(It is important to know that I am not a medical doctor. I am only a mother of a boy that suffered from these. Please do not take this as medical advice, only something I came across that worked to cure my son.)
So I will assume that most of you have never heard of that mouthful of a name. I hadn’t either until June of 2011. That’s when my youngest son started developing these flesh coloured little bumps on his neck. It looks similar to the two images on this page. The best description I can think of are skin coloured moles that protrude from the skin. That doesn’t sound particularly unpleasant. However, these things multiply like rabbits. One isn’t just one, it is many more in the making. Simply put, these bumps spread through touch. Once you have the virus, you have to kill them and not touch them while you are treating them in order to make the little pests disappear.
Please know that you can catch MC anywhere. Children are particularly
susceptible because they touch a lot of things and then themselves. Also, they share clothes, painting aprons, etc.
My son caught his from his day care providers children. To be clear, I did know that her son had something on his body, but I was never told they were contagious. It could be quite a long story, but the short sto
ry is that she didn’t realize they were contagious, even though we share the same doctor, etc. She felt awful about it since her children’s disappeared quite quickly.
Suggested Cures
Our family doctor told us to let the virus run its course. No need to interfere as the Molloscum Contagiosum would disappear without treatment in two years. That made us believe it wasn’t a big deal and that they wouldn’t do much but show up as a couple bumps. WRONG! So – so very wrong. They spread and spread and spread. At this point I was getting nervous. My son had started preschool and I thought if this is happening to him, could other kids catch it?? I then started googling and I was shocked to find out how contagious they actually were and how many people suffered with large amounts of them all over their bodies for years. :(
What Impact Contracting Them Caused Our Family
My son was kicked out of preschool. They couldn’t risk other children catching it and they thought it would cause some emotional damage if they didn’t let him use certain centres and interact like the other kids did. I fully agreed. It was heart breaking for me to have to take him out. They assured me that if it disappeared, he would be welcome back.
He stayed at home with me for about a month. We did tons of things, bowling, bike rides, dog walks, children’s story time at the library, etc… but the little dude needed more from me. I contacted my older son’s school and they said they would be happy to have him. Because of the different type of interaction at the kindergarten age, he would be allowed to attend. Phew! (He has a December birthday so we had decided to wait a year, but that went out the window.)
How I Discovered A Cure
I visited my doctor again because my day care provider had told me that she would write me a note to say they weren’t contagious. When I got to the doctor, she told me that she could not write such a letter because they were in fact very contagious. (NO KIDDING!) We then told me I could try the off the shelf product for curing regular warts. She still didn’t want to use the liquid nitrogen on him (even though that was the method my day care provider had done on her son… from the same office!!) she said she didn’t want him to scar. At this point, he likely had 30 spreading all over his body. Neck, torso, legs, etc.
I was stunned. Do nothing??? Then they started up his neck and on to his face… That is when I started freaking.
I googled and googled and googled to figure out a Molloscum Contagiosum Treatment.
I found and tried:
Tea Tree Oil
Duct tape
Liquid band aids
Oil of Oregano
Acne medication
Picking them off
Hankerchiefs to hide his neck
Bandaids to keep him from touching them
I even ordered a special product to cure them online before I found this miracle cure! The package is at our house but unopened… not sure what to do with it other than bin it.
Nothing worked. It made it worse it seemed. :(
Then I asked a group of parents I have had contact with online in regards to my other son’s speech issues. Within an hour they had pointed me to what they had tried…. Get this…. Apple Cider Vinegar. Yup. That’s it.
About Molloscum Contagiosum Treatment
It sounds bananas. I know. But it works. The parents in the group shared a link to a website called Frugality is Free. The blog post is called Frugal Living: Molluscum Contagiosum Apple Cider Vinegar Treatment.
In that post, a lady shares her own son’s struggle with MC. She told her story and how she cured them. It boils down to this.
Buy copious amounts of Apple Cider Vinegar (ACV), a bag of cotton balls and a box of bandaids that are sticky, but not too sticky (we bought larger rectangular bandaids and cut them down as it begins to irritate the skin when bandaged the 7th time in seven days).
Option 1 – Pour 5 – 7 cups of ACV into a bathtub, add water and submerge your body for 30 minutes. Continue doing this daily.
Options 2 – Put cotton ball into ACV, use bandaid to put cotton ball on skin and hold there.
We did both options with my son. Both worked well. I do believe that the bandage route is likely more effective, but it just irritates the skin so much that you will have to eventually give your skin a break or risk getting an infection from raw skin.
It is also important during the treatment process that you change your clothes each day/night and never reuse a towel. The virus can stay on these items and you don’t want that. In fact, if you have them on your face or neck, you will want to change your pillow case daily too.
The bumps will become larger, likely redder and then develop a white looking pit, similar to a pimple. I have heard of some people removing the white stem and some people simply leave it. Our son said it hurt when we tried to remove them, so we only tried when they were almost falling out, directly after a bath. My husband would use a piece of toilet paper and quickly wipe at it. If it didn’t just fall out, it was left there.
Some people say their MC turned black after it was white. Our sons never really did. The white part would shrivel up and a scab would form over the MC. That’s it.
Because of the scabbing, there are going to be some marks on the body. This could turn to scarring so use Vitamin E to help with that. Also, some people used polysporin (or something similar) to help with the scabbing or if the bumps were irritated from the ACV or bandages.
Some people said they cured in two weeks. Others it takes longer. I think the difference is how many you had to start with. As well, people with a lower immune system will have to use the treatment for longer as their body is not as healthy and not as able to attack the MC like a healthy body.
Are They Cured?
Aaaaalmost. He has four active bumps that we are still treating. Two on his neck, one on his arm and one on his foot. We began treating them on December 15th and have watched his 50+ bumps disappear down to four!!!! I am guessing that within the week he will be MC free. Of course we need to keep watch on him to make sure no others crop up, as well the rest of the family needs to keep watch. But I’m confident we have kicked the ass of Molluscum Contagiousum.
I needed to share this info because it is shameful how none of the medical professionals are aware of such a simple cure. Even when I showed my doctor what was happening on December 20th, she responded with “You think that’s working” and proceeded to prescribe an acid that I was to apply at home and would burn them off. No thanks little lady… I’ll look after my kids on my own like I always have.
Other Tid-Bits
- One person I spoke to thought that MC was a sexually contracted disease. This is false. Although it can obviously be transferred during sex if there are uncovered bumps and they touch the other person, but this IS NOT a sexually transmitted disease.
- They can grow anywhere on the body, except for the palms of hands the soles of feet.
Just a blog post about our experience using the CitiKitty. I learned about it on Shark Tank and decided the minute I heard the owner giving her account, that we needed to get one for our cats.
Our oldest son was recently diagnosed as having a form of Apraxia. There are a few different names for this, but for simplicity’s sake, I’m going to refer to it as Oral Apraxia.