Monday, September 7, 2015

Hydrocephalus Awareness Month

Today is the seventh day of Hydrocephalus Awareness Month and I am going to share a quote from one of my shirts I got from Hydro Angels Over America. The quote is this, You never know how strong you are until being strong is the only choice you have. I like that because sometimes people like me have to be strong. Hydrocephalus is something  that people need to know about, and it needs a cure, because it doesn't have one yet. I got this from a website on Google. I'm hoping this helps people know what others and myself have to deal with it. Hydrocephalus is a brain condition that happens when cerebrospinal fluid (CSF) — the clear, watery fluid that surrounds and cushions the brain and spinal cord — cannot drain from the brain. It then pools, causing a buildup of fluid in the skull. Hydrocephalus gets its name from the Greek words for water (hydro) and head (cephalus), and sometimes is called "water on the brain."Hydrocephalus can cause babies' and young children's heads to swell to make room for the excess fluid. Older kids, whose skull bones have matured and fused together, have painful headaches from the increased pressure in the head. If it's not treated, hydrocephalus can lead to brain damage, a loss in mental and physical abilities, and even death. With early diagnosis and timely treatment, though, most children recover successfully. Causes
When everything is working normally inside the brain, CSF flows through narrow passageways called ventricles and exits the brain through a small reservoir at the base of the brain called the cistern. CSF delivers nutrients to the brain; it also takes waste away from its sensitive areas to be absorbed into the bloodstream. If there's a blockage in any of the ventricles, CSF backs up and causes hydrocephalus. This excess of fluid in the brain also can happen when the choroid plexus (the area of the brain that produces CSF) is in overdrive or if the waste products aren't properly absorbed by the bloodstream. Congenital hydrocephalus means a baby is born with the condition. This is often due to problems like spina bifida (abnormal development of the spinal cord) or aqueductal stenosis (the narrowing of a small passageway, the "aqueduct of Sylvius," that connects two major ventricles in the brain).Acquired hydrocephalus happens after birth and can affect people of any age. It's usually caused by bleeding in the brain. This can happen in premature babies or people who've had traumatic head injuries. Some kids can develop hydrocephalus due to a tumor or infection in the brain. Some cases have no known cause. Signs in Babies Symptoms of hydrocephalus vary depending on the age of a child. Babies under the age of 1 year will have heads that appear very swollen. Their skull bones — thin, bony plates that have not yet fused together — are connected by fibrous tissue called sutures. These sutures, or "soft spots," have not yet hardened and therefore stretch and expand to store the excess CSF. As a result, a baby with hydrocephalus will appear to have an oddly shaped head — usually much larger than other babies the same age.
Other signs to look for include: bulging at the soft spots "split" sutures — a gap can be felt between skull bones rapid increase in head circumference swollen veins that are easily seen with the naked eye downward cast of the eyes (called "sunsetting") Depending on how severe the condition is, babies also may seem excessively sleepy, fussy, and vomit or have seizures. Young children with hydrocephalus also may miss developmental milestones or may revert to earlier developmental stages. In extreme cases, a child also may experience "failure to thrive" and miss growth milestones. Signs in Older Kids Older children will not have the easily recognizable symptom of an enlarged head because their skull bones have fused together and can't expand to make room for the excess fluid. In these cases, added pressure on the brain can cause severe headaches that may wake a child in the middle of the night or early in the morning. Kids also might have: nausea/vomiting  sleepiness
problems with balance and motor skills double vision squinting and/or other repetitive eye movements seizures Changes in personality, loss of new developmental abilities (like speaking or walking), and memory loss can happen in more advanced cases. Diagnosis A child who shows any of the signs and symptoms mentioned above should see a doctor right away. The doctor will perform examinations, which may include a medical history and diagnostic tests — like ultrasound, CT (computed tomography) scan, or MRI (magnetic resonance imaging) — to get a clear picture of the inside of the brain.

Treatment Options

It is important to treat hydrocephalus right away. Untreated hydrocephalus can get worse and cause further problems in the nervous system.
Treatment for hydrocephalus varies depending on the age of the child, the cause of the CSF buildup (whether from a blockage, overproduction of fluid, or another problem), and the child's overall health.

Ventriculostomy and Coagulation

Endoscopic third ventriculostomy (ETV) with choroid plexus coagulation (CPC) is a relatively new procedure that is becoming common for kids who need surgery. This minimally invasive approach involves placing a small, lighted camera (called an endoscope) inside the brain so that surgeons can see the surgical site on a computer monitor. Then, using very small instruments, surgeons make a tiny hole in the bottom of the third ventricle of the brain.
This creates an "evacuation route" that lets fluid drain from the brain and bypass any blockages that are causing a backup. The body then absorbs the CSF back into the bloodstream as it normally would.
After the ventriculostomy, surgeons cauterize (burn slightly) parts of the choroid plexus, the area of the brain that produces CSF. This is done to reduce the amount of CSF that the brain makes.
This surgical approach has a higher success rate than shunting (implanting a tube in the brain to drain the fluid), which used to be the standard surgery for kids with hydrocephalus. It's performed in kids ages 1 and up, but may be available to younger kids in the future.
Kids who have ventriculostomies and coagulation need to follow up with their care team often. If they develop hydrocephalus again, doctors usually have to do a shunting procedure because a repeat ventriculostomy is not likely to work. Shunt Procedure Shunt procedures, which have been done for decades, involve surgery to place one end of a catheter (flexible tube) into a ventricle of the brain and place the other end in the abdominal cavity, chambers of the heart, or space around the lungs. Fluid drains from the brain into these places and is absorbed by the bloodstream. A valve (flap that opens and closes) in the shunt system regulates the flow to prevent over-draining and under-draining.
While shunting has been an effective treatment for hydrocephalus, the long-term success rate of a shunt isn't great. There is a high chance of failure and complications after a shunt is implanted, with almost half of all shunts failing to work well within the first year. When this happens, a child needs to have surgery again to replace a catheter or valve or replace the entire shunt. Most kids who undergo shunting will require future operations over their lifetimes to deal with shunt problems.
Infections are another side effect of shunting. Most infections develop within the first few months after a shunt procedure and require temporary removal of the device while a child receives IV (given through a vein) antibiotics for up to 2 weeks. Because of the drawbacks of shunting, these procedures are done less and less these days. Doctors use shunting as an alternative when ventriculostomies and coagulation can't or don't work. Outlook With timely treatment, many kids with hydrocephalus go on to lead normal lives. Those with more complex medical problems, like spina bifida or bleeding in the brain from prematurity, may have more health problems due these conditions. In these kids, early treatment by developmental specialists, physical therapists, and occupational therapists can make recovery much more likely and greatly improve their outcomes. I can't wait to share something for day eight tomorrow, until then please enjoy these facts and the quote I have shared with you today.

Sunday, September 6, 2015

Hydrocephalus Awareness Month

Today is the sixth day of Hydrocephalus Awareness Month and today I thought I would share a Hydrocephalus Awareness Fact with you, that I found on Google. This is something that I felt was important to share with you because so many people do not understand what people like me have to go through. There are a lot more people who don't even know what Hydrocephalus is. There is not a cure for it yet, and in the photo that says there is no cure for it, it's true because the only treatment for it, is a shunt. I feel it's important to share this with all of you today because Hydrocephalus Awareness Month Matters to Me, and to the thousands of other people who are living with it.

Saturday, September 5, 2015

Hydrocephalus Awareness Month

Today is the fifth day of Hydrocephalus Awareness Month, which means instead of showing you a video about Hydrocephalus and a shunt, I am going to show you a video about Hydrocephalus. Now this is a video I found on YouTube. I'm very excited to show you this video because I am hoping you'll be able to learn more about it and I hope that this will help those who don't know what Hydrocephalus is, learn more about it too. Here is the video. https://www.youtube.com/watch?v=okD6_k9Xosk This is the video that I am hoping will continue to educate people on Hydrocephalus. This month matters to me and to the people like me, going through the same things. September is Hydrocephalus Awareness Month. I can not wait to show you something different tomorrow, but until then please enjoy the video and continue to learn why it's important to know why Hydrocephalus is important and why it matters. So many people don't even know what it is. So that is why we need to help them understand what people like me are living with every single day.

Friday, September 4, 2015

Hydrocephalus Awareness Month

Today is the fourth day of Hydrocephalus Awareness Month, and I felt that it was important if I show you a video I found that talks about Hydrocephalus, and talks about a shunt. I feel that it is important to learn about the two because there are people that have absolutely no clue what a shunt is or what Hydrocephalus is, and I feel that it is not only my job to help those people learn about it this month, but our job to educate those who don't know, because there are people like me who have to live with Hydrocephalus every day and there is not a cure for it, and the only treatment for it is a shunt. I hope as I do a different post for this month, that you will learn not only what I have to go through, but what people like me have to deal with too. Here is the video that I am hoping will help those understand more and help educate them as well on Hydrocephalus and a shunt. This month matters not only to me but to the others just like me who are going through the same things. I can't wait to continue to share more this month with all of you because September is Hydrocephalus Awareness Month, and September Hydrocephalus Awareness Month Matters. I think we need to tell others about Hydrocephalus, because it's important that they know what people like me have to go through. https://www.youtube.com/watch?v=OyEoEDI_V7Q This is the video that I hope educates people more about shunts and Hydrocephalus. Tomorrow I can not wait to share something different for the fifth day, but until then please enjoy this video.

Thursday, September 3, 2015

Hydrocephalus Awareness Month

Today is the third day of Hydrocephalus Awareness Month, and I decided to show you a video that I found on YouTube of what a shunt is and what it looks like. Hydrocephalus Awareness Month Matters to me and to the thousands of other people who have it. I'm living with it every single day just like the other thousands of people like me. There isn't a cure for it yet. So here is the video.
 https://www.youtube.com/watch?v=Yb9dSjDykpI , That is the link to the video. I hope that as I do a post for this month, you will continue to learn about Hydrocephalus and why Hydrocephalus Awareness Month is important to me and people like me. I'm hoping this video helps you to learn more about what a shunt is, and how it would be hard for someone like me to describe what a shunt looks like. I was born with Hydrocephalus, and I have a learning disability. It's hard for me to make friends. I hope you enjoy the video that I am sharing with you today, because I feel it's important to tell others about what a shunt is and what it looks like, since today is the third day of Hydrocephalus Awareness Month. I am going to be posting something different for this month, because I feel it's important not only to me, but to others who are going through the same things. This month matters.

Wednesday, September 2, 2015

Hydrocephalus Awareness Month

Today is the second day of Hydrocephalus Awareness Month and I decided that instead of a picture I would post some facts about Hydrocephalus. Now these are facts I found on Google, so these are not my own. Fact One: Hydrocephalus Also called:  water on the brain.
Fact Two: A build-up of fluid in the cavities deep within the brain.
Fact Three: Rare 20,000 to 200,000 US cases per year.
Fact Four: Medically treatable By a doctor or professional.
Fact Five: Requires a medical diagnosis Always requires lab tests or imaging.
Fact Six: Medium-term Often resolves within a few months.
Fact Seven: The extra fluid puts pressure on the brain and can cause brain damage. It's most common in infants and older adults.
Fact Eight: Hydrocephalus is characterized by head enlargement in infants. Adults and older children experience headache, impaired vision, cognitive difficulties, loss of coordination, and incontinence.
Fact Nine: Treatment is often a tube (shunt) inserted surgically into a ventricle to drain excess fluid.
Fact Ten: Ages affected: 0-2, 3-5, 6-13, 14-18, 19-40, 41-60, and 60+.
These are facts that I got off Google and now I am going to share one of my own facts. So here is Fact Eleven: Hydrocephalus doesn't have a cure. Fact Twelve: People like me are living with Hydrocephalus everyday. Fact Thirteen: A lot of people do not know what Hydrocephalus is.
So those are some of my facts on Hydrocephalus and some Google facts on Hydrocephalus.
 
 
 
 
 
 
 

 

 

Tuesday, September 1, 2015

Hydrocephalus Awareness Month

Today Is Hydrocephalus Awareness Month and I think it is important that we spread awareness by telling people who are like me what thousands of people are dealing with. The only treatment for it right now is a shunt and there is no cure for it yet. I decided that I am going to do a post for this month, so that I can tell others about what I have to go through and what thousands of other people like me have to go through. I decided that today I would post a picture of the ribbon since today is the first official day of Hydrocephalus Awareness Month and the first of September. Hydrocephalus Awareness Month Matters to me because I have it and it matters to those like me living with it too.