« January 2012 »
S M T W T F S
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30 31
You are not logged in. Log in
Entries by Topic
All topics  «
Road to Survival
Blog Tools
Edit your Blog
Build a Blog
RSS Feed
View Profile
The Road Before & After Surgery
January 26, 2012
A Productive Head Day!
Mood:  amorous
Now Playing: Day 650-The Final Road To Survival

Drano day TAKE 3 and...ACTION!

It seems I just can't get on any type of schedule now with my treatments. Today I have been dealing with the overwhelming back of head pressure that comes in waves. Its also making me extremely irritable so I thought it would be a good idea that my friend does his own thing today and I do mine. The vomiting accompanies the waves of pressure then I finally get some relief. A few hours later I am right back at it again. Gees!

At least I have found a way on my own to finish the rest of the furniture re-staining project. This way I have the entire upstairs bedroom to lock myself in from the rest of the world. It was also nice to escape the confinements of the ole couchbed and television. There was still three pieces of furniture left to stain and polish. I took my time and spent all day completing everything. It felt great to be productive again regardless if I had to take numerous bathroom breaks to get sick. The furniture looks almost brand new again! The wood was pretty dry so the dark stain took quickly. Between the new comforter set and the beautiful newly polished furniture it looks good enough to sleep in the bedroom again! Sounds like a great idea but the last time I was able to sleep in a bed without getting sick was over four years ago. I must now sleep elevated on a firm surface thus having my ole couchbed.

Yes. GP suks!

I had to call for some backup due to all the monsoon rain we are having once again. The temperatures are also back to feeling more like spring which has everyone getting sick with upper head and respiratory infections. My basement wall is leaking again due to all of this darn rain. I can't drive to go buy some caulking to seal the leaks before they got worse so I had to call for some help. Thank goodness for assistance! If you see me near the coastline soon no worries...I might just float down there in my house, hahahaha! Yes. That is how bad the rain is becoming and destroying any grass that any one has left in their yard. Pumpkin kitty had to go back to the veterinarian due to his respiratory infection is still lingering. The rest of the fur kids are 100% better so the veterinarian is just hoping it doesn't rebound and they all pass it around again. UGGGG! Poor Pumpkin. In between sneezing constantly he just lays around and sleeps a lot. At least they were able to give him another injection of antibiotics then we have to give him another round of medication for the next several days. Hopefully this time it will do the trick!

Well off to put the dressers back together again and give them one final polish! Jersey Shore is on tonight so better get my poof and head back to the ole couchbed. CHEERS!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: January 27, 2012 4:12 AM EST
Post Comment | Permalink
January 25, 2012
Things That Make You Say...Hmmmm?...
Mood:  chillin'
Now Playing: Day 649-The Final Road To Survival

As I lay here once again on the ole couchbed surrounded by my water, Slimfast and other tasty GP liquid diet yummy drinks (being sarcastic) I question what the heck came over some of these parents on a few of these reality television shows?...

Let's start off first with "Dance Moms." One would think these kids were playing lead role in a Broadway show! One would also think these Moms need to maybe get a life that doesn't evolve around putting their girls in the presence of some menopausal woman belittling them. WHEW! Have you watched this train accident waiting to happen as each competition makes those watching literally lose the rest of their hair? The woman who owns this dance studio makes any horror movie look 'G' rated. If I had someone who taught me dance put me down and then in turn have a few cursing matches with my own parent then I can only imagine at their age what they have to look forward to when they get older. Just a shame they allow such a show and its a slap in the face to such young talent. When the woman states she is looking for a husband instead of gifts that the parents and children buy her I wonder what type of gentlemen would want to be critiqued the rest of their lives? A few episodes was enough for me to say, "NEXT!" PS: I cringe at anyone who names their child, "Abby Lee."

Mind you this is what happens when you are stuck home recovering from a brain injury and there isn't a darn thing on even with over 300 channels. I just realized by my friend that we have over 400 channels. OOPS! Regardless this is why I have become the channel surfer because there isn't anything on besides HGTV and CNN. Huge Anderson Cooper fan!

Me and my friend just finished watching the most hilarious show of them all which is bad television at its finest! "Toddlers and Tiaras." Reality isn't really reality anymore. Its more like scripted television where the producers decide once the tape is cut in the editing room just how they will present you to the rest of the viewing world. Nothing quite like watching parents live their dreams out through hair clip ons, false eyelashes, flipper-fake teeth, spray on tans and enough Aqua Net that if someone lit a match we would all blow up! Hahahaha! I remember way back in the day when beauty pageants didn't involve parents standing behind the judges motioning each move their child should make. I tend to think anyone who has a video recorder at these glitz beauty pageants also must hold a top rated U Tube video channel. I get more of a kick watching the parents who act like maybe they need to be in the 2-6 year old group instead of the actual child. Hahahaha!

The best part is when the child doesn't hold up to their parents expectations and walk away with the average $500-$1,000 top prize, although mind you it costs almost the same amount just to enter into these pageants. I think maybe they need to give the parents a Monster energy drink and a dozen of pixie sticks first before announcing the grand supreme prize winners. Surely it would make for the best television of all! Hahahaha! Come on? Making a child lose weight when they are only 8 years old or how about only having children for the sake of putting them into beauty pageants? I think some these parents should had instead invested into Mattel and build a Barbie house and bought a Barbie corvette and then hit the road aka solo. Its sad to imagine the consequences and self esteem issues these children will grow up having from being forced into a distorted pageant world by their parents living their lives through them. Sure isn't what it used to be back in the day but boy! is it extremely fun guilty pleasure watching these parents behave like children!

On a more productive note...My friend started re-staining furniture in the spare bedroom. The furniture was handed down to me and the last time it had a good refinishing was years ago. I did my best to help assist with polishing the parts that were eye level. Anything besides watching television is a blessing! Amen. We also baked some cupcakes. I never was too much into cake or cupcakes. I always preferred the icing. It takes a lot of sugar anymore to keep my levels up. Same goes for staying hydrated increasing my fluids due to low blood pressure associated with my Gastroparesis. At least I can say I am getting better at monitoring both and that's a good thing!

Drano day didn't happen today. I am way overdue but each treatment must be considered very carefully. If I am experiencing excessive head pressure or vomiting as well if my blood pressure is running too low treatment must be held off for another day. My doctors leave the decision in my hands now because they feel I know my body best and don't want to jeopardize pushing me into a treatment on a day when I am not doing well to begin with. Just part of living a Gastroparesis life.

I will be coming up on two weeks soon healing from the concussion. Its a slow process but in order for it to be a successful one without suffering any further complications I need to keep remembering one word. PATIENCE.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: January 26, 2012 3:42 AM EST
Post Comment | Permalink
January 24, 2012
Darn GP!
Mood:  lazy
Now Playing: Day 648-The Final Road To Survival

So...Looks like this won't be a Drano gal for this gal. I am not having a good head day nor blood pressure day either. Darn GP! No wonder I can't ever plan things out because when you live with Gastroparesis things are always changing.

I had my Hell-In-A-Jug ready as well my Hawaiian punch chaser to start the treatment around 3:30pm. After doing a touch more walking and things around the house than compared to yesterday it all went downhill from there. My head started pounding then the horrible pressure began to work from the right side of my head through my ears then down to my neck. Next of course is motion sickness then vomiting. When I attempted to take a shower later this evening I got quite dizzy so it was a quick one then back to my ole couchbed to rest with ice packs. With my blood pressure running low I made a smart decision not to do treatment today because it does cause cardiac side affects. Its not a safe idea right now so unfortunately Drano has to wait.

There are a few house projects that need to be done around the house. So far my friend has been doing most of them. Of course I am limited due to the concussion so its been very frustrating to say the least! Let's just say I am NOT liking all the restrictions I now have in my life but just praying recovery is sooner than eight weeks before I go nuts! Hahahaha! I do have my wheelchair at home so maybe my specialist will allow me to at least go out to the mall or somewhere close to my home by next weekend just to get a change of scenery. I know...It's called patience and I am quickly running out. Some would say I would make a great contestant on the show 'Big Brother!' Me stuck in a house? No problem! I could win it seeing isn't that what I have been doing already most of my Gastroparesis life? Amen.

A friend of mine who doesn't have Gastroparesis but another chronic condition mentioned to me how hard it is dating and finding a companion. They said, "Why don't they have a dating site for those who are disabled? A way to connect with those of the opposite sex who also suffer from a disability?" Hmmmm....I honestly thought that was a very good point and a great idea too! Its hard dating when you get older but add a chronic or terminal condition to the mix? Forget it! Seems you have to hide whats going on internally especially if you can disguise it externally. Marriage isn't what it used to be years ago. I believe when you take those vows and sign that marriage certificate and its says, "Till death do us part" that it be taken seriously and there is no getting out of the marriage. Instead you have to work through your problems and differences.  I don't believe in divorce however I find myself in that exact position. I believe if there is a problem by golly it can be fixed. Sadly its when one spouse fails to work together and communicate is when they also fail the marriage. I don't believe in anyone who says it was both parties fault that the marriage ended. That isn't the case because there is always that one person who doesn't want to work on keeping their vows. Do I believe in spousal support? Yes I do unless both parties make equal in salary. If not then the lesser spouse should be granted temporary financial support. I guess I needed to be born in the 30's or 40's when there was rarely such a thing heard of as a divorce. Now marriage comes with a 50% divorce rate so some how, somewhere, something went way wrong.

Maybe we do need a dating site to connect those like us who are looking for someone special who don't discriminate based off of a medical condition but instead can see the person for who they truly are. Maybe I need to start playing the lottery again. I think my friend has a great potential business avenue to look into! Until then my dear friend never lose hope because there is someone for everyone out there who will never let you down and never give up and will see you for the beautiful person you truly are. Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: January 25, 2012 2:54 AM EST
Post Comment | Permalink
January 23, 2012
B O R E D.
Mood:  down
Now Playing: Day 647-The Final Road To Survival

Boy! OH Boy! Am I B O R E D!

It's now been officially a week since I got my concussion and I am going nuts being stuck at home! I am also going nuts with all this resting on my couchbed. I am shocked that the number pad on my satellite dish remote haven't come off yet from all the channel surfing! Hahahaha! Once I get up to walk around every other hour I am finding myself looking for anything to do. Anything at all even if it is or isn't productive. Just anything besides watching television. I lost track how many times I have walked around the house today saying, " I am BORED!" I tend to think I am also driving my friend nuts and sure bet they were glad to go to work today! Hahahaha!

Since I lost more weight over the past six months I ended up finding over six pairs of winter jeans and pants as well sweaters to donate to the local Goodwill store. Now that I wear a size 1 or 2 depending on the designer and size XS in tops most of my clothes no longer fit. I can only imagine once I go through my spring and summer clothes but those can wait seeing I am NOT looking forward to the upcoming months. I am still crossing my fingers we get hit with lots of snow in February. WHOAHOA!

Oreo is doing about the same. He still has seizures and I do my best making sure he is safe and comfortable. That is the nice part about being home with a sick fur kid. I can't see me being anywhere else knowing he might have a seizure and no one was there for him. Cuddles kitty is still waiting for someone to come home that officially moved the rest of their belongings out this past weekend. I feel horrible for the fur kids because 13 years is such a long time to be used to the same faces around the house. Me and my friend have been doing our best to help them readjust to the changes but its still been tough. I remember this same person telling me a few years ago that those who walk away and leave someone who is sick is a weak person. Now I question if they realized when the going got tough they too also got going?.. Sadly they are not the only ones in my life who have done the recent disappearing act. The words: "Abandoned" and "Neglected" seem to fit. Some question how anyone can leave someone who clearly needs help and how their guilt and subconscious don't eat them alive or at night when they sleep?.. I now find myself with all my guards up with little trust and faith in anyone within the area. Rightfully so because I refuse to get hurt again. I have been questioning whether its a good idea to remain in this city due to all the negativity and bad memories that lurk around me. My parents live here and honestly that is pretty much the only thing that keeps me grounded. I do have a handful of very loyal, loving and compassionate friends who always accepted me for me whether I am normal or sick. My friend suggested this afternoon that once I make a full recovery from the concussion that we go out with a few of his friends. It was a great idea but I told him I don't trust anyone around here and don't feel comfortable meeting anyone new. If I moved to a different state I could at least have a fresh start on a clean slate. I could be me without being judged. I would also keep my medical condition hidden behind physician doors or online.

Sometimes I just wish I was me again without Gastroparesis. For such a poorly understood GI disorder that fails to get the much needed research money from federal grants it can sure leave behind a very destructive path physically and emotionally. Amen.

Today I had to cancel all of my upcoming doctors and dentist appointments for the remainder of the month and into early February. I do have to see my doctor who is closely monitoring my recovery from the concussion. Luckily his office is just a mile from my home. I will be seeing him late next week to see where I am with the post concussion syndrome. I told him that the depression has been horrific the past three days! I have never been depressed nor a depressed person. I am the type of individual who also doesn't do pity parties but it seems when you suffer from a concussion depression can be part of the symptoms. Depression he said is very common and something we need to also keep a very close eye on because it can continue even after recovery. They can't really put me on anything for depression seeing its not a chemical imbalance problem but part of the brain trauma from the concussion. Same goes for the vomiting, nausea, irritability, memory problems, brain fog and feeling all over the place. 8 weeks seems to be reasonable since I already had prior neuro problems due to my seizures.

February can't get here soon enough so I can say "BYE BYE" to this hellish first month of the year. Once I fully recover I can't wait to just take one night out on the town, even if only for a few hours. AMEN! I tried to talk my way around maybe taking a 'small' car ride if my friend drove however my doctor quickly shot that idea down as well the hospital physicians. Heck, it was worth a try! Need any sewing done? I might be your gal! Need any taxes done? I might be your gal but I can't promise they will be done right and Uncle Sam won't be knocking at your door later this year. Hahahaha! Just blame it on the head gal! Me!

Well back to channel surfing and speaking of water...Its Hell-In-A-Jug day tomorrow. WHOAHOA! I tell ya! The things this gal has to look forward to now huh?! CHEERS!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: January 24, 2012 3:15 AM EST
Post Comment | Permalink
January 22, 2012
3rd Time Is A Charm!
Mood:  down
Now Playing: Day 646-The Final Road To Survival

I guess even when your sick as heck the 3rd time can always be the charm!

Same goes for visiting the local hospital emergency department. This is now the third time in less than a week I have been in the hospital. All because I failed (Yes! I take full responsibility and blame) and forgot to check my blood pressure and blood sugar as well got up way too quickly from my couchbed, lost my balance, hit a wooden side table at the same time Oreo's 50 pound body and skull jumping mid air then blacked out. This obviously all led to my concussion and nose issues. Now I am still royally paying for it all because I was dumb that day and forgot I was sick. Maybe I was too busy dreaming about a vacation in Hawaii then when I woke up I might had 'forgotten' I have Idiopathic Gastroparesis?...Regardless the excuses I find for my lack-of responsibility watching my health closely this concussion is getting very serious.

This weather is still confused so unfortunately the trip to the hospital was an icy one. I was WIDE AWAKE seeing I don't need to fall on the ice.  I was also very concerned with my friend driving me to the hospital working on more than 24 hours without sleep. It was a very scary ride to the emergency room but we both made it. WHEW! I only had to sign in seeing my doctor called ahead of time and they already had me in their computer system. We waited maybe five minutes before they took me back to a room. Luckily the first emergency room doctor was working and she came in to exam and talk to me. She completely agreed the concern with feeling worse and having the extreme head pressure with vomiting. Obviously something is going on and my doctor placed an order of tests to be run including a cat scan. Instead of taking a few steps forward the emergency room doctor explained I took about twice that in steps back. My blood pressure was too low for starters and even after almost two large iv fluid bags I was still running a bit low. The vertigo and head pressure is from the concussion. Although I thought maybe I took a little hit I guess I took a huge hit. After the test reports came back the doctor came in to tell us the news and next game plan.

It will now take anywhere from 6-8 weeks for my brain to fully recover as well I am experiencing terrible post concussion syndrome. The vomiting is from the head pressure which isn't helping matters leaving me dehydrated and making my Gastroparesis go all over the place. I also feel emotionally all over the place and starting to experience depression. I am finding myself the past four days crying more now than I have my entire lifetime. Drop a pin and I will lose it. At least I know this is all still part of my brain trying to recover. I am thankful my doctors are monitoring things very closely and especially when it comes to depression. Its going to be hard because I am used to keeping active around the house even during treatments but now I am stuck on my couchbed most of the day. This isn't going to be a good month nor is February.

S I G H...

My friend luckily caught up on a few zzzz's while waiting in the hospital room. They made sure to put me in a room far away from other patients who had the flu or other viruses because I don't need anything else right now on my full plate. I won't be knocking or falling on any wood right now either! Hahahaha! Funny now but it sure wasn't a week ago. After the final tests came back and the iv treatments were finished the doctor came back in to go over post concussion home care. They don't want me out jeopardizing myself by falling or getting another concussion that could end up being fatal. Especially with my low sugar and blood pressure problems. Its important I get lots of rest but I still need to get up every other hour and do my best to walk around. I am on a precautionary antibiotic as well decongestant since I will be laying around a lot. They have me on two anti vomiting and nausea medications and changed my medicine for the head pressure. All of course cause drowsiness but if that means no scary tree or dragon nightmares then I am alllllllll for it! Hahahaha!

So what did I do all day? GUESS! Couchbed, TV, walk around, take in fluids then back to my couchbed. Couchbed, TV, walk around, take in fluids then back to my couchbed, etc, etc, etc. You get the point...BOY OH BOY! Am I already BORED AS HECK! I guess like my own doctors and hospital physicians said, "Its going to be rough but you must be patience in order to make a full recovery."

This is going to be one hellish recover and I already have treatment again in two day. GEES!


Posted by GastroparesisAwarenessCampaignOrg. at 11:09 PM EST
Updated: January 23, 2012 12:05 AM EST
Post Comment | Permalink
January 21, 2012
Predict The Unpredictable...
Mood:  down
Now Playing: Day 645-The Final Road To Survival

When you live with Gastroparesis there will always be two things for certain which are:

  1. Expect the unexpected
  2. Predict the unpredictable.

I am still trying to finish up part of my last treatment just in time for another treatment come Tuesday. Honestly I don't even know how I keep up with this crazy schedule. Doing it with a brain injury...Forget it!

I still feel horrible. I can't get this darn pressure pain to ease up. If I just lay sitting up with ice or heat after an hour I seem to get a bit of relief. Once I stand up and start walking around it hits me all over again. Today I did my best to take in a little more activity finding things to do around the house. One like myself would had thought this was a good idea but to any health care professional it was a terrible idea. After being woke up at 10am then again around 12pm from those moving belongs out of the house I had to deal with some unwanted comments which ended rather quickly seeing my head and myself wasn't in the mood. By the time they made the last trip back to my house moving belongs out it was around 2pm. What a mess they left!! I was livid! The interesting part was the things they 'did' leave behind. Not like I was shocked but I am sure a few who believed otherwise might had been taken back quite a bit. It was like a huge tornado swept through the house then I just stood back shaking my head in disbelief.

GRRRR!

This started my not so good day. By 3:30pm in between taking breaks on the couch with ice and heat packs I started having severe nausea and horrible head pressure. By the time I went to call someone the vomiting started and lasted on and off for over an hour. At this point I felt extremely dizzy and my head felt like it was going to explode! I called my doctor and he quickly got back to me. He was concerned that there might be complications going on with my brain from the concussion since I shouldn't be vomiting almost a week later. He urged me to go back to the hospital so he could order some tests but stubborn me just wanted to lay back down.

Forward to 11pm this evening...As my friend finished up cleaning a huge mess from those who moved items out of the house I still wasn't feeling good and the head pressure, nausea and vomiting kept lingering. My doctor had me taking two medications that would normally stop the vomiting but it wasn't helping either. So around 11:30pm I made the decision that it would had been a good idea to listen to my doctor and go to the hospital earlier this afternoon. DUH ON ME! Now I am on my way to the hospital for the 3rd time in less than a week feeling as if once again instead of taking two steps ahead with my injury I just took another huge step behind.

What a week! What a MONTH!

As for the moving process...It is finally over although there are still things that need to be done and changed around the house but they will have to wait till another day. Its going to be a very long night into the morning hours and boy! will my friend be tired! He is going on 24 hours without sleep but illness waits for no one and I sure don't need any complications so off we go back to the hospital.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: January 22, 2012 10:05 PM EST
Post Comment | Permalink
January 20, 2012
The Strange Things That Come With A Brain Injury...
Mood:  down
Now Playing: Day 644-The Final Road To Survival

WOW! Talking about some wicked scary dreams I had last night! More like the worst and craziest nightmares ever! YIKES!

A few dear friends of mine who work in the medical field told me via text today that head injuries can cause one to have 'not so normal' dreams as the brain begins the recovery process. Just one of the many not so fun things added to my full plate. I have also been experiencing panic attacks when my head pressure gets to be overwhelming. At least I know to talk myself down from them as I tell myself, "This is normal. Breathe in and breathe out. Breathe in and breathe out...You will soon you feel better again." I came super close last night to making a phone call for someone to come over and stay till morning but being the independent gal I am I just sucked it up and worked through them. All in all let's just say I can't WAIT for my brain to fully recover. AMEN!

I had made a prior appointment a few weeks ago for Littleblue to be groomed today. My friend volunteered to take her since I can't drive nor go out right now. The new place I take her is right down the street from my house so its very close and the couple who owns it also does an amazing job! They are very good with Littleblue and Oreo. With Oreo still having seizure problems I decided to hold off a bit until later next month before he gets groomed. My friend took a photo of all the hair Littleblue left behind. This was just a touch of the undercoat she is starting to shed. The odd part is this is way too early for her to start shedding her winter coat. With all of the strange weather we are having it even has the fur gangs fur confused. She now officially looks like a huge, soft powder puff! Hahahaha!

I have now moved up to heat going along with my ice and head packs. WHOAHOA! I am determined as ever to cut the recovery time in half! I had enough of television already as well channel surfing for the rest of the year. It does help a bit more alternating between heat and ice. I can also use the heat on my shoulders and neck then the wraps with ice on my head and face. The fur kids have been enjoying time with me on my couchbed although they still need to release some of their energy so my friend takes them out for at least two walks a day.

I do my best finding things around the house to help keep me occupied. Once I get up I think, "OK. This isn't that bad now. I don't feel the pressure." This is of course within the first five minutes standing up and moving around. Ask my friend how many times I misplaced things today and he would laugh. Its the little things such as plugging in my cell phone on the charger then a few minutes later I am frantically looking around for it. I also put an open bottle of Slimfast in the cabinet then took a shower and forgot to wash out the conditioner. Hahahaha! I am hoping we can both continue laughing about things later down the road.

With my brain trying to recover things will be touch and go. I have a doctors appointment next week and a dental check up the following week. I don't want to rock the boat or more like rock the head just yet so they will both most likely need to be rescheduled. For now I just take things day by day and hour by hour. I just wish someone else could win this medical lottery of mine. I tend to agree with my friend who keeps saying, "If you are this lucky winning the medical lottery wouldn't that be great if you were just as lucky winning the real lottery?!"

Wishful thinking!

Back to channel surfing and crossing my fingers for no more nightmare dreams that involve angry trees and dragons. YIKES! Hahahaha!


Posted by GastroparesisAwarenessCampaignOrg. at 11:58 PM EST
Updated: January 21, 2012 12:55 AM EST
Post Comment | Permalink
January 19, 2012
B O R E D.
Mood:  down
Now Playing: Day 643-The Final Road To Survival

OK. So I finally got a bit of rest. I will take anything I can get however it doesn't mean that I still won't have to deal with these darn head sensations.

On top of not getting solid rest without feeling head 'funky' (I like to call it) the doorbell rings early this afternoon and then the fur kids started barking. OK. I am now officially up. GEES-Thanks FedEx! Yes, I am still not feeling well and yes, I am still irritable as allllllll heck. Not a pleasant feeling to say the least but for now I am doing the best I can.

I started a new antibiotic today since last night in the ER they did notice my lymph nodes in the back of my head were a bit swollen. I don't need any infections going on right now so better to be safe than sorry. With the weather being spring one day then winter the other its sure not helping matters. Sadly I am starting to think we will never see any significant amount of snow fall. I am taking the new combination anti inflammatory medication they prescribed for me last night but I don't really see any difference as far as relief. I honestly believe since my Gastroparesis doesn't allow for proper absorption I might just have to continue sucking it up and dealing with things as they come. Day by day. I have a few new ice packs now so its makes things much easier rotating them when one gets warm.

The fur kids are growing just as bored as I am. I lost track of how many times I said I was bored today. Funny enough my friend who always says he just wishes he had a few days to sit around and do nothing has also grown bored. Hahahaha! That makes how many of us now? Four. I better just get used to it and listen to the doctors and keep the not so brilliant ideas to myself. Like over doing it even if around the house. If I stay laying in one position with the head wraps and ice I feel a bit better but once I get up and start moving around the head pressure starts hitting me again. I can't play the Wii system or Atari with my head recovering. I can't take walks outside due to my head recovering. I can't walk on the treadmill due to my head recovery. What I can do and becoming an expect at is channel surfing! There are just way too many infomercials at night. Same with all this filler channels. At least with the living arrangements changing I got a great new package deal from Dish network this week. Now I have all three movie channels over the next three months but try watching them with subtitles and a pounding, pulsating headache. Good luck!

Maybe I just need to work on getting a list together of things I can do that don't require driving, going outside, using the treadmill, playing interactive games or bending and stooping. Hey! that would leave me with baking and channel surfing. This also requires steady balance and concentration which I don't have right now. Ask my friend who just today had to pick up skillets I dropped, a Slimfast on the floor, bird seed and the grand finale was the salt shaker that went all over me and the tile. Heck! Maybe for good luck I should had threw the rest of the salt over my shoulder instead of having him vacuum it up. Hahahaha!

Back to the ole couchbed and sleeping fur kids....


Posted by GastroparesisAwarenessCampaignOrg. at 11:40 PM EST
Updated: January 20, 2012 1:36 AM EST
Post Comment | Permalink
January 18, 2012
Jinxed January!
Mood:  don't ask
Now Playing: Day 642-The Final Road To Survival

I feel like a Zombie!

This BITES! Trust me. I enjoy being active as one can be living with Gastroparesis, even on days I am stuck in my house-jail after treatments but when that freedom is instantly taken away IT'S HORRIBLE!

I can't wait for January to be over with! 2012 seems like its been here forever and we are just starting the new year. Maybe its this jinxed city?..All I can say is this has already gotten really, really old and quick!

So much for a good nights sleep. I was awake every hour on the hour. I can't explain to you how my head felt but its a cross between feeling sandpaper, hot coals, tingling, dull and sharp pain. It starts on the right side of my face and goes around to my ear drum and back of my head. My doctors as well Urgent Care and the hospital have followed up and monitoring things very closely but today I just haven't felt too good. I actually feel worse than I did the first day. They said things will get worse before they get better but they didn't mention I won't be getting any sleep either. GRRRR....I am so irritable with the head pressure and all sorts of strange feelings that I can't stand being around myself right now. Hahahaha! I have warned those who are bold enough to come around me that right now its best I am left alone. Sound hurts and light hurts. Luckily this afternoon we finally figured out how to set the closed caption on the new television and dim the lighting down. W A Y down...

My friend said I look like a Zombie wrapped in head dressing and ice packs. There aren't enough ice packs to keep on this head. I have tried the anti inflammatory medication but haven't gotten any relief. Remember I have Gastroparesis and a paralyzed digestive system so any medication in the form of tablets or capsules doesn't work. At least I tried but for now the only bit of relief I seem to get is using over the counter Activon for the back of my neck and shoulders then ice packs for the front and back of my head. I still have bone shifted on the right side of my nose but find a bit of relief using breath right strips to help at night since its hard to breathe. Am I complaining? Oh yes! Like I said, I am beyond irritable. This reminds me of when I had viral Meningitis however my brain wasn't bruised and at least I could sleep. The head sensations are quite different too but I was also the same as now, stuck at home channel surfing for a very long time. Its a catch 22 because with my Idiopathic Gastroparesis gravity is my best friend that works for me, not against me. Laying around too much can eventually backfire so I do have to be careful.

Around 9pm this evening the head pressure took on a completely different level. I couldn't even lay my head on propped up pillows. The ice packs also weren't giving me any relief. I couldn't hear out of my right ear and the pressure was quickly shifting to both sides of my head. I had that gut feeling that something wasn't quite right and it wasn't going to get any better so I made a very, very critical decision to head back up to the hospital. It was the fastest drive of my life because I was in some serious pain! I also made a very quick and dumb decision driving up by myself. YES! THAT WAS DUMB! I could had not only killed others on the road but also myself. I just had a concussion but I feared the ride in an ambulance would be far worse so in ten minutes flat I arrived at the hospital and was taken back to trauma room #1. A medical staff of five quickly awaited me once I made it through the door. They take head traumas very seriously and so do my doctors who are concerned since I already have a seizure disorder. The emergency room staff was very fast and extremely knowledgeable. What they realized very quickly was the blunt force between hitting the wood table and the force of a 50 pound dogs skull caused the entire right side of my brain to bruise so the medication I was taking wasn't enough. I was still getting lots of new inflammation. The way I also hit a moving and standing object affected my ear drum so I am now getting inflammation in between my ears. This caused me to temporarily lose my hearing in my right ear but in time once my brain heals it will come back. Funny enough I lost my hearing in the same ear for months when I was recovering from Meningitis.

They gave me a shot filled with what they call, "The good stuff!" It was a three in one for the head pressure and crazy sensations I was feeling, severe inflammation and hopefully to get some much needed sleep. After the doctors thoroughly examined me they came back in to go over what the heck was making me feel rapidly worse this evening. They call it "Post Concussion Syndrome." I thought I heard it all but I guess you never really hear it all. Seems since I had two hits at once my brain couldn't handle that kind of impact so my brain is bruised and trying to start the recovery process. He explained it will take months and sometimes can even take up to a year before I make a complete recovery. I tend to think maybe a few months but once I learned since I already suffer neurological problems such as the seizures and vagus nerve issues it will most likely take a bit longer. GO FIGURE! Not the news I wanted to hear and I am so sick of being sick. I was extremely disappointed. The doctor said, "Instead of taking two steps forward you just took two steps back." With your past history of Meningitis and having a current seizure disorder it will take you longer than the average person to fully recover from the concussion." He did understand the reason I drove myself to the hospital was because of the overwhelming head pressure. At the same time he didn't agree with me making such a quick decision and instead I should had called for an ambulance or someone to drive me to the hospital.

Live and learn.

So after getting some medication and the doctor writing up a new prescription which hopefully will allow for some sleep and less crazy head sensations they went over Post Concussion Syndrome and what to expect as my brain recovers from the trauma. If I didn't like being stuck on my couchbed before I sure won't be liking it now! They do understand my Gastroparesis and did agree its important to still get up every so often and move around. They also understand the importance of doing my treatments. Honestly I was only able to do half yesterday because I just wasn't feeling well but half to them was better than nothing at all. My own doctors also agree but I do need to finish the rest of the treatment within this weekend. I just have to do the best I can for the time being.

At least the hospital doctors understood the irritability and said it was perfectly normal because its like having a huge bruise. Instead of having it on the outside its on the inside. They said, "Your brain isn't made to be hit with that type of force against your skull." I was warned I might experience other neurological changes and that its to be expected while my brain is in the healing process. I just need to try and not let it freak me out. Same with wanting to cry out of nowhere over nothing. Its also normal.

I left with me and my car being drove back to the house. I was beat! I just wanted to get back home with the fur kids and hope to goodness the medication will allow my brain for some sleep. Its nice to be educated on what I am going through as well the long term process of healing. Any errands that need to be done outside the house will have to be done now by others because the risk of me right now blacking out or falling are far too great. I sure don't need to play the medical lottery this time and get two concussions in a row.

Watch out couchbed! Here I come!..


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: January 20, 2012 12:49 AM EST
Post Comment | Permalink
January 17, 2012
DraCussion=Drano & A Concussion
Mood:  down
Now Playing: Day 641-The Final Road To Survival

What's a DraCussion?

Seems lately I am creating my own words...

Its when you have to endure Drano while having a concussion.

This would be a very, very bad day and if I woke up irritable just add ten times that when I learned I still have to do treatment. Of course things had to go through my specialists but was told this afternoon that they don't need any additional problems and take the concussion very seriously. I told them I honestly just want to rest in a nice quiet and dark room. Although I don't need a bowel obstruction going on either they felt it was safe for me to do half of the treatment today then finish the rest tomorrow. GEES! So after a horrible night of rest and waking up feeling worse than yesterday I had to motivate myself enough to get the hellish jug of liquid dynamite together. I figured the sooner I finish treatment the better off I will be!

Oreo has been laying around most of the day. I am sure he probably also has a headache.

 My friend found this little bit of information online regarding a concussion:

"A concussion may result when the head hits an object or a moving object strikes the head."

He then said, "Looks like you got hit with a double whammy! A sitting and moving object all at once."

FUNNY GUY! FUNNNNNNYYYY GUY!

OK. I did want to laugh but I am in too much pain so instead I just shot him a look. Hahahaha! I am used to keeping busy even during the ole Hell-In-A-Jug treatments so this time around was a bit trying. I also have to cancel and once again reschedule my Gastroenterologist appointment because I am not to be out driving. The hospital doctor said, "If you endure another concussion while healing from the first one it can cause brain swelling and even death." OK. Need not say more. I will stay home and find things to do occupying my time. For now the only thing I am occupying tonight is the bathroom from the darn Drano, my couchbed in between the bathroom trips and the ice packs placed over my face and head.

My friend has officially taken over computer duties and cleaning chores around the house. I am already going nuts and this is day #1. I want to watch TV but the light and sound hurts so I did my best to adjust the settings and brightness. Vomiting that came on late night didn't help and who knows if its from my GP or the concussion. My doctors will be in touch during the healing process. If I need anything my friend can just give them a call. Its a huge sense of relief knowing I have a great team of doctors and specialists. When bad things and unforeseen circumstances happen is when you realize those who truly care. 


Posted by GastroparesisAwarenessCampaignOrg. at 10:32 PM EST
Updated: January 17, 2012 11:12 PM EST
Post Comment | Permalink

Newer | Latest | Older