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The Road Before & After Surgery
March 8, 2012
Enough Drano To Send BACK To The Ocean!
Mood:  d'oh
Now Playing: Day 692-The Final Road To Survival

I TEBOW MY DRANO!

Hee,hee,hee,hee...Yep, it was too good not to go there! Sometimes when faced with a ocean full of Drano you might as well find some sort of humor in it!

Ask my friend who had the job of picking up the box of Drano goodies today at my local Walmart pharmacy. Boy! did he ever have a few great stories to share! Hahahahaha! He said the pharmacy assistant even tried to hand him the information packet with the eight jugs of liquid dynamite so he chuckled and replied back to her, "Thanks! but we already know the drill since this is more than over 200 jugs already." He said the ladies jaw hit the ground and the line of people behind him waiting to pick up their prescriptions were silent as a mouse. He said, "You could hear a pin drop!" Lastly add the cashier's look on her face since he had to pick up a few things and check out with the already paid box of Drano. The cashier asked to see a receipt and then questioned what was in the box. So he replied, "Oh you don't want to know what this is but I will give you a hint. Think of Drano but only for the body." I can only imagine her facial expression but instead the woman looked at him and said, "Oh heck noway! I could never do that on a weekly basis." Hmmmm....Well I guess she would never make it past even one weeks worth of treatment! Hahahahaha! Its a different experience dealing with Drano aka Hell-In-A-Jug treatments. Another experience when the world shares the monthly pick up process getting my prescription.

I am once again enduring the treatment hangover from hell! I am dragging and honestly could be just content staying on my couchbed all day but the animal gang would never have it. No such luck although Pumpkin kitty didn't have a problem just lounging on his window bed all day. Lucky isn't he?! Instead I did my best to move around hoping to gain some energy. I am still taking my daily handful of vitamins as well liquids but I honestly don't feel any different. I still have yet to get any energy but will continue taking them to make my doctors happy.

We all finally figured out my strange stomach rashes that have been coming and going over the past year. We also figured out the problem with my hypoglycemia. During my last surgery they did find some issues going on with my liver as well inflammation. Unfortunately since my intestines no longer work and lack movement/motility my liver became fused to them. My surgeons could not get to my liver in order to do further investigating. It seems whatever is going on continues to progress and my Idiopathic Gastroparesis is also doing a domino effect on my pancreas and other GI organs. Its no wonder I am having one heck of a time trying to keep my blood sugar levels up and once I do get a decent reading on my monitor I am a few hours later right back down again. I also have dull, achy upper right quad pain that really was quite easy to explain. I just needed to ask my surgeons or look at my last op reports. DUH! Your liver works with your pancreas and your pancreas works with your liver. When one acts up and starts losing function the other will soon follow. A hida scan would show my doctors how much function I have left with both organs but honestly at this point why bother? If they can't fix the problem or cure it then why add something else onto my full plate? Its tough enough dealing with the multitude of issues due to this darn Gastroparesis. Heck, I am just doing good keeping up with everything now. Amen. So I have decided to not put my body through anymore extreme tests. I will continue keeping a close eye on both my low blood sugar and low blood pressure problems with my paralyzed organs.

Thanks GP! NOT!!

Friday I have my last test of the week and hopefully for the month or rest of the year. It sounded good anyways! Next week I am back to the dentist to repair the last two teeth on the right side but still have to find out if there is more damage again on the left side. Maybe me and my dentist need to just move next door to each other? This way I could just walk over in between treatments and get my dental work done. Hahahaha! Pretty sad when I see my dentist more than any other of my 16 specialists.

Thanks Drano! NOT!!

Hey, at least I can still find humor in life with bad news. To me the best medicine in the world will always be laughter.

"As you walk down the fairway of life you must smell the roses, for you only get to play one round."


Posted by GastroparesisAwarenessCampaignOrg. at 11:28 PM EST
Updated: March 9, 2012 12:37 AM EST
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March 7, 2012
Let's Help Raise Gastroparesis Awareness!
Mood:  special
Now Playing: Day 691-The Final Road To Survival

sup·port·ive

Providing encouragement or emotional help.

The one thing that is critical for a successful Gastroparesis journey is support. Being supportive to a patient means being caring, compassionate, understanding, kind, forgiving, defiant, strong and motivated but mostly having the ability to think outside the box.

Today was once again a grim reminder for me on how Gastroparesis can progress one organ at a time leaving a path of destruction. There is no turning back. There are no answers. There is no specific medication. There are no cures. What is there? HOPE.

I got an email from an amazing woman named Arlene who has a daughter named Brianna who also suffers from Gastroparesis. Brianna is only three years old and was born with Idiopathic Gastroparesis. Brianna's condition is chronic and terminal. Arlene came up with an amazing idea designing a clothing line called, "Bibi Wear" as well a cute teddy bear buddy named "Bibi Bear." Arlene was picked to be in a contest sponsored by Walmart called, "Walmart Get On The Shelf." The contest is a way for people to get their ideas out of their home and onto the shelves of the large retailer. Arlene is hoping to get both the clothing line and Bibi Bear available to the public so other children can have easy access and comfortable clothing that allows for quick change of any feeding tube/line. Bibi Bear is a special bear that allows a child to take with him/her when parents are not allowed whether it be surgical procedures, testing, etc.

I feel strongly that Arlene's ideas and creative talent are very important for not just Gastroparesis patients but others who suffer from various chronic terminal conditions.

Please take a few minutes out of your day to help Arlene & Brianna get "Bibi Wear & Bibi Bear" on the shelf! Let's together make a difference and at the same time help raise Gastroparesis Awareness!

http://www.getontheshelf.com/product/4562/Bibi-Wear-&-Bibi-Bear


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EST
Updated: March 8, 2012 3:57 AM EST
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March 6, 2012
I Feel A Full Moon Comin On!
Mood:  d'oh
Now Playing: Day 690-The Final Road To Survival

Oh yes! Its a full moon week and so far one heck of a strange one too!

So much for my dentist appointment. I slept horrible and so did Littleblue. Between the nausea, vomiting and pain my body is screaming for treatment today! Once I turned over and looked at the wall clock it was 1:30pm so I figured at least I had another 30 minutes to sleep before getting up but NOPE I didn't wake up until 2:45pm. DANG IT! My dentist appointment was for 3pm so I called my dentists office to explain that I had a very rough night and morning so I needed to reschedule my appointment. Thankfully my dentist knows alllllllll about my unique medical condition and totally understands my bad days so they had no problem moving my appointment to next week. Of course I don't feel any pain since I have so much nerve damage so that's a good thing! At this point I just need to start feeling better soon and hopefully this afternoons treatment might help!

Today was a day battling my insurance company. My Gastroenterologist has been dealing with them now since December regarding coverage for my intestinal treatment medication. Now they only want to cover one jug every three months when I need eight in a month. I was in no mood to start the day with any stress so after an hour battling my insurance company explaining the situation I was able to finally get them to approve the medical necessity medication. Of course this was after an hour explaining my medical condition and my doctor prior getting on them over three times this past month. Let's just say my treatments are rare. VERY RARE! In fact so rare the insurance company and drug manufacturer have never heard of such a thing nor having to do treatment twice weekly. This medication is only to be taken once in a life time prior to a colonoscopy or before surgical procedures. Maybe they need to use me as their research guinea pig. Heck! at least they might learn something from me.

What a way to start the day!

Since my dentist appointment was a complete washout I decided to go ahead and get my blood work done and tests at the hospital finally completed. I am only three weeks behind. OOPS! At least my doctor will finally be happy but I can't help it seeing my full plate has just been way too full and its hard to keep up with things in between treatments. After 5pm all our local hospitals clear out pretty quickly so we had no problems finding a front parking spot nor had to wait too long to register. It was just myself and another person waiting to get tests run. A woman was waiting but looked more like she might had been taking a late afternoon nap! Hee,hee,hee,hee! 

No complaints here since its flu season and the least amount of people the better off for this gal! By the time we sat down my name was called back to the room. The hospital staff member was surprised to actually see someone with a low blood sugar problem-hypoglycemia since most people she said have high blood sugar problems and are diabetic. Seems the other woman who was there for blood work had high blood sugar problems and was getting tested to see if she needed insulin. For someone who just had to get her finger pricked one would think she just got her arm chopped off. OWWWWW! That is all both me and the technician heard and we both just smiled then the technician said, "If she thinks that finger prick hurt she sure wouldn't want the needle in your arm right now and all these vials of blood that need to be filled." Nothing phases me when it comes to pain but I guess I haven't heard anyone like that so petrified of needles and one little prick of the finger. It might be good she doesn't have Gastroparesis because BOY! would she been in for the ride of her life when it comes to pain. AMEN.

On the way back to the house we stopped by to get my prescription refill of liquid dynamite. The pharmacist looked at me and said, "Why are you smiling?" I replied, "Its because I am waiting for you to give me some bad news and that the insurance company decided to go back on covering it so this is my give me the bad news smile." Hahahaha! He chuckled and said, "Nope, we FINALLY got it to go through but guess what? I haven't met anyone like you so we never carry eight jugs with 32,000 units of surgical bowel/colon prep so I had to order from the drug manufacturer. It will though be ready to pick up tomorrow." I smiled and said, "Looks like my friend will have to pick it up seeing I am stuck with the Hell-In-A-Jug treatment this evening and into tomorrow so I am bathroom bound for the next few days." We both laughed, hahahaha! I feel sorry for my friend who has to walk out of Walmart tomorrow with eight gallons and a Santa Sack of Drano goodies! WOOHOO! I think its a great UTube video in the making don't you?

We didn't leave Walmart completely empty handed. Since I ran out of candy once again doing the low blood sugar battle I stocked up then bought Littleblue a new chewie hoping to keep her busy while I have to endure treatment this evening. She gets super excited with new chewies! Oreo honestly could care less and the only time he is interested in them is only to tease Littleblue and start trouble. Hahahaha!

Even with name brand Drano compared to the generic they all still vary when it comes to taste. Kinda reminds me of how each treatment also hits you. This darn jug tasted like straight up foul stale ocean salt water! UGGGG! I had my friend take a sip and they gagged. It was one of the top five worse jugs to consume but I made it through glass after glass while staying busy around the house. I would like to say I stayed stress-free today but darn me allowed it this time to happen. I need to start learning to put a lid on it especially during treatment days because stress during treatment can be deadly. I know. I should already know better but I am still a work in progress. Live and learn and maybe next time I will remember "NO STRESS" since treatment will most likely now go into another day. Half this evening and half tomorrow just to get things working.

WHAT A START OF A VERY LONG WEEK!...


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EST
Updated: March 7, 2012 3:21 AM EST
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March 5, 2012
SNOW=HAPPY! WOOHOO!!
Mood:  happy
Now Playing: Day 689-The Final Road To Survival

Around 3am Littleblue kept looking out the window then she would come over to me and start howling. Of course this woke up Oreo who was sound asleep and even I was close to drifting off to lala land! OK. So after a few minutes of having Littleblue stare me down I got her leash and opened the front door and guess what I saw?

SNOW! BEAUTIFUL S N O W....WONDERFUL SNOW! GLORIOUS S N O W! (Yes, I was singing this too! hee,hee,hee,hee!)

I can't believe its snowing! WOOHOO! Just goes to show you the weather channels are never right. This was a great packing snow too! Although with it being 3am I tend to think if I started to have any sort of snowball fight the neighbors might think I lost my mind. Hahahaha! Instead Littleblue got to enjoy the snow and even played in it for a bit. We both love snow! Oreo deals with it but he won't last too long outside before wanting to come back into the house so once I let him in me and Littleblue spent a few more minutes enjoying it!

Although this was suppose to be treatment day I still have been dealing with the nausea and intestinal pain so I wasn't feeling safe. Tomorrow I have my second round of dental work then I must come back home to start the ole Hell-In-A-Jug. I guess I better enjoy today before being back down for the count.

This was a typical BLAH MONDAY. I was dragging all day with lack of energy and just feeling exhausted. My friend also felt drained so we decided to hit the road and head to an outlet mall that is only a 40 minute drive away. It might be a good thing it was pretty close because after only 30 minutes the spinal pain started firing up so we had to make a few stops on the way. Sadly I only lasted an hour at the outlet mall. It was a perfect driving day though and its so relaxing looking at the open road and all the untouched fields that haven't been destroyed by human hands yet. AMEN! Regardless of the pain it was a relaxing drive on the way up and back. We didn't buy anything but I just enjoy getting out of my house-jail and feeling a bit normal. Its nice blending in with the rest of society and putting Gastroparesis in the back of my mind.

I have a very long week ahead of me so the rest of the evening was spent taking it easy and catching up on bills. I sure hope tomorrow will be my last dental visit and I can catch a break for once! Its a different life when you are sick. You must accept your condition and embrace the changes it brings. What I will never accept though is lack of respect from others. So far my stress has been kept at a minimum as I continue making positive changes to live a better and higher quality of life.


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 AM EST
Updated: March 6, 2012 2:12 AM EST
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March 4, 2012
Sugar & Spice And Everything Not GP Nice!
Mood:  down
Now Playing: Day 688-The Final Road To Survival

Boy! If only Littleblue could talk! If only she could drive! Its mornings like today that I realize sometimes Gastroparesis not only leaves you extremely vulnerable but darn helpless as heck too!

Around 3am I started getting ice cold, dizzy and feeling a bit brain fuzzy. I stumbled into the hallway to crank up the heat then turned on the small heater in the living room next to my couchbed. That sure didn't work so then I put on an extra layer of clothes and socks. At this point I figured it might just be my blood pressure playing games with me due to my vagus nerve damage. Once I checked my blood pressure it was running its typical low but nothing too low to have me worried. Remember I had two pieces of solid chocolate at the mall earlier in the day then I had my normal chocolate at the house that I must consume in order to keep my blood sugar up. Surely there is NO WAY that my blood sugar could be low and maybe its just the opposite, a bit too high?...My doctors always tell me its a must keeping sugar by my side! To any normal person who has healthy GI organs what I must consume would leave them with sugar readings in the 200's but not with my UFO body. I agree with them that I just can't break anything down nor absorb what my body needs. GEES! So I decided to get my monitor out and check my blood sugar levels and I was shocked! How the heck could my blood sugar be 65?!! Its not as bad as last week when it came up 58 but I wasn't feeling well and it was also after my Hell-In-A-Jug treatment. Hmmmm....So I made a phone call to my doctors on call line and was told I needed someone to run to Walgreen's or another 24 hour pharmacy to pick up some glucose tablets and gel. GEES! Of course Littleblue couldn't drive so I had no choice but to call someone to pick them up for me because I was far too dizzy to take the risk getting behind the wheel.

Around 3:30am the doorbell rang and my Mom was kind enough to pick up the glucose tablets and gel. I had already consumed some fruit juice as well half of a Gatorade and a bit of Slimfast. I was nauseated as heck too for downing whatever I could find but I don't need to pass out due to my blood sugar being too low. My Mom stayed for 20 minutes which was long enough to run my numbers again on the monitor. Anything over 100 is wonderful sound to my specialists ears and WALLA! 115. WHEW! Once my Mom left to head back to her house I called my specialist and was questioned why I didn't get the blood work and tests done he ordered over two weeks ago. OOPS! I paused for a moment and honestly said, "I meant to have them done but since I have to get the scan for the cyst in my chest next week I figured I would do both at the same time." It sounded good but it didn't work and I was firmly reminded things need to be done ASAP. Sooner not later.

One gets tired of dealing with tests and hospitals. Especially ME! Looks like this coming week will be a busy one. I already have my second dentist appointment to get my other two teeth repaired from the darn Drano causing enamel damage then I have the scan at the hospital and now I must fit in another visit to the hospital to get tests done for my pancreas, liver and kidneys. They are hoping to find a connection with my low blood sugar issues. Honestly I must agree with my Gastroenterologist that with Gastroparesis there is no turning back. The condition does progress over time and does effect all GI organs. That would include my liver, pancreas and kidneys. Maybe I just don't care to hear anymore bad news. Not that it would phase me. I have become a pro at bad news and its just something else to continue the good fight by keeping my boxing gloves laced tight! It is what it is sometimes but I must keep my team of specialists happy. They work extremely hard helping me to beat the odds and I should never forget that!

Drano day is scheduled for tomorrow but anymore it all depends on how I feel. I must listen to my body and heed any warnings before doing treatment. That means sometimes it might go into the next day but I have already grown used to it...

So this evening I took it easy and once we got home from running a few quick errands I kept busy doing some odds and ends around the house. Even feeling tired and beat I must always remember gravity and GP are best friends! Amen.

Thank you to my dear friend Arline for the beautiful ocean stones all the way from Florida. I couldn't agree with you more by saying, "One just never knows what luck the ocean can bring to others."


Posted by GastroparesisAwarenessCampaignOrg. at 11:52 PM EST
Updated: March 5, 2012 4:37 AM EST
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March 3, 2012
Staying Focused & Staying Grounded!
Mood:  cheeky
Now Playing: Day 687-The Final Road To Survival

 GP Life Motto: Try, Try, Try and Try Again!

Today is a day I am determined as ever to find something, anything at this point that will make my Gastroparesis and connected problems a bit easier. AMEN! So far it has been around four days since starting all the vitamins and I haven't felt much difference as far as energy. Heck, I didn't wake up till 3pm today and could had just slept in all day. I am beat! I dread this next Hell-In-A-Jug treatment and just hope to goodness it isn't near as wicked as the last one.

Since I am still dealing with nausea and intestinal pain I figured this might be a good day to head to the mall and get some walking/exercise. They say even light exercise helps the digestive process as well maintains good blood sugar levels. If that is the case I might as well walk to China! Hahahaha! Honestly after stopping at the Godiva store inside our ritzy upscale shopping mall and getting two pieces of dark chocolate candy I was still feeling a bit dizzy and off balance. I am sure my MS isn't helping matters nor low blood pressure problems due to my Gastroparesis but give this gal some credit because I walked both levels of the mall. WOOHOO!

My friend walked around with their jaw on the ground seeing this mall is full of people who know the word: EXCESS! With high end retailers that scream $$$$ and endless woman with more botox and silicone that could stop any pool leak it was clear to me these people were not in the land of reality. Once we passed the Apple store one would think they were giving phones and laptops away. WOW! What I was really thinking was maybe these people need to put the phone idea to the back of their over stuffed pocket books and instead take that money and help some of the families who lost everything in yesterdays vicious storms. Amazing isn't it when your sick and you can smell snotty, rude and obnoxious folks from miles away?...I wasn't impressed by the lack of common curiosity with the over rated mall and its over rated bad taste in clothing people (not to mention is Edward Scissor Hands their hair stylist?) who walked around with their noses up in the air.

Sorry but YES! I went there! Hee,hee,hee,hee

I guess you can say this normal, genuine, down to earth gal doesn't fit into their clique. Instead I left that mall thanking myself for being "ME!".

After taking a walk in another world we decided to go back to the house seeing I was still feeling off balance and this boat feeling needs to dock soon! With all the new things I am doing to see if it helps improve my health I am also back to every other day juicing. Scary enough near the good stuff is the jug of really, really bad stuff. YIKES! Its enough to scare the food out the refrigerator! Hahahaha! Two more days to go before another treatment begins. My how time flies by when you are faced with fun in a jug...

Later this evening I played with the fur kids a bit to get some of their energy out since the backyard is too muddy for them to play. Hopefully we will see a week of some dry weather for a change! With spring just around the corner I can only imagine how this season will effect my head issues on top of my GP. Ugggg!

For now I am keeping focused and staying grounded trying change after change after change. You never know, maybe I might get a huge surprise and something might just work! One can only hope!

"Life is a coin,
You can spend it anyway you wish,
But you can only spend it once."


Posted by GastroparesisAwarenessCampaignOrg. at 11:58 PM EST
Updated: March 4, 2012 5:02 AM EST
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March 2, 2012
The Calm Before The Storm...
Mood:  hug me
Now Playing: Day 686-The Final Road To Survival

I came close to another record breaking time before finally being able to sleep! My brain finally won the fight dealing with the burning pain, nausea and vomiting around 7am. I started my new meds but of course it could take 2-3 days before I see any relief. By then I will be right back to drinking the darn liquid dynamite. It just never ends. Its like a bad replay of the movie, "Groundhog Day."

Since I mostly did nothing but tossing and turning I also kept Littleblue and Oreo up. By the time I turned over to look at my cell phone it was going on 3pm. Talking about sleeping the day away! WHEW! I knew from watching last nights weather we are suppose to have some wicked storms today. At least at this point I better get up and take a shower then do anything that uses electric before the wicked weather arrives. Since my house falls on the same grid line as the huge mansions down the street with enough trees to fill a forest I am always prepared for the worst when bad weather is in our forecast. Me and my friend got together flashlights, candles and also made sure the back up sump pump was working. Last thing I need is another flood in the basement! As quickly as I got out of the shower and got dressed the lightening and thunder had already arrived. Thank goodness my friend took the fur kids outside once I got up because the wind and rain was horrible! On top of that we had tornados popping up all around us. This afternoon literally turned into a weather nightmare. Later this evening those who live in the area realized just how fortunate we truly were since they estimate so far around 17 tornados in just a few hours. How we escaped I have no idea but someone must had been looking out for those in the surrounding counties. Sadly some were not so lucky. They say during the worst crisis is when you find true heroes and those who risk their lives to help others.

Please keep those who were affected by the severe storms and tornados living in Ohio, Kentucky and Indiana in your thoughts and prayers tonight. If you have time to donate please do so to the local Ohio, Indiana and Kentucky Red Cross.

http://www.redcross.org/where 

Please also keep the beloved fur kids in your hearts and help all the rescue teams by donating to the animal rescue team of the "Humane Society of The United States" or send donations to your local animal shelters.

www.humanesociety.org

We were some of the lucky and fortunate ones who only sustained high wind damage. Picking up fallen tree branches is minor compared to those who are left picking up their lives.

Numbers 6:24-26
"The LORD bless you and keep you; the LORD make his face shine upon you and be gracious to you; the LORD turn his face toward you and give you peace."


Posted by GastroparesisAwarenessCampaignOrg. at 11:55 PM EST
Updated: March 3, 2012 3:08 AM EST
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March 1, 2012
Hellish DraNO Treatment Side Effects Continue...
Mood:  don't ask
Now Playing: Day 685-The Final Road To Survival

This hasn't been a very good day.

At least I did my best to set the cell phone alarm for 10am so I could pay my respects to my neighbor at the funeral visitation service. I know Jerry totally understood and respected my condition and what I go through on a daily basis. Since I have lived here for over eight years he has personally seen the ins and out with Gastroparesis as well the progression of my unique medical condition. The least I could do no matter how sick or horrible I was feeling was to pay my last respects back to him. I would had crawled there if need be but instead once I got up at 10am we tag teamed the wake up house duties, let out the dogs, fed the kitty gang and quickly got dressed and headed out the door.

Visitation was between 10-11am followed by the funeral service. I still look outside the kitchen window and wait to see Jerry and his beloved fur kid Lady dog head out for lunch on a car ride. Its strange when you realize how life can take such a drastic unforeseen turn. The church thankfully was only around ten minutes down the street so we got there with thirty minutes to spare. The weather was perfect today with a bit on the spring side. I am sure Jerry would had loved the clear blue skies since he was licensed in amateur radio. His towers worked best on days like today. It was a very nice visitation service and there was even a huge screen showing slides of Jerry's life. He sure did have a love for animals. Something we both have in common. He might not had physically traveled the world but all the postcards he collected over the years using his radio one would think otherwise. I never knew he enjoyed country dancing as photos we looked through showed a very happy Jerry embracing life. The good ole days! His daughters shared stories about how their Dad would talk about us; his neighbors and how much he appreciated the friendship and little things we did for him. Jerry had even collected holiday card photos over the years which were placed in the photo album. I had to chuckle and was a taken back a bit looking at a young blond haired woman who was ME! WOW! This was obviously the first year of my Gastroparesis diagnosis and when we first moved into the house. My friend had to do a double take and could only say, "WOW! That's YOU?!" Yes, for me it was also the good ole days but looking back at some photos I realized just how far I have come and for the better. Funny how life works isn't it? It was wonderful taking a glimpse back in time and I am so glad to have had such a compassionate and kind hearted neighbor. He will truly be missed but never forgotten.

Once we got back home the intestinal pain, nausea, vomiting and burning got worse. I wanted to go right back to sleep as planned but with the pain there was no laying down so instead I had to walk around the house for an hour before getting some relief. What doesn't go down will always come up or find a way out. This of course was wave 1 of 5 today. Not a good GP nor head day. As my specialists have realized and once again I personally found out both issues are connected. When my head fired up my intestines fired up then my stomach fired up. When my GI tract calmed down then my head started so after a full day that went into the evening of suffering I called my doctor to get some relief. AMEN! I am hoping to slowly rebound from the Hell-In-A-Jug side affects that were far from kind this time around. Sadly I am due once again for another treatment in three days but for now since my intestines are inflamed, burning, raw and quite angry its best they said to wait the next treatment out as long as my body allows. For now I am doing my best to keep liquids down and finding things that don't make the burning sensation any worse along with the nausea and vomiting.

Forget making good on going out once a week. This weekend will be a very low key one for this gal called, "HOMEBOUND." The way I have been feeling the last thing I want to do is much of anything but find a way to get comfortable on my couchbed. With the snow they are predicting starting tomorrow it will just be nice to finally see winter for a change and all the Angel kisses (snow).

First thing on my list tomorrow is calling my Gastroenterologist for the third time in less than two weeks since once again my pharmacist called to let me know my insurance company is refusing to cover my treatment aka Drano. They will now only cover one jug every three months! YES! YOU GOT TO BE JOKING ME! Its not that they can't cover it, they just won't nor give my head pharmacy manager any reasoning behind their decision so now my specialists will have to send an appeal letter for medical necessity medication to be covered. If this fails again I will have to pay for weekly treatments out of pocket.

WELCOME TO MY GP NIGHTMARE! Need I say more on this blog for today? Nope. I think not...


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: March 2, 2012 2:53 AM EST
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February 29, 2012
Drano Hangover From Hell!
Mood:  d'oh
Now Playing: Day 684-The Final Road To Survival

I just knew since this last treatment hit me way too fast I would still be paying for it a few days later. Here I am and on top of no sleep I have the worst pain as if someone lit a torch around my stomach. FLIPPIN OUCH!

A dear fellow GP friend said after their treatments using magnesium citrate it feels as if someone lit a match to their insides. AMEN! Lets remember this stuff isn't meant to be taken on a daily basis. This goes for the Hell-In-A-Jug I must endure in order not to become toxic and also for those who have to consume magnesium citrate by the bottles on a weekly basis. Yes! this is life and a crazy GP life it is!

Since I can't eat I figured why not try to get my mind off the pain, nausea and waves of vomiting by cooking for others. It was a great idea to get my mind off of everything and it always helps a bit to stay busy! I opted for my mixture of fruits and vegetables I juiced from my Jack Le Lemme machine, Slimfast, SmartWater, MetroElectro Water and a 8oz bottle of non fat chocolate Nesquik. Zero solid foods seeing drinking liquids already aggravates my angry insides quite enough! At least the overload of vitamins I now have to take on a daily basis might help me a bit. So far I can't tell much if any difference but its only been three days. I am back on my treadmill in the evenings hoping to get some relief from the stomach and intestinal pain. Let's just say I am drawling straws here and willing to try anything to keep me out of the local emergency room. With flu season just now starting I am also back to wearing my masks when out in the public. I will have to continue through spring and summer when allergy season they are predicting will be the worst yet. My head can wait!

I got some beautiful yellow roses today and it was exactly what I needed to brighten my day. The fur kids enjoy smelling them although one of the fur kitties decided to take a bite out of one of the roses this evening. It must not had tasted so pleasant because they left the half chewed piece on the table for me. Hahahaha!

After a not so nice head and Gastroparesis day I told my friend to get the Wii system together so I could get my mind off things. Once I got out of the shower and changed clothes I was told all my Wii games went POOF! I honestly thought it was an early April Fools Day joke since I moved them to a wall storage cabinet near the game system. I not only checked there but the other storage cabinet and sure enough all 10+ games since I lost track how many I had now had disappeared! I won't say where they went but word to the wise: When someone has an addiction problem and you keep giving them chance after chance to change just remember people don't change until they want to change and become a better person. What a really shallow thing to do taking games and something someone enjoys doing to help keep their mind off pain from being sick. Lesson learned from my end! Nice is as nice does and nice isn't being given out freely anymore. AMEN!

Late this evening before I got my couchbed together to relax and watch some TV a friend went up the street to buy three new Wii games to start my new collection. What a very kind thing to do and it goes to show you kindness is not all gone in others nor is my faith in people. Maybe I need to get the four wig heads to guard this new collection since four brains are better than one! Hahahaha!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: March 1, 2012 3:49 AM EST
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February 28, 2012
6 Years Later...The GastroparesisPatientsgroup Anniversary!
Mood:  celebratory
Now Playing: Day 683-The Final Road To Survival

One idea 6 years ago completely changed my life. All for the better and I am also a better person for it!

6 years ago I created the "Gastroparesispatientsgroup" sponsored by Yahoo. It was a place I created for Gastroparesis patients, their family, friends and loved ones all around the world to gather and support each other. A place everyone could go and ask questions, exchange ideas, vent and most important to connect and find lifetime friends. I am happy to say every goal has been attained and the online GP family has truly been a huge blessing in my own life. I call them my family and I am sure everyone in the group also agrees because there have been friendships established that continue to test the hands of time. We are a tight knit family and what one goes through we all go through together.

I want to say, "Thank YOU" to all my fellow GP family members for being my rock and strength during some of the most difficult times in my life. You have all taught me so much over the years as you continue to inspire me to become a better person.

These are some photos of the GastroparesisPatientsgroup online family. Happy times not sad times because even GP patients need a break from suffering and to be able to enjoy a moment in life to smile.

Here's to 6 years and many more to come my dear friends!

"In Memory Of Shannon, Brina, Scott and Impy."


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EST
Updated: February 29, 2012 4:09 AM EST
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