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The Road Before & After Surgery
February 21, 2012
More Drano Issues? G E E S...
Mood:  irritated
Now Playing: Day 676-The Final Road To Survival

This is exactly what it feels like drinking the Hell-In-A-Jug on a weekly basis! Hahahaha! OK. So its not too funny during treatment but this photo just was too HONEST not to post! I think all my clean-out buddies can agree by saying, "Just put a straw in it!"  Maybe a different flavor too! Like malted chocolate instead of toxic ocean salt water flavor.

Today felt like Monday all over again. It started on the wrong foot but at least ended much, much better and I was able to get more than a few things accomplished off my huge week "To Do List." Just when I thought I had all the court papers completed POOF! there are two more sets to complete. Seems there is a reason why lawyers exist and it isn't always to represent you but just to do the arm length of papers that need to be filed out by our court system. After that snafu experience I headed to pick up my Drano prescription refill only to be told the insurance company once again refuses to cover it. Seems they don't understand over and over and over and over again why I am drinking colonoscopy/surgical bowel prep on a weekly basis since most people who lose intestinal motility have most of their intestines removed then get a colostomy bag. I tend to firmly believe they have never met a gal like me. Hahahaha! So once again I had to go through the same ole song and Drano dance: Call my Gastroenterologist, have him fax a medical necessity letter to the insurance company then contact the pharmacy.

It just never ends sometimes does it?...

At least once we got back home things turned to a more positive note. THANK GOODNESS! I got some wonderful news online from a private owned corporation and more great news coming from us both in June. I am also hoping to meet some fellow GP friends next month if the ole Gastroparesis permits but for now I have to take things one day at a time. The fur kids were on their best behavior and got two walks this evening. They were both very happy to get some time to play outside. The house chores are caught up and so is the wash. WOOHOO! I am on a roll and here's hoping that my dentist appointment tomorrow leaves me with teeth still left in my mouth. Hahahaha! YIKES!


Posted by GastroparesisAwarenessCampaignOrg. at 11:54 PM EST
Updated: February 22, 2012 12:32 AM EST
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February 20, 2012
DranoDaze...
Mood:  d'oh
Now Playing: Day 675-The Final Road To Survival

I have a Drano hangover from hell. I also didn't get to sleep until 5:15am after two hours of stabbing pain. Seems not only did the Drano aka Hell-In-A-Jug hit me way too late but it also got stuck in my lower intestine. The sharp stabbing pain started around 2:30am. Usually taking a walk helps to move things around and if my intestine is kinked up it will 'usually' help release it but not this time. We got the fur kids on their leashes and headed to the park across the street but once I started walking the pain got worse. Once we made it half way through the park I quickly had to turn right back around because the pain was getting to be off the charts. Its times like these when you must question how much more pain you can take and if its time to head to the emergency room. What I need to get is a stethoscope this way I can hear bowel sounds and find out exactly where they are coming from. Once I got back in the house I did my best to find a comfortable position then placed my hands firmly over the area where the pain was coming from and sure enough the darn Drano was stuck where my colon is fused to other parts of my intestines. I got to a 9 on a scale of 1-10 with the pain and told myself I could handle a 12 then it was time to head up to the hospital. Luckily around 5am after two hours of pain the liquid dynamite was finally able to move through the last part of my intestines and the pain started to ease up enough for me to finally lay down. I didn't get up until 2:30pm but am happy to say I did wake up pain-free. THANK GOODNESS! This next treatment I will be starting earlier!

We are suppose to have a rainy week. Not like we need anymore record rain. What we need is a month to dry out. The fur kids finally got time to play outside in the backyard to release some energy. They also got a few walks. With all the rain they are predicting it means things will soon be a muddy mess again so no more backyard fun time. I am so tired of the rain and so are the gang!

I got a call from my dentist and have the first of three appointments set for Wednesday. Not only do I see two new cavities but he said I had another one yet to be filled since my last visit. Thanks to my hellish treatments it is ruining my teeth and becoming beyond expensive! At this point my teeth are becoming the most the expensive part of my body and that IS SCARY! Maybe I should had false teeth put in a few year ago then I could just leave my dental problems at the dentist's office and pick them up later. Hahahaha! At least the kitty gang don't have to worry about dental problems but with the spring like temperatures they too are starting to shed earlier than expected. Once I get the brush out they like to run as I try to brush them. Most cats love being brushed but I think mine believe its nothing more than playtime. Hahahahaha!

This evening after switching from the Valentine's Day decorations to St. Patrick's Day Littleblue and Oreo finally called it quits and went to bed early. I guess all the nice fresh air got to them. I am hoping for the same. An EARLY evening! Amen! 

You will find as you look back upon your life that the moments when you have really lived are the moments when you have done things in the spirit of love.


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EST
Updated: February 21, 2012 1:36 AM EST
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February 19, 2012
DRANOFIED!
Mood:  d'oh
Now Playing: Day 674-The Final Road To Survival

I feel DRANOFIED! (Dedicated to my friend John who loves when I create my own words-hahaha!)

Here we go! Time to start a new week with the first round of liquid dynamite. I have a few appts already this coming week so I only have a few days open to do both treatments. UGGGG! My darn teeth are once again acting up due to all this treatment and looks like I have two new cavities needing to be filled. My next cleaning was suppose to be March 1st but right now I need to focus on the two fillings first! I also have a routine scan to check on the cyst in my chest that was found last year. I am already four months overdue and I am starting to get reminder letters from the hospital. My insurance company sent a letter yesterday letting me know it is covered under routine preventative care at 100%. Thank goodness seeing thats about the only thing they are wanting to cover lately. This is going to be a very busy week!

While consuming the nasty salt water with a kick I noticed it might be time to replace the ole couchbed and loveseat. The set is only four years old but I don't want to wait until its no longer in good shape to sell it. With it being tax refund season if I am going to sell it now is the time! I have the new extra large recliner in the backroom that has only been used around five times so I was thinking of just buying a sofa to replace the one I have now and putting both recliners in the living room where the loveseat is placed. This would allow for more open space and guests could use the recliners when visiting. The new sofa will be a bit larger than the old one which also allows for more room to sit. I cleaned them both up this evening and took a few pictures and placed the online ads. Hopefully it won't be a problem selling them so I can buy the new sofa before spring.

Lot's of new and exciting changes coming soon and I can't wait! Its about time for some positive news isn't it?! CHEERS!


Posted by GastroparesisAwarenessCampaignOrg. at 11:50 PM EST
Updated: February 20, 2012 2:25 AM EST
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February 18, 2012
Yep, It's Saturday...
Mood:  a-ok
Now Playing: Day 673-The Final Road To Survival

It was a horrible nights sleep as the waves of nausea and vomiting paid me another unwelcome visit. Just as soon as I was getting comfortable and ready to go to sleep which was around 4am it hit me in full force. Time to get Mr. Yellow Puke Pan back out again...GEES! That's the problem when you are hit with severe vagus nerve damage because it stems from the back of your head all the way down your GI tract. Nausea and vomiting is very common once the damage progresses. I have noticed a connection with the tremors because they tend to start right before the nausea hits then the last of it ends with vomiting then I finally get some relief. Since my last doctors appointments I was strongly advised to no longer take any anti nausea medication because it was just prolonging things. My body needs to work through the symptoms in order to move past them. Nothing quite like sucking things up but I figure if I can do it for years with the off the chart pain I can do the same with the nausea and vomiting.

I am due for another treatment tomorrow. I am starting to once again slowly get back into a routine with the liquid dynamite. With numerous fellow GP friends having horrible problems with bowel obstructions and being hospitalized as well one having two surgeries in less than a week I really can't complain too much having to endure the Drano. Why you may ask? Because it helps me from getting into the same trouble-bowel obstructions that can be deadly. What my fellow friends are enduring this week is nothing more than a eery reminder why I must stay on a normal routine with my treatments. I must still stay focused and far, far away from any stress. So far...So good as I continue making changes in my life to be stress-free.

Today was a day to catch up on errands and some house chores. I got mostly everything done with just a few things left to do tomorrow. With treatment and making sure I keep moving allowing gravity to help it will be a good thing I left some things for tomorrow. This evening I made some homemade Mexican for friends as I braved my first tiny cup of low fat ice cream yogurt. Most people could eat this in a few bites but my stomach just couldn't handle it. I made it through half the small cup then had to put the rest back in the freezer. I still haven't been able to drink half of a 32oz Gatorade on a daily basis yet but one step at a time. At least the homemade Mexican was a huge hit and there wasn't one clean plate left. Hahahahaha! God might limit me on what I can eat but he didn't limit me in the ability to still be a darn good cook! Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: February 19, 2012 4:08 AM EST
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February 17, 2012
Celebrating A Belated Valentine's Day!
Mood:  happy
Now Playing: Day 672-The Final Road To Survival

Finally its the weekend! I am beyond ready to get out of this house-jail and celebrate a late Valentine's day. Better late than never and so far it looks like a rain-free upcoming weekend too!

The fur kids have been extremely antsy wanting to run and play outside in the backyard. Littleblue has been non-stop shedding and it would be great to get some of this fur released outside instead of inside on the furniture.

Looks like there will be all sorts of new changes coming very soon! This also includes new neighbors. The house next door is no longer vacant and the new neighbors will be moving in this weekend. I am hoping to maybe have some new neighborhood friends. That would be great and maybe even a new playmate for my friend's son and even a few fur kids for the gang. Its perfect moving weather although I sure don't miss the time it takes to move nor the stress. Thanks but no thanks! Next time this gal moves it will be out of state to Nevada or to the cold weather and mountains in Colorado.

I made good on the promise to myself heading out at least once a week to have some fun and enjoy life. Tonight was the night although it was a very slow start due to the waves of nausea and vomiting. I figured it might be a short night when I was already yawning and getting tired before we even headed out the door. Hahahaha! There are so many new places I want to try up in the Dayton, Ohio area as well Northern Kentucky. At least I was able to visit one of them this evening although it was short lived. I just couldn't get my body to follow my brain and have some fun. My energy ran out after just two hours but "A" for effort and at least I gave it a good attempt! Luckily I still have a few great friends in the city, more than just acquaintances that totally understand my limitations that sometimes happen with my medical condition so we all decided to call it an early night.

When I arrived home the fur kids greeted me at the front door with wagging tails. I had a friend take a few photos of us celebrating a late Valentine's day near all the wonderful cards and gifts I got from everyone. This might be a low key weekend but that's ok because there is always next week to play catch up with living life and having fun! Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: February 19, 2012 3:17 AM EST
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February 16, 2012
A Lazy Fur Kid Day...
Mood:  chillin'
Now Playing: Day 671-The Final Road To Survival

One would think today was a lazy fur kid day...

Not that waking up until 3pm wasn't late enough but after getting two walks and a defurminator brush out the entire gang was done for the day! Hahahaha! I tend to think this crazy weather jumping back and forth from winter to spring is to blame. Everyone lately seems to be coming down with some sort of virus or horrible allergy problems. My doctors have warned me this is just a taste of things to come. I have a hunch this might be the worst allergy season we have ever seen and if so just send the plane and here I come the mountains of Colorado!

I can only handle so many days in a row stuck in the house so today I ran some errands even taking the fur kids along for the ride. Oreo needs his toenails clipped and since the rain has let up this was a perfect opportunity to visit his groomer. Littleblue is continuing to shed her winter coat a few months early and what a mess! I must now vacuum the house once a day in order to stay on top of the hair. Luckily I have a defurminator rack so every day she gets brushed in the basement. Its a two man job but we're hoping most of her shedding will be done by early next week. I always keep covers on the couch but with her shedding they must be changed also once a day. Its a job! Oreo has short hair and when he does shed it isn't much. Thank goodness!

Jingles puppy gets to visit with the fur gang once a week. He is getting to be huge and now weighs 30 pounds. Its good for Littleblue because it helps to get her energy out and allows for some play time however since Oreo still has seizure problems he chooses to remain out of the playing and instead in the hiding far away on the couch. Oreo will be 14 years old this year and let's just say he has earned his "leave me alone freedom." Hee,hee,hee,hee...The groomer did mention when she was trimming his toenails that he seems a lot more calmer thanks to his new medication. He doesn't have seizures as often so its a good sign! Since I had Drano treatment for Valentine's day the only ones who got to celebrate were the fur kids.

I made a promise to once a week treat myself to some fun and get out to enjoy life. I am keeping that promise and hoping to get out this weekend finding new things to do. Life is far too short and when I have a good day I plan on using it to the fullest. I completed my treatments this week and the last one was finally successful. The friends I have here in the city are fully educated on my unique medical condition and I now take a large purse with medical necessities just 'in case' something happens. My mind is much clearer and I am no longer scared because my doctors have been doing a wonderful job educating myself on remaining calm and keeping myself focused. I hope to continue taking small steps in order to plan a short weekend get away this coming spring. For now I am taking it one day at a time and one week at a time finding a new adventure to aim my sites on!

Lookout weekend because here I come!


Posted by GastroparesisAwarenessCampaignOrg. at 11:40 PM EST
Updated: February 17, 2012 2:47 AM EST
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February 15, 2012
In Memory Of Kellina Angel :0)
Mood:  special
Now Playing: Day 670-The Final Road To Survival

Life.

This afternoon I received very sad news regarding the passing of a life that was cut far too short. It was news regarding the littlest Angel that now is with other Angels in Heaven. A life full of suffering and a life full of courage. A life full of determination and strength doing what so many Gastroparesis patients as well others who suffer from chronic and terminal conditions do on a daily basis which is to fight to stay alive. Fight to live in hopes of a cure.

I have been blessed by those who have allowed me to be a part of Kellina's life. Kellina is a hero and shows us all in life we must remain strong. We must continue the good fight to live! Today February 15, 2012 at 5:35pm Heaven welcomed Kellina the littlest Angel. Kellina was only 3 years old.

The Gastroparesis Awareness Campaign Team and the Gastroparesis Patients online support groups send their prayers and blessings to our dear friend Jeannie & Kellina's entire family who never left her side. May you now fly with the Angels Kellina.

Image of the Angels
You were made in the image of the angels,
and all that was good up above.
A precious little star in the dark night,
Made with God's care, and with his love.


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EST
Updated: February 16, 2012 3:38 AM EST
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February 14, 2012
A Jug Of Dynamite On Valentine's Day!
Mood:  d'oh
Now Playing: Day 669-The Final Road To Survival

HAPPY VDRANO DAY! Hahahaha! For those of us GP'ers who are not so fortunate to have intestines that don't work and are past surgical options you all know exactly what I am referring to! YES! It's not just Valentine's Day but Hell-In-A-Jug Drano day too!

This should be a day full of chocolate candy dreams but the only dream this gal will be having is hoping this time around treatment will work. AMEN! My Gastroenterologist switched my prescription to something a bit stronger. Not quite sure how much stronger liquid dynamite can get but this one surely did work a lot faster than the last six jugs. WOOHOO! (Thanks John for now flagging me on my WHOAHOA typing error after how many blog topics? Hahahaha! Yes. I like to make up my own words!)

Early this morning I woke up to a huge Teddy Bear moving next to me on the recliner. I thought maybe I was losing it but nope, Pumpkin Kitty was doing his best to lay on Mr. Teddy Bear but instead only was able to put his paw on him. Hahahaha! It was a great photo opportunity too cute to pass up! Same with Oreo who is really enjoying the new living room furniture which allows for him to spread out on his big floor bed. Once I covered him up he was out like a light. Fur kids are so much like human kids aren't they?..

Regardless of a long Drano day that included constant moving around allowing gravity to work for me and not against me it also gave me a time to reflect on the blessings I have been given in my life. I am blessed for the amazing love and support from GP family, friends and so many strangers who I now call my friends but also family. I am blessed for those who look past my disability and still open their hearts and share their lives with me. I am blessed to have loyal friends here in the city who proved to me time and time again that blood isn't always thicker than water and have given me wisdom that will last a lifetime. I am blessed for an amazing team of 16 specialists who treat me more than just being their patient but as a friend. They have allowed me to live longer than ever expected by giving me the tools to continue to fight the good fight. I will always be blessed to know for all the times I felt alone I was never truly alone and have the support of hundreds upon thousands of people who truly care. Even those in the city who look out for my emotional and physical well being I just want to say, "Thank you."

To everyone who loves me and allows me to love them back, "Thank you and may you have a very blessed Valentine's Day!" I am beyond appreciative for all the beautiful cards and gifts. You are all the best! May God always bless you and may Hershey find you in heaven today. The chocolate kind! Hee,hee,hee,hee...


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: February 15, 2012 3:03 AM EST
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February 13, 2012
Keeping My Head On Straight.
Mood:  chillin'
Now Playing: Day 668-The Final Road To Survival

Thank you to those who informed me that I had two of the same similar posts. Blame it on the internet acting up last night but also blame it on the Drano. All good now and no, you weren't losing it or seeing what appeared to be the same post. Hahahaha! I went to hit publish and it kicked me back out so I did my best to rewrite it only to realize the blog was on delay. WHEW! Can you say that real fast ten times? Hahahaha!

I wasn't able to finish my Hell-In-A-Jug treatment today but instead earned myself a doctors appointment and another one via telephone. I was highly advised I need to watch my tolerance for stress and do better with stress management. I know my doctors work extremely hard keeping me from getting into trouble and I don't want to make their job any harder than it needs to be. They are also still working to put my head flair up back to sleep. Just because I might have a few good days doesn't mean I am completely out of the woods. I partly blame myself for not walking away from any stress that will only progress my condition. Its tough and each day is a learning process. Yes, I am still learning but no worries I am still focused and taking things one day at a time. What most don't realize is my unique medical condition involves extensive nerve damage. I was told a week ago my condition has progressed and what stress may do to a normal person it does far worse damage to someone like myself. It can accelerate things and place my doctors once again in a quick scramble to calm things back down. I need to always remember its a team effort and I must learn to work with them and not against them. This includes treatment that must continue again tomorrow. That is if I don't have to do another half treatment from not being able to finish the first one today.

Tomorrow is Valentine's Day and although I already had prior plans I must now change them. Unfortunately Valentine's Day celebration will have to wait until later this week but that's ok and I understand my health comes first. Patience. P A T I E N C E. Like I said, "I am still learning."

Serenity Prayer

God grant me the serenity to accept the things I cannot change;
courage to change the things I can; and wisdom to know the difference.
Living one day at a time;
Enjoying one moment at a time;
Accepting hardships as the pathway to peace;

 Serenity Prayer: What does it mean?
This beautiful prayer was written by a man named Reinhold Niebuhr in 1943. The words have special meaning to those who are often “looking for peace” at a time of turmoil, despair, or uncertainty in their lives. This prayer has become closely associated with 12 Step programs, offering strength and calm in pursuit of a more stable life.
"Perseverance and successes aren’t born out of good times. They are born out of trials."


Posted by GastroparesisAwarenessCampaignOrg. at 11:14 PM EST
Updated: February 14, 2012 3:05 AM EST
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February 12, 2012
Drano & Key Lime Pie!
Mood:  d'oh
Now Playing: Day 667-The Final Road To Survival

Sadly the snow is almost gone. At least Littleblue and Oreo sure did enjoy running around outside and playing. I can only hope Mother Nature pays us another winter snow visit this upcoming Valentine's Day week. To me that would be the ultimate gift! I love snow and winter but dread the upcoming spring that makes my medical nightmare that much worse. The fur kitties did nothing but find all the cold winter weather as an excuse to lounge around a bit more than usual.

Today is Drano day. UGGGG! I didn't get up until around 3pm today after using my energy over the weekend getting out to enjoy life. It was so worth it but my body was sure tired and needed the extra rest. My blood pressure today has been running low so it was an easy decision to only do half of my wicked treatment today then finish the rest tomorrow. I made sure to stay busy finding things to do around the house so I decided to make an early Valentine's Day gift. Its nice to do something special for someone else and food always hits the spot! Unless of course you have Gastroparesis. Amen! I decided to make a huge Key Lime pie. Nothing quite like Drano and Key Lime although I did have a few lime packets attached to my Hell-In-A-Jug. Even I would never ruin a good pie but darn could you imagine the taste and tart kick?!! WHOAHOA!

At least this jug of liquid dynamite didn't taste like warm plastic so it must be the manufacturer with the other ones. This time I got the large jug instead of the wide jug. Amazing what you discover after hundreds of jugs of Drano isn't it? Hahahahaha! I would love to know how many jugs I have consumed so far over the years but even sometimes life doesn't want you to know everything. Right? Right!

I have been noticing more tremors. I do fine if I just keep moving once I wake up but then at the end of the day once I lay down on my couchbed the motion sickness starts up then the tremors. Now I make sure to keep Mr. Puke Pan nearby! Regardless I am still thankful for being in the 'know' of my GP complications so I am fully aware of what I am fighting as I keep my boxing gloves laced tight! Amen.

Here's to Drano Monday! NOT...


Posted by GastroparesisAwarenessCampaignOrg. at 11:23 PM EST
Updated: February 13, 2012 2:55 AM EST
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