store.

Good Lord, I remember it clearly still ...walking through the isle and

suddenly my legs went out from under me.

My lungs seized up and as I got up I realized that I was standing next to

the lemon's and lime and a few of them had a bit of white fuzz on them. Took

me three days to recover. *%( & (@ & %)!@ I went home and cried thinking I could

never go outside again. Thankfully, it's not that bad anymore.

Angelika

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> And here I thought I was the only one that reacted to a bit of mold on a

> lemon in the grocery store.

> Good Lord, I remember it clearly still ...walking through the isle and

> suddenly my legs went out from under me.

> My lungs seized up and as I got up I realized that I was standing next to

> the lemon's and lime and a few of them had a bit of white fuzz on them.

> Took

> me three days to recover. *%( & (@ & %)!@ I went home and cried thinking I

> could

> never go outside again. Thankfully, it's not that bad anymore.

>

> Angelika

>

Huggies Angelika--you are another " me " . Thank you for sharing this. I

remember walking into my organic produce co-op and having a severe reaction;

coughing, throat tightening on me, chest felt like I was being squeezed,

legs got weak, foggy brain. Seems a moldy potato (and the older ones not

stored properly will be very moldy) caused my reaction. Had to leave

without my produce and drive home very carefully and yes I was ill for

several days, couldn't sleep due to pain.

I'm much better now. Yesterday visited my very favorite wholesale herb

nursery in the country. For the last few years couldn't go there because

many of their buildings/greenhouses covered with mold and I'd react.

Decided I needed some plants for my Fall garden, am way past my planting

deadline due to having spent much of my Summer with water leaks, tornado and

hurricane. I was hesitant. Did take with me with homemade charcoal mask,

etc but decided to test first. Had no reaction whatsoever. Even their

bathroom (which I needed after drinking a few quarts of water while there,

walked through acres of fields trying to find something to wildcraft and

bring home and I did, goldenrod in bloom and fresh pine needles for tea) I

knew would be a problem and didn't quite know what to do. Since I wasn't

reacting to the mold in the greenhouses, took a risk. The bathroom's walls

2' high from ground covered with black mold. I didn't react. Talk about

doing happy dance.

lol but then I've been taking 's advise to go mountain climbing. lol in

Houston we don't have mountains but I do have a 3 story roof and had to

climb it often to make sure the roofers were actually making the needed

repairs and doing it properly. Been taking herbs for the mold and seems to

be working.

Now having said all that my MCS is still active and I will react quickly to

fabric softeners, perfumes, toiletries, still cannot go into a beauty salon

to get my hair cut. Need to figure out what I can take for the MCS to

reduce symptoms other than total avoidance.

Rosie

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HIya Rosie (and all moldies reading this thread on individual reactions)

Yep - sounds familiar. I still react though and have to be careful.

Yesterday I went house hunting; walked into a few houses and no problem.

Glory be ! I figured I could rent one of them. Then walked into the third

house for show and WHAM within minutes my knees went weak, foggy brain

started to set in. I realized it was coming from the carpeting they had laid

in the basement (moldy basement obviously). I got outta of there. The good

news is that I figured out that I cannot live in a house with carpeting and

have to have wood floors only. (Provided they weren't recently refinished.

The refinishing chems and oils do me in too.)

The MCS is in full swing. Eighteen months ago I could romp - yes ROMP -

through department stores and smell all the lovely and expensive perfumes. I

couldn't afford them but I could always scam a few samples LOL !

No more. I could wash my clothes in whatever I pleased but now can't go near

the soap isle at Target. I have to use all natural soap for clothes, body

wash, shampoo you name it or else. No nail polish remover - that kills me

for days. (BTW there's an all vegetable based nail polish remover that

causes NO reactions !) No chemical cleaning products either - only vinegar,

Borax or baking soda and dish soap from EcoVer. The local carwash knows not

to use any chems inside my car too.

Mold + chems + bad environments = serious illness for me.

Angelika

PS - I only go to the beauty shop for hair cuts first thing in the morning

before they start all the chem processing. SuperCuts usually doesn't do a

lot of dying and perming so I have found I could go there in the mornings

and I am OK. Forget the high-end places - tried that - they're loaded !

Re: [] markinvoch

>

> > And here I thought I was the only one that reacted to a bit of mold on a

> > lemon in the grocery store.

> > Good Lord, I remember it clearly still ...walking through the isle and

> > suddenly my legs went out from under me.

> > My lungs seized up and as I got up I realized that I was standing next

to

> > the lemon's and lime and a few of them had a bit of white fuzz on them.

> > Took

> > me three days to recover. *%( & (@ & %)!@ I went home and cried thinking I

> > could

> > never go outside again. Thankfully, it's not that bad anymore.

> >

> > Angelika

> >

>

> Huggies Angelika--you are another " me " . Thank you for sharing this. I

> remember walking into my organic produce co-op and having a severe

reaction;

> coughing, throat tightening on me, chest felt like I was being squeezed,

> legs got weak, foggy brain. Seems a moldy potato (and the older ones not

> stored properly will be very moldy) caused my reaction. Had to leave

> without my produce and drive home very carefully and yes I was ill for

> several days, couldn't sleep due to pain.

>

> I'm much better now. Yesterday visited my very favorite wholesale herb

> nursery in the country. For the last few years couldn't go there because

> many of their buildings/greenhouses covered with mold and I'd react.

> Decided I needed some plants for my Fall garden, am way past my planting

> deadline due to having spent much of my Summer with water leaks, tornado

and

> hurricane. I was hesitant. Did take with me with homemade charcoal mask,

> etc but decided to test first. Had no reaction whatsoever. Even their

> bathroom (which I needed after drinking a few quarts of water while there,

> walked through acres of fields trying to find something to wildcraft and

> bring home and I did, goldenrod in bloom and fresh pine needles for tea) I

> knew would be a problem and didn't quite know what to do. Since I wasn't

> reacting to the mold in the greenhouses, took a risk. The bathroom's

walls

> 2' high from ground covered with black mold. I didn't react. Talk about

> doing happy dance.

>

> lol but then I've been taking 's advise to go mountain climbing. lol

in

> Houston we don't have mountains but I do have a 3 story roof and had to

> climb it often to make sure the roofers were actually making the needed

> repairs and doing it properly. Been taking herbs for the mold and seems

to

> be working.

>

> Now having said all that my MCS is still active and I will react quickly

to

> fabric softeners, perfumes, toiletries, still cannot go into a beauty

salon

> to get my hair cut. Need to figure out what I can take for the MCS to

> reduce symptoms other than total avoidance.

>

> Rosie

>

>

>

>

> FAIR USE NOTICE:

>

>

>

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