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The Road Before & After Surgery
November 22, 2011
Here Comes The Holidays!
Mood:  d'oh
Now Playing: Day 585-The Final Road To Survival

No matter how you slice it (if only us GP patients could eat more things that are sliced-amen!) here comes the holiday season! Its the crazy time of the year full of hustle and bustle. The time of the year when everyone goes broke then POOF! it is gone!

What happened to the days when Christmas was about visiting family, friends and loved ones? More so "FAMILY." What happened to the days when being around family was something you looked forward to? What happened to sitting at the table with family and catching up on each others lives? Seems those days have been replaced by cell phones, Ipods, computers and Wii systems.

AHHHH....THE GOOD OLE DAYS....WHERE HAVE THEY SADLY GONE?

It all got somehow lost. Now we push the holiday season with a huge serving of retail mumble jumble. Who really cares if you can get started on Black Friday at 12am instead of 6am? Did we forget about those employees who are now forced to work earlier due to a poor economy? Remember these faces who are now having to give up additional precious time with their families so society can find something else to fight about like HD TVs and video games on sale. Did we all somehow forget the true meaning behind the holidays? What about Thanksgiving? Did we all forget it is a day to pray and say thanks for the blessings we have in our lives? To say thank you to God for waking up and breathing in life another day? 

I have many things to be thankful for. Don't you?

It makes me sad to hear from so many who dread the holidays due to confrontation with family. Family who very seldom even see each other whether alone communicate during the year with even so much as a simple phone call to say, "Hi! How are you doing? Are you still alive?" Now you have to either be a member of Facebook or Myspace to know if your relatives even exist.

Such a sad society we have all become.

This Thanksgiving I am thankful for defying the odds that will always be against me. I can reflect back on a life full of triumph! I continue to prove miracles do exist and sometimes people can overcome great odds because maybe they are still needed on earth before they can continue their work in Heaven. I send my blessings to you and yours that maybe you too can find things in your life to be thankful for. Maybe you can take the time to put down those electronic devices that seem anymore to define the very heart and soul of us as human beings. Find time for family and never take life for granted. Never take family for granted either because when the day comes you want to be surrounded by those who supported you and cared. Not surrounded by people called family who have become strangers because they didn't take the time to genuinely care. Sure, you will always have those who would rather find things wrong or to complain about but not to fret seeing I personally have learned over the years those same individuals just haven't gone through enough tough battles to truly appreciate life. Sometimes you have to just let others be happy with their own behavior and move on.

 Keep lessons learned closely by your side and become a better person for the hardship.

This is the first year I have learned to put differences with others behind me. You can't change people but you can change how you react. Close the door and never look back. I have now made the holidays a time for "me" to enjoy whether it be by putting up a few trees, listening to my favorite holiday collection or placing loose change in a donation box. I now look forward to the holiday season. In this day and age I guess you can consider me a "rarity." Anyone who has overcome great odds can always find a reason to celebrate life even around those who are not listening. "TURN OFF THE FLIPPIN CELL PHONE FOR CRYING OUT LOUD!"

Hahahahaha! Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:58 PM EST
Updated: November 23, 2011 3:26 AM EST
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November 21, 2011
Drano UGGG Day!
Mood:  down
Now Playing: Day 584-The Final Road To Survival

You know what today is! It's Drano aka Hell-In-A-Jug Day!

Its also the start of a new week seeing this weekend was full of nothing but holiday decorating. The only thing left to do today was redo the miniature white lights around the fireplace in the living room and run another strand in the dining room. Of course one has to stay active during treatment and this time around was more important seeing last treatment didn't work. I had plenty of house chores I saved for today so I kept extra busy!

Since last treatment didn't work I am hoping to get things moving by drinking a bit more liquid dynamite than last time. Darn if I didn't realize I was out of Hawaiian punch and forgot to pick up some this weekend! I guess I will just have to use Gatorade-Strawberry flavor to chase the foul salt water mix. Me and my friend didn't wake up until 2:30pm. Actually my cell phone alarm woke me up letting me know today was Drano day. Good thing though seeing I would had slept all afternoon. I am still drained and not feeling well. My doctor called this afternoon to let me know the news that I had figured all along which is the Golytely/Trilyte is causing my kidneys to not work properly. What isn't making my organs act up anymore? If its not the ole Hell-In-A-Jug then its the extensive nerve damage from my Idiopathic Gastroparesis. Luckily I have learned over the years to become a pro of accepting bad news.

IT IS WHAT IT IS. NOTHING MORE AND NOTHING LESS.

My doctor wants to see me again Wednesday this week and see how the two rounds of medication are doing however she is aware I need to do my twice weekly treatment today. Darn if you do and darn if you don't. To me its just one evil against another. When I have days like today as well knowing I have to endure another treatment I make sure to fill my days with as much laughter as possible. Me and my friend enjoy playing the game, "Who Am I?" The game starts off trying to mimic someone we know by talking just like them including hand and body movements. I tell you what, its so much fun and we both never laugh so hard!! Its good to find laughter in life because life sure isn't a bed of roses. Mine is more like trees of toilet paper, hahahahaha!

A friend of mine sent me a great email with different emotions and captured photos. I found this one to be so true called, "Love." It shows a photo of a woman walking hand in hand with her loved one. Clearly he is disabled but she still accepts him. If only others in this world were just as accepting and saw through illnesses and disabilities. If only they reached out and loved one another no matter how unique or how many limitations they faced. Maybe this world would be a far better place!

If someone doesn't accept you as the person you are today then maybe they aren't worth having in your life anyway. Only true/genuine people in the world will look past your limitations and still love you for the person you are today. Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:57 PM EST
Updated: November 22, 2011 12:49 AM EST
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November 20, 2011
Eight Trees & Counting!
Mood:  incredulous
Now Playing: Day 583-The Final Road To Survival

I don't recall having eight trees last year although Drano does sometimes not allow me to think clearly. Hmmm?....

My friend had drill-Army this morning although I didn't hear him leave seeing I am not only beat but this darn kidney issue is also not helping matters. Add onto it the holiday weekend decorating that is almost complete! YIPPEE! I didn't wake up until 2pm so it was another day of catching up on sleep. 10 hours is a lot to most but if Littleblue didn't wake me up I bet I could had slept another four hours. I was able to get a bit of a head start on the last of the great tree set up. Maybe I should had finished up solo or called Santa's shop at the North Pole because my friend is already getting holiday burned out after putting up tree #4, hahahaha! Add more holiday music playing, the sweet smell of peppermint then top it off with one cranky Elf assistant. OOPS! I meant "friend." Its not like I decided to buy eight trees this year, gees! They have accumulated over the years and last year I gained two. Every room in the house minus the basement and kitchen has a tree.

Call it a SUPER FESTIVE HOLIDAY HOUSE!

My friend calls it, "NUTS!" or better yet, "This is extreme, GEES!" I also heard the complaints of, "Oh my gosh, not this song again!" "How many artists are going to sing this same song?" I replied by telling him, "Keep it up and I am calling down at the jail to see if any of the cells are available." Hahahaha! Yes. He got plenty of sleep last night, over eight hours after falling asleep around 11pm. He's just a very cranky and irritable Elf.

Another great debate we have going on is the fact that the Bungals, OOPS! I mean Bengals stink. This is my opinion seeing every time they do really well in their division people in my city go extreme and get wayyyy too cocky. What happens next is the Bengals fumble and lose. I have called it plenty of times before over the years. Ask my friend Kevin whom we also get into this same debate. So...I told my friend I am getting a Pittsburgh Steelers jersey or coat and wearing it every Sunday out in public. Hahahahaha! That will teach em! GO STEELERS! Not only that but when I was researching team sportswear online for the Steelers I found this hilarious Steelers fan face for your tree! YES! Now you can decorate your tree! I told my friend I am going to buy it and place it on the tree next to the driveway. He said, "I will cut the tree down." I told him if he does so I will just buy one and put a Steelers face on every tree in the yard, hahahaha!

Later this evening once we started on the last tree I told my friend it would only take around thirty minutes. I might had wanted to add another three hours onto it because the last tree he forgot to put put down the base pole. He said and I "'QUOTE", "The tree looks fine..." The almost five foot tree looked more like it lost a few feet. Maybe it didn't take in enough calcium over the year, hahahaha! I should had taken a photo because it was HILARIOUS!!!! So needless to say we had a bit of assistance then finished the final decorations as well the other three smaller trees. They are the fur kids trees. Fur kids also need their own tree too so Santa Paws can visit them on Christmas.

After a very long last day of tree decorating we both were exhausted! More so myself seeing I don't take in many calories and my insides are still very angry. I got my couchbed and side cart together. My friend got his recliner ready for bed and the fur gang? Well...They said, "Thank you" and decided to take a seat where else? Under their trees of course! Looks like Pumpkin is hoping for an early visit from Santa Paws this year!


Posted by GastroparesisAwarenessCampaignOrg. at 11:58 PM EST
Updated: November 21, 2011 11:11 PM EST
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November 19, 2011
Patience Is A Virtue.
Mood:  happy
Now Playing: Day 582-The Final Road To Survival

All good things come to those who wait and patience is a virtue. I am not just a firm believer of that quote but also a lucky percipient.

Maybe it takes a bit longer sometimes than others. Take for example the holiday decorating this weekend and final touches being added on the wheelchair ramp. I woke up at 11am this morning by the sounds of a happy hammer and saw. I didn't wait one second but instead took my pillows and blankets then made my way to the new chair in the back bedroom. I was still very tired so in no time flat I fell right back asleep. With all the weekend hustle and bustle around the house I guess Littleblue and the gang were so tired even hammering didn't wake them up. Oreo made his way back in the room to wake me up at 5pm. Let's just say I caught up on all the sleep I needed! With taking the new medication to fight infection it also makes me very tired. I won't be able to do my next Drano aka Hell-In-A-Jug treatment until Monday. My doctor wants to give my body at least a few days to possibly help the medication start working this way I am not instantly flushing it out with the liquid-toxic poison.

My friend worked his full time job from 11pm till 6:30am this morning then went straight to drill at the Army. By the time he got home and finally was able to sleep it was 3pm. Talking about also being exhausted! He didn't wake up until 8pm as I did my best to be quiet as possible once I got up to let the fur gang outside. Littleblue must be having a lazy day too because once I started my second round of holiday decorating she took her stuffed animal friend and went back to sleep.

Once my friend woke up he got a bite to eat then helped me get another tree out from storage. He did admit this was the first year he put up a Christmas tree and decorated it. I tend to think its just a 'Guy thing.' Tonight was his lucky night seeing we decided to get the GP tree and decorations out. This is a pre-lit tree so much easier to put together. The GP tree was an idea from fellow Gastroparesis patients back in 2009. It was a way for everyone to decorate a tree by sending their own unique ornaments raising hope for a Gastroparesis cure. I like to call it, "The GP Tree Of Hope." Either way my friend did an amazing job putting the tree up and helping to decorate!

I might not have the Elves this year to help me but thank goodness for another set of helping hands! It was a far less exhausting day setting up holiday decorations although there are still three trees left we decided to finish them up tomorrow. By 11pm once we got situated and I sat down on my couchbed I looked over to see my friend passed out on the recliner sleeping. I guess even he can't keep up with the fast pace of Santa's Elves, hahahahaha!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: November 21, 2011 8:53 PM EST
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November 18, 2011
Heed Great Advice! 'When You Want Something Done Do It Yourself!'
Mood:  celebratory
Now Playing: Day 581-The Final Road To Survival

Once again I found myself taking one of the best pieces of advice I have ever been given which is, "When you want something done do it yourself."

With Thanksgiving only a week away I usually put the holiday decorations up this weekend. This includes five Christmas trees. Last year I had help from the Elves but seems this year they must had went on strike because I started my first attempt solo. Of course I had my Supervisor Mr. Oreo helping on the job. More like after the first few hours, "Sleeping on the job," hahahaha! It must had been the decorations that set the tone for one tired Supervisor. The kittygang enjoyed finding tinsel that fell off a few decorations and played till they all passed out then fell asleep, hahahaha! Fur kids are just like children. They too get excited when the holiday decorations start coming out.

This year it might take me three or four days because unfortunately my friend has drill this weekend on his days off from his normal job. He doesn't just work full time at the local county Sheriff's department but is also active in the Army-14 years. Looks like this weekend I might have to call in some new helpers. I am still having severe nausea with waves of vomiting but like I mentioned before it is just a new thing I must learn to accept. Its not easy but its life and at least the peppermint oil I place on a piece of toilet paper or paper towel seems to help a bit at night. I place it right next to me on the cart so when you walk into the house my friend says, "It smells like one huge candy cane!" Hahahaha!

Once I finished up the first day of holiday decorating my friend thought it would be a great time to start working out. He has to work his normal job this evening-third shift so why not? Although every time I attempt to get back into the swing of working out I get sick so I don't expect anything less but if it helps him to get motivated then he can continue on his new work out routine. I chose to just walk on my treadmill as he braved the thirty minute 'AbTwister' machine. It was a bit funny watching him work out with the video. I couldn't help but to chuckle however he did make it through the work out with flying colors! I also made it through the treadmill although I must admit it did make my nausea a bit worse so I took my Zofran and called it an evening. My friend said he felt great after working out and hopes to keep up with the routine. I told him I will do my best to be his new work out partner but I couldn't make any promises with me being sick and having two lumbar fractures. He agreed.

Once my friend headed to work I braved another hour putting up more holiday decorations and decorated one small tree. It feels good to be productive at the same time battling my Idiopathic Gastroparesis. Its important even when you are terminally ill to have goals. Until I can't walk anymore I will always find a way to stay as active as my tired body allows. Let me rephrase that to more like, "When I can't walk any longer and my back finally gives I will still set goals but just a different way via wheelchair."

Guess you can say, 'THANK GOODNESS FOR THE POWER OF THE MIND!"


Posted by GastroparesisAwarenessCampaignOrg. at 12:09 AM EST
Updated: November 20, 2011 1:03 AM EST
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November 17, 2011
Let's Replay Wednesday Again...
Mood:  don't ask
Now Playing: Day 580-The Final Road To Survival

Hmmmm....Sure seems like its Wednesday all over again...Set cell phone alarm last night, wake up to Littleblue howling to go outside, feed the fur kids, tidy up a little bit then get ready to head to my doctor's appointment.

SAY WHAT?!

Did I just say, "Doctor's appointment?" Yes, I did seeing once again my internal organs are screaming something isn't quite right so is my gut. Unfortunately after my specialist attempted to treat me at home with medication that didn't work I am left with nothing but to suck it up and head to the doctors today.

I refuse to allow today to turn into another unproductive day. After realizing my car tags are up for renewal next month I decided to get that taken care of before my doctors appointment. I was told I can get handicap plates this way I don't have to worry about playing musical placards. I have one in my purse and one in my car but sometimes when my friend drives darn if I don't forget it. At least now I can just have it on my plates and put the other handicap placard in his car and leave it there! By the way did I tell you the new tags are free?! Yes, FREE! I couldn't believe it either, something finally that us who are handicap don't worry about having to pay seeing aren't the hefty medical bills enough?! So with thirty minutes to spare we headed down the street to my local BMV. It must had been a lucky day because there was no one else in line. WOW! Of course we ended up with an employee who was clueless on the new handicap plate forms for me to fill out but after ten minutes of waiting then getting my renewal tags we were on our day to my doctors appointment.

Speaking of also being lucky...I am fortunate enough to live within a short distance of all my 17 specialists like my doctor today who is just a few minutes away. It takes a team to handle my internal mess. I have a specialist per organ and honestly most will not cross their specialty seeing I have had the same specialists now for over eight years and they thoroughly know my unique medical situation. I am called their "Complex/Special Patient." Although most just call me plain "Lucky" or a "Walking Miracle." I would like to think I am both!

Once we walked into the office it was the same routine of signing in, going over my medical insurance, handing them my copay then taking a seat in the waiting area. Since it was already the start of a lucky day I was also the last patient being seen since they were nice enough to work me into their schedule. I only waited a few minutes then was called back into a room. My weight isn't the best it could be but my doctors totally understand when you can't digest food and you are always having to do Drano treatments it will be impossible to gain weight. I do the best I can but looks like Santa might need to bring me a few new pairs of jeans this holiday season because my size 2 are getting to be a bit too big.

My doctor greeted me with a 'Happy Belated Birthday' then proceeded to go over my symptoms. We also went over the medication I tried that for some reason just wasn't working. My doctor said, "You know your body better than anyone else so when something is wrong and you flag us there has yet to be a time where you weren't right." Today was no exception to the rule. The liquid dynamite in a jug I am enduring twice a week is starting to really mess once again with my kidneys. This would explain why over the past week I am constantly urinating and in the bathroom. Although the darn Drano didn't work this time around it still has to pass through my organs. The mixture is extremely harsh and toxic to my kidneys. What I thought was something else going on is just that, "Something ELSE going on."

SHOOT ME AGAIN! Does this look familiar or what?! Only difference is: New doctor, new shirt, new chair but different day, hahahaha!

So...to make a long story short I won myself two rounds of medication on top of my doctor having to send my urine off to a lab this way they can see first hand what kind of damage the darn Drano is doing to my kidneys. Honestly I am not really that surprised because the Hell-In-A-Jug is not meant to be consumed on a weekly basis. Its only meant to be consumed once in a lifetime either via colonscopy or as a surgical prep. Although as my own doctor stated, "Its important you still keep up with your treatments because it is keeping you from getting into trouble and causing bowel obstructions." Sadly looks like I have another serving on my already full plate but its just part of my crazy Idiopathic Gastroparesis life. I wouldn't be lying by saying after awhile you start to get used to the never ending problems. Lately I have been putting a lid on discussing my medical battle keeping it to under a select few except my friend who lives with me. I don't get into the full story or all the details seeing I feel its now best to keep things on the low. I am not getting any better but I also refuse to give up so I keep fighting each and every day.

This blog will most likely be my only outlet in the very near future explaining how I "really" am doing and why not? I don't feel the need to bring others down. I also would rather hear how other patients are doing in hopes maybe I can help them with their own GP journey. It makes me feel useful and I enjoy helping others. It also allows me to shift my focus to someone else which allows me time to escape my reality if only for a bit.

When you don't have local support and you had to become your own main support to a never ending battle after awhile you are OK with keeping mum. My friend said, "You are that way because you had to fight alone. You had to endure the blunt of things without having someone by your side. You were alone most of the time over the past eight years. You battled solo for such a long time that it made you super strong. You are a true fighter." It does make sense if you really think about it. I wasn't babied or pampered being sick instead I had to endure things on my own. So maybe its not fair but guess what? It's life. Now I don't have to be sick alone. I don't have to go to all the doctors appointments alone. I don't have to always be my own best friend but I am glad I learned how. Now I am blessed to take this next decade of my Gastroparesis journey with someone finally by my side.

So I chalk up today as just another battle to overcome. Including this evening as I once again have to bring out Mr. Puke pan, UGGGG! Things don't get better with Gastroparesis. Things progress over time. There are no answers. There are no cures. There are though people out in the world who do care and you don't have to go on your GP journey alone.

God is good and when you do good onto others eventually that help and support will find you. Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: November 18, 2011 2:12 AM EST
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November 16, 2011
Singing The Same Ole Song & Dance!
Mood:  d'oh
Now Playing: Day 579-The Final Road To Survival

Today was my new Neurologist appointment to get my back rechecked by the partner of my main Neurosurgeon. This appointment was also 'suppose' to be about going over the next step in order to allow me to live a more mobile life, 'back wise' anyway. This also became the second verse day to my tune called:

"THE SAME OLE SONG & DANCE"

Hahahaha! Seriously! No joke! I had to make sure and set my cell phone alarm seeing I didn't sleep very well due to the darn nausea that wouldn't calm down. I vowed today as well to head to my local 'Vitamin World' store and stock up on some good ole Peppermint Oil. I am not sure how many more Peppermint items I can have around the house nor consume but let's just say my friend has had their fair share and then some! With a sleepless night I ended up waking up before my cell phone alarm but my friend was dragging since they work third shift and just got home at 7:30am. Thank goodness they had nice chairs because he sure did catch up on more than a few zzzz's while I was back in the room at my Neurologist's office, hahahaha!

One quickly learns the dance steps of the "SAME OLE SONG & DANCE" after eight years and today I learned another new step to add to the mix! If your gut feels you are just wasting your time and being told something you already know then don't waste your time nor money having the same things repeated that you already know is going on with your body. Better yet maybe I should had been paid by my specialist and his staff today because they clearly have never seen someone like myself who is also still alive. After an hour of amazement and going over my Idiopathic Gastroparesis life story I not only felt like I educated my doctor but also a staff of ten. Sadly I could finish every sentence from start to finish on nerve damage, loss of discs in my lumbar-back, poor absorption with medication and connected problems that I have been enduring over the years. I was told once again, "You have some serious problems going on. Sadly I don't feel they can be fixed which also includes your back because the damage has already been done. We try to save people from exactly what has happened with your back and connected nerve damage. You have no discs anymore and now sitting on bone to bone which is causing you to have problems walking. It is also causing your spine to further shift. You need to use your cane on a daily basis. I am not sure if a full spine brace is a good idea with your severe intestinal problems because the compression of the brace can make things worse." The final line to the dance goes a little something like this, "I am sorry but sometimes there are patients like yourself that we just can't treat because we have no options."

SHOOT ME NOW!

So I read it like a book. This includes the entire visit but no worries seeing the old me would had left the room an hour into my appointment but the new me just took it with a grain of salt. I listened, answered questions, then answered more questions about my rare medical condition and ODD life. I guess if anything I don't chalk up today as a total waste of time nor loss because I was able to educate my new Neuro doctor and a staff of ten about Gastroparesis.All was not a loss.

On my way out I looked up to see my friend who was sleeping soundly in his chair while others smiled. Luckily after he heard my voice he quickly woke up, hahahaha! It was a sight to see indeed! POOR GUY.

I went today with an open mind expecting the worst but also hoping for the best. Instead I left today putting my lab coat back on playing my own best doctor minus the six digit salary, hahahaha! 

 If I can do it anyone can do it. Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: November 17, 2011 3:22 AM EST
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November 15, 2011
Crazy Day!
Mood:  don't ask
Now Playing: Day 578-The Final Road To Survival

It was a productive day yesterday and one darn CRAZY DAY today! WHEW! Just call it a little bit of everything all rolled up into one. At least with the rain and dreary weather there was less sun seeing it finally gave my head a break! It's been sunny enough the past week. The downside is with all this rain over the next few days it means the wheelchair ramp most likely won't be finished until this weekend. I guess if anything I can be glad for much needed rest and no loud hammers or saws waking me up. Same goes for my friend who had to work mandatory overtime this morning at the county jail and didn't get home from work until 12pm. He was BEAT! since he went to work yesterday at 10pm.

NO THANKS!

I got the wonderful privilege of dealing with another medical bill error today that started December last year after getting a CT scan at a facility that told me it was in network. A month later I get a bill saying I owe $1,750. NOT! Once I spoke to the head administrator on the error seeing my insurance company was never even contracted with the facility he clearly stated to me, "This is our error and go ahead, disregard the bill." Now almost a year later I get a statement from a collection agency saying I owe that same facility $345.00! WHAT?!!! I tried my best to remember my new resolutions for this new decade in my life and kept my cool but I have never had anything in collections so this was new to me. I tried contacting that same individual at the imaging facility where obviously they have some sort of miscommunication among themselves but of course they don't contact me. I was instead told by a billing representative that they did me a favor and wrote most of it off and was only charging me the remainder of the balance. MMMM....This was wrote off last year so there wasn't any balance to be remaining but I might as well been talking to a wall because the wall wasn't listening. My family agreed with me that this error on their end continuing for a year now just isn't worth the unnecessary stress so we paid the bill but not without me explaining the full situation with the collection agency. Not only did they listen but also told me, "Please write us a letter on everything you just told me as well a copy of the letter to the facility who wrote this bill off a year ago only in turn to charge it back to you again. We will investigate the matter with the imaging facility and get back to you. If it appears this is a situation that clearly as you stated was wrote off last year and there is a line of miscommunication within the facility we will credit you the money back on the bill." FINALLY SOMEONE LISTENED AND UNDERSTOOD! So lesson learned is this: Make sure you check and double check before getting any test done at any facility as well your insurance company that the facility is contracted with them. Never let anyone tell you it is or that they checked already because things like this can happen and no one terminally ill needs this type of unnecessary and additional stress. AMEN! Also if you are dealing with a mean, nasty and hateful spouse/ex who feels they don't need to help you with any bills and refuse to pay for any to put their name down as the responsible party with your medical professionals or any imaging facility, hospital, etc. ANOTHER LESSON LEARNED.

Once the crazy day started to slowly unwind Mr. Nausea started back up again in waves. Sadly the Drano never worked so I am trying to figure out which day might be best to start my second treatment this week. Terrible having to live and rearrange my life around jugs of liquid dynamite but it is what it is sometimes. I fixed dinner for my friend late this afternoon and made some stuffing with gravy. I got BRAVE and watered down a bit placing it aside for me to eat. DUMB MOVE! What I thought went down fairly well came right back up. So I can chalk up mushy stuffing onto my 'NO-NO' list. No wonder my specialists highly advise I stick with liquids especially since every time I now try to brave a few bites of solid food it comes right back up. Just not worth it.

There is a new show that me and my friend were wanting to watch and it finally aired late last night. The show is called, "MonsterInLaws" and boy was it FUNNY!! Kinda scary too seeing I could relate a bit with both new episodes that aired back to back. My friend sadly said they could relate too! It is a reality show if you want to call it but I say its more like "REAL LIFE." Just shows you once again what I always believed which is blood isn't always thicker than water. Maybe back in the day when family truly stuck together through the good times and the bad. Now in days families barely even communicate or know each other. Strangers now become more like family doing heart felt things reaching out to help one another. HMMMMM....Kinda like the concrete ground work that lead to the making of 'The Gastroparesis Awareness Campaign' over five years ago. A way for patients and their family, friends and loved ones to find support and not be alone nor feel alone. I guess you can say I would had rather been born back in the 1930's or 1940's. Maybe we all could take some of the lessons back then on how to treat family and apply them to our every day lives now. Amen.

Well off to visit the PorcelainGod and then hit up my Zofran...Here's to a better tomorrow!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: November 18, 2011 2:21 AM EST
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November 14, 2011
It Might Be Monday But I FEEL Productive! ;0)
Mood:  sharp
Now Playing: Day 577-The Final Road To Survival

Wow! Thanksgiving is only a few weeks away then you know what is next, CHRISTMAS! Where the heck does the time go? I know! One jug at a time or more like two jugs a week at a time, hahahaha! At least since the darn Drano didn't work during this treatment I saved some trees along the way! I wonder how many sheets it takes per jug of liquid courage? HAHAHAHA!

With it being Monday and a darn warm one outside too with this crazy weather it was a perfect time for me and my friend to finish up the last of the house cleaning. Maybe by continuing to move around I can move this blasted Drano out of my system although that is wishful thinking since I didn't get any further relief this morning or afternoon. You just never know how it will hit you and there isn't a doctor in the world who can figure out my scientific internal organs so things remain a mystery. Including the torturous weekly treatments.

My friend thought it was a good idea to head to the store which is right down the street by my house before the huge storm and cold front comes through this evening. At least with the store being so close to home I can make a quick run to the bathroom if need be but that as well was wishful thinking because the ole Hell-In-A-Jug continued the remainder of the afternoon to do absolutely nothing. Zip. Zilch. It was also a fast run through the store because when the nightmare poison lingers in my body it makes me sick, nauseated and BEYOND MOODY! WATCH OUT! Hahahaha! I didn't need to say anything to my friend because they have taken a few glasses for the team on a few occasions. Once we got home we rolled up our sleeves and brought back out the cleaning supplies. By 6pm we finished up the rest of the house which included two bedrooms, the upstairs hallway, upstairs bedroom and second bathroom.

IT FELT GREAT TO BE PRODUCTIVE!

Let's just say too much of a good thing is too much of a good thing and if my back could just separate and walk away this evening it would had done so because I was on fire with pain! I see my Neurosurgeon in a few days and know I am in for a good scolding. I won't deny being a bad patient but gees cut a gal some slack after years of going through nothing but pure hell. Amen! Once we finished up cleaning I figured it was a good time to take a shower and clean up while my friend cooked his dinner and finished the laundry. I got the PacMan World game on Wii as one of my birthday gifts so while I gave my body a much needed break and read the paper my friend got his Wii game-face on and enjoyed the remainder of the evening.

All good things do come to an end and it also holds true for my friend seeing his three day weekend came to a close. Back to the jail as he always says to babysit the bad guys, hahahaha! Just part of being a sheriff. I think he almost shed a tear as he headed out the door, tears of joy maybe to get away from me and all my moody-glory! HAHAHAHA!


Posted by GastroparesisAwarenessCampaignOrg. at 11:24 PM EST
Updated: November 15, 2011 12:01 AM EST
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November 13, 2011
Back To The Ole Drano...
Mood:  don't ask
Now Playing: Day 576-The Final Road To Survival

It's that dreaded time again. Time to get the glasses together for another round of ole Drano aka Hell-In-A-Jug. Nothing quite like starting the first week turning 40 with a jug of ocean tasting saltwater!

I had a wonderful birthday weekend and it was great getting out of the house! Seldom do I get to wear the nice clothes in my closet seeing I don't get out that much so this weekend was extra special! It was nice to dress up for a change! My friend even bought a few new sweaters and can also enjoy them this coming week as the winter weather slowly creeps up on us.  I love snow and was lucky enough to see the very first flakes of the season on my birthday.

Maybe its a sign of many good things to come! One can only hope!

Me and my friend decided since its Drano day which requires I stay active while drinking the toxic poison that we start cleaning the house. Not the typical vacuum and Windex but instead a really good cleaning with Pledge and the works! I thought it was a great idea and its nice to finally have someone assist with taking care of the house because its just way too much for this gal. Last time I attempted to clean the house it took me almost a week. YIKES! Once I got my Drano together and chaser of Gatorade seeing I ran out of Hawaiian punch we got our supplies out and started cleaning one room at a time. I can't bend down or stoop anymore so my friend was nice enough to do the hard cleaning and I dusted furniture that didn't require me to lift or move my back in ways to cause further problems. Once I finished up my last glass we got the living room, dining room, kitchen, hallway and bathroom cleaned.

TALKING ABOUT TEAMWORK!

Cleaning is a million times easier when you have help and it wasn't so scary like it used to be before I had my friend to assist. The Drano also went down a bit faster but not without a few times gagging and then getting things hung up. Sadly that sensation lasted for four hours and this treatment just didn't work, DANG IT! Typically a normal person would be in the bathroom within the first hour and making over 30 trips by now but not my UFO paralyzed intestines. Oh no! that would be too easy because instead by the time it was 11pm I only made two bathroom trips. I also didn't get any further relief the remainder of the evening so looks like another Hell-In-A-Jug treatment is in my very near future.

UGGGG!

I am sure glad I got out and enjoyed my birthday because I have a hunch this isn't going to be a very good upcoming week. Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: November 14, 2011 11:09 PM EST
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