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The Road Before & After Surgery
March 22, 2012
OUCH!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Mood:  irritated
Now Playing: Day 706-The Final Road To Survival

Maybe instead of all these vitamins that might had been a great idea that obviously aren't working I should instead just take some of this left over Miracle Gro and drink it! Hahahaha! Heck, it might get my hair and nails to start growing again! Yes, I am still taking everything at least until they are gone but at this point since I see nor feel any change I highly doubt I will try them again. I used to do liquid vitamins a few years ago and back then I even gave up because it didn't help matters. At least I give myself some credit for trying again.

Today is time to give up and give in. I am going on three days with limited rest trying to deal with this spinal pain. I have finally hit my limit! I am beat and the pain feels like a knife stuck in my lower back. It is great I have a high tolerance for pain but something isn't quite right. I can't get comfortable. I can't sit down. I can't stand up without hunching or leaning over. I can't even go to the bathroom without the pain sheering down my left leg. I called my Neurologist but they can't work me in until early next week but they feel since things are getting worse and not better its time to get checked out. I have used enough IcyHot, Activon, heat wraps, ice packs, Aspercreme and Tylenol that still here I am with the same gnarling pain.

It might had been a good thing my friend was off work today since his off days rotate. I couldn't do much whether alone put on my shoes. I can't bend more than a few inches without my back locking up. At least I live in a city with way too many Urgent Care facilities and hospitals but even a short drive turned out to be a nightmare! The bumps hurt like a son of a gun and I was getting furious! I am also extremely tired but something isn't quite right and my gut is never wrong. So after an hour wait, lengthy medical review, tests and two xrays later the feared news soon became reality. If you remember last June I found out I had lost three discs in my back and had a slight fracture. I also was told I have spinal degenerative disease, spinal spinosis and osteoarthritis. I did see my Neurologist and another specialist only to be told surgery options were out of the question because the damage to my lumbar part of my spine were far too severe. The damage had already been done. I was told once again things would progress-funny same diagnosis with my Idiopathic Gastroparesis-but who would had guessed things would take such a drastic turn in less than a year? Not I nor my friend so we were both a bit taken back with the news.

It seems my poor spine since losing the gel discs between the vertebra bones has gotten worse. I now have pretty much lost all my lumbar discs and the once small fracture has also gotten worse. I ended up as well with a spinal sprain and broken back-nice term to say sorry but BOY YOU ARE SCREWED! The doctor couldn't even look at us with the news but only said, "I don't know what to do for the pain. I have no suggests for sleeping position because you have such extensive damage to your spine and back. I understand they can not risk surgery due to your pre existing conditions but the pain isn't going anywhere anytime soon." He was surprised I was still walking after looking at the tests and xrays. I think that made all three of us. Its still strange to image that is my spine! I said the same thing after my GI nightmare surgery four years ago and here I am saying those same words again. "Is that my body?"

A normal spine would be nice then I wouldn't be faced with knowing I will be wheelchair bound by the end of the year or sooner. It would be nice to have a normal GI tract and organs so at least I could eat to my hearts content and take some of this bad news out on a half gallon of ice cream. Instead I took the news like a pro and nodded my head understanding that once again things aren't in my favor. For now all they could do is find a way to get the blood flowing to my damaged spine with three different medications. The problem now is the medications can cause reactions with the Drano aka Hell-In-A-Jug treatments but right now I can't even sit on the toilet to urinate without wanting to climb the walls so how could I endure treatment to start with?

WHAT A MESS!

Once we got home with the bad news and another round of reports to give to my specialists I told my friend how much I will miss biking. Something I loved to do but life is full of changes. Especially when you are sick. I am in fear now of waking up not being able to feel my legs. I already have no sensation on the lower left side of my spine. I guess if things are going to end up with me being wheelchair bound at least I had a good past 10 months. Always savor the day! Live life to the fullest because you never know what tomorrow may bring.

This evening me and my friend shared quite a few laughs. Anything at this point to keep my mind off the pain and more bad news. Tomorrow is a new day and I am just hoping it starts off with me standing up on my feet. Amen.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 AM EDT
Updated: March 23, 2012 3:06 AM EDT
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March 21, 2012
Another Full Moon?
Mood:  surprised
Now Playing: Day 705-The Final Road To Survival

Wow! It must be another full moon. YIKES! What the heck has gotten into everyone lately? Maybe some of my Drano? Maybe so...

At least someone is drinking Drano. Not I. I am too busy putting out more stressful fires today. One good part of playing a Firewoman is by putting out fires it is keeping my mind off the spinal pain. I didn't sleep but four hours last night and kept waking up every other hour. This BITES! The pain is annoying and honestly one more day is about all I can handle then my white flag surrendering goes up!

The temperatures are still in the mid 80's but hopefully things will change by this weekend. At least they are saying so but with weather you can never predict the unpredictable. The kitty gang have been enjoying the afternoon sun upstairs in their huge cat tree. Since the large bedroom window is facing the backyard and woods they all sit there and watch the birds and squirrels all day. Boy, they still have an easy life don't they?.

My blood sugar hasn't been doing too well the past few days and today I woke up with it not getting any better. Between trying to get my blood sugar up all day then stress walking into my life early this evening it was in my best interest to not do treatment. Unfortunately it will have to wait. Its not the first time, in fact this seems to be getting into a routine that quickly has to stop. Amen. My friend is even starting to grow tired of the unnecessary stress and drama. What people don't understand is the responsibility placed on those who take on the caregiver roll. Not only do they have to protect the person physically but also mentally. My friend might had not been there once but he vows to never have it happen again. My condition at this present time requires someone staying with me. There is no way I could do it alone. My two other friends I keep in close contact with here in the city. They are very aware of my Gastroparesis and are ready when needed to step in when things get to the point that I need extra help.

As for my Hell-In-A-Jug treatment? It must wait for tomorrow. I do have an idea for those who question what one endures drinking this toxic stuff on a daily basis! Expect an Easter Drano basket this year on your front door step wrapped up in a pretty pink bow! Hee,hee,hee,hee...


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: March 23, 2012 2:14 AM EDT
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March 20, 2012
Use Your Brain-Not Your Heart.
Mood:  d'oh
Now Playing: Day 704-The Final Road To Survival

Where else but Ohio can you have snow then the next week summer weather and 85 degrees?

The pollen count has hit an all time high by setting records everywhere today. Just step out to your local drug store and you can easily tell how much this crazy weather is already taking a toll on everyone. Those who have allergy problems can expect them to get ten times worse this year. Those with compromised immune systems like myself can just plan on not leaving your house for the next six months or until the first frost, which ever comes first. Hahahaha! My poor immune system is getting hit hard! It smacked me square in the face once I woke up to a stuffed up nose and sinus headache. Later this afternoon as soon as I stepped outside I quickly returned back to the house to get my trusty mask. No, not Halloween masks although in this city I might as well wear one as nosy folks continue asking, "Whats wrong with you? Why are you wearing a mask?"

Boy! Nevada is sure looking better & better by the day! WHEW!

My friend who has never had allergy problems before just started last year. Today he felt the blunt of it with sneezing, coughing and itchy eyes. He takes sinus medicine but I tend to think there isn't anything strong enough with this crazy weather. I wasn't able to take much of a break from my steroid nasal spray last year. I am now up to taking it twice a day in hopes of staying out of trouble. Maybe I just need to create some masks with sayings on them so it stops people from asking some of the most ridiculous questions. Maybe I just need one word in black marker, "WHAT?" Hahahahaha!

This afternoon I finally had to quit dragging my feet and make an appointment to see my specialist next week regarding the red rash and nagging quad pain-liver/pancreas. Sure, I will always have issues going on with my organs due to my Gastroparesis but if there is anything they can give me to quiet the monster down and put it back to sleep it will be worth the visit! My doctors don't like me procrastinating and waiting until things get out of control. I learned last time when I got a royal ripping over the phone. Its best to work with them as a team, not against them. My spine is still behaving badly today so I wasn't able to do much but at least I was able to get out with my friend for awhile and enjoy the day. Thankfully my post concussion syndrome is now long gone. WOOHOA! One down! If I can continue taking things off my full plate one at a time I will be a very happy gal! Wishful thinking...W I S H F U L thinking...

I got some beautiful red roses today and a very nice card in honor of my GP anniversary from a dear friend. Thank you sooooooooo much! You made my day and brought a huge smile to my face. Its nice to know there are people out there who still treat you as the person you once were before becoming sick. I sure wish they could be a lesson for others. Amen. I have had a few old friends come out the woodwork over the past six months. I like to call them the "Houdini Friends." Those who disappear as quickly as they pop up in and out of your life. Maybe it was a guilty conscience or just curiosity that made them magically appear like nothing happened but a lesson learned as I resort back to watching who I trust. I have had enough hurt in my life and I don't need "Houdini Friends" that come and go when they please. Instead I should take that time and invest it in my real ones. Those who continue accepting me at face value even while being sick. A friend of mine I have known over the past 22 years gave me a few words of wisdom, "If they weren't there for you when things got tough then how in the world can they be there for you now? Look at the once again disappearing act and quit setting yourself up to get hurt." Great advice and once again lesson learned!

"Advice is what we ask for when we already know the answer but wish we didn't."


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: March 21, 2012 2:30 AM EDT
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March 19, 2012
What 'DOES' Work With Gastroparesis?
Mood:  quizzical
Now Playing: Day 703-The Final Road To Survival

It was the dreaded day! Another day dealing with my teeth. Another dentist appointment. UGGG! So far this year I am on 2 dental repairs due to my GP and darn Hell-In-A-Jug treatments literally eating away at the enamel. Thank goodness though that they were able to work me in later this afternoon so that gave me time to catch up on some much needed rest.

2pm and this gal was up with enough time to do the routine wake up chores then head out the door. Always expect the unexpected with GP! Of course instead of just two teeth we quickly found out I have three that need to be repaired. I also have another one on the left side but my dentist understands even I need a break! I think he needs one too because its been nonstop the past two years since going back on treatment. Now that the treatments are weekly it just makes my dental problems ten times worse. I jokingly told him today, "You know you are special because I see you more than I do all my other specialists combined!" Hahahaha! We even have exchanging of jokes while waiting for my mouth to get numb. Yes, hes almost becoming like family now, imagine that! Hahahaha! So after two hours and three teeth later I can now take a short break for a few weeks before heading back so he can repair another tooth and anything else that might be going on. Thank goodness for a break!

We didn't get home until 6pm and not only was my teeth sore but so was my back. Since having spinal problems sitting in the dental chair took its toll. Walking the dogs helped loosen up my back a bit but of course I am sure I will be paying for it later. I have continued the regiment of taking five different types of liquid vitamins and even added two teaspoons daily of a high fruit complex. Honestly to me nothing has yet to work but I keep trying in hopes of one day I can finally see some sort of change. At least its easy to tell what part of the refrigerator is mine. Hahahahaha! I only take up the lower shelf which is enough room for all my liquids. Its literally going to be a Slimfast way of life whether I like it or not. Gatorade has been very hard to consume on a daily basis although I know its important seeing I lose so many electrolytes during my weekly treatments. Gatorade makes me severely nauseated and now since Slimfast changed their formulation I have to literally water down half the bottle. What does work with Gastroparesis I guess is the question?..

My favorite program "The Celebrity Apprentice" was on yesterday and since I already missed one episode I now make sure my DVR player is set. A few of the Gastroparesis Awareness Campaign celebrity supporters are on this season-Dee Snider & Michael Andretti. Dee Snider has been doing a great job staying under the radar although sadly Michael Andretti just got fired off the show two weeks ago. My favorite is Lou Ferrigno! While living with a disability and being bluntly discriminated he still continues to fight on the show proving he is just as capable of doing a great job as anyone else. Yesterdays episode was heart wrenching and ended with him actually winning as the head Project Manager. Just goes to show you should never under estimate the power of the mind and the will to achieve by beating the odds and proving others wrong. Amen!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: March 21, 2012 1:00 AM EDT
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March 18, 2012
Celebrating My GP Anniversary :)
Mood:  special
Now Playing: Day 702-The Final Road To Survival

One thing I always keep in mind each and every day are the words from my Gastroenterologist during my last visit.

"There is no turning back with your Idiopathic Gastroparesis. It will continue progressing. The symptoms will continue getting worse. We can not cure you. There is no medication. Have you accepted this?"

As I woke up today March 18th, 2012 I remembered those exact words and looked at my cell phone calender alarm which read: "MY 8 YEAR GP ANNIVERSARY. KEEP ON! KEEPING ON!" Wow! I made it! I really did make it another year! I have now officially not only beat the initial 4 year projected survival rate for my severe Idiopathic Gastroparesis but I have also doubled it. To some celebrating a terminal condition might sound odd but that's only because those same individuals haven't ever cheated death or know what its like to truly suffer. Amen.

So much has happened over the past 8 years that I don't have enough cyber paper to type it all out on. Hahahahaha! It's been like an old western movie, "The Good. The Bad & The Ugly." Looking back I even sometimes question how the heck I did it?..I could line up about 10 people right now and tell you first hand they sure could never, ever handle what I do on a daily basis as well many other GP'ers. They would had already given up. If you think having the stomach virus or the flu is bad just imagine having those symptoms and more x100 as the condition starts to slowly take over your other organs. Imagine having your life and livelihood instantly taken away and you can't do a darn thing about it. You can only do one thing which is, "ACCEPT IT!"

I got some wonderful cards, emails and text messages this weekend from fellow GP friends and a few others here in the city. Those who I 'thought' would remember sadly didn't but when people try to blame a condition for their lack of heart and compassion its only expected. I have lost and I have gained since being diagnosed with Idiopathic Gastroparesis 8 years ago. I have lost family. I have lost friends. I have lost a spouse. What I have not lost is my pride and will to live. That is something my GP will never, ever take away from me. Today I celebrate 8 years of LIFE. Thank you everyone for your supportive and loving words of encouragement today and through out the years. Gastroparesis has indeed opened my eyes to the world and what it means to care. Kindness comes from those you least expect but in the end you realize who was there for you all along.

Xoxoxoox, Kimberly

"So as you continue your journey remember what I know is true. You'll once again rise on the wings of your soul more graceful, more joyful, more YOU."

Kimberly,

You have done the unthinkable for eight years fighting for your life. You are by far the most inspiring and courageous person I have ever met. Every day you do what a lot of people don't do. You fight and never give up. You not only inspire people to keep on, keeping on but you inspired me to be a better person! You have impacted my life and so many thousands of others around the world that today I wanted to say, "Thank you."

My dear friend,

Good morning and congratulations on persevering and never giving up or giving in by being so strong that I only know you could do. Your friendship over the years has meant so much to me and I don't know what I would do without your humor and uplifting spirit. Always remember you have family all around the world. My door is always open to you and may your beautiful soul always shine. Happy 8th GP Anniversary!


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: March 20, 2012 2:45 AM EDT
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March 17, 2012
Let's Make It A GP-FREE St. Patrick's Day!
Mood:  lucky
Now Playing: Day 701-The Final Road To Survival

It's St. Patrick's & luck of the Irish day!

I woke up with it blazing hot in the living room since the temperatures are still rising outside with a high expected in the low 80's today. Did we ever before celebrate St. Paddy's day in the summer? Yep, we are today! The living room is where I sleep on my couchbed and unfortunately although the direct afternoon sunlight might be great heat for the wintertime it sure isn't for the spring or summer. I had the thermostat set down to 68 degrees and it was cold everywhere else in the house minus the living room. I even had a huge floor fan aimed towards the couches but it was still hot, hot, hot! This darn stomach rash doesn't help nor the upper achy pain either but I guess sooner or later I will learn like everything else with GP which is to just get used to it. At least now I know to gather up all the ice packs in the freezer, wrap them up in towels and place them on the front and back of my abdominal area. It works somewhat to help cool me off a bit but patience is necessary!

Once I finally got some GP relief it wasn't till 3pm by the time I woke up. The animal gang were ready to run in the backyard and take out some of their energy. I didn't see any leprechauns outside nor a pot of gold but I am still alive and that to me is priceless! Amen! I am determined to keep up with the holiday tradition and head out later to celebrate the lucky day. Maybe as well Lady Luck might be on our side since my friend had a few extra greens$$ and wanted to head out to the casino. It takes a bit now to get my body motivated so I wasn't sure by the time I took a shower and got dressed if I would have enough energy to spare for this evening but you only live once and I wasn't going to dare pass up celebrating St. Patrick's day!

By the time we did some chores around the house and took the dogs for a short walk it was already 7:30pm so we got our green on and headed out the door. Since the weather was unusually warm it seemed everyone came out of their winter hiding spots and decided to celebrate the Irish holiday. Not only were the roads crowded but so was the casino. WOW! It was packed!! There were lots of people dressed in green from head to toe and some even dressed as leprechauns, hahahaha! We had lots of fun and although we didn't win a pot of gold it was still nice to get out and celebrate St. Patrick's day! I would be lying if I didn't say it sure felt nice to get home and rest. The fur kids had on their holiday festive attire and greeted us at the front door. They are so used to their Mom being home that now they wait on the couch looking out the window to greet me once I return. That is true dedication! The rest of the evening I decided to have a movie night and RELAX....Cheers to having a great St. Paddy's Day!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: March 19, 2012 3:12 AM EDT
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March 16, 2012
Luck Is In The Air!
Mood:  happy
Now Playing: Day 700-The Final Road To Survival

If this St. Patrick's day weekend turns out anywhere close to the shade of green like the summer-like grass quickly growing outside (due to this crazy weather) then its going to be one LUCKY WEEKEND!

Sadly we found out I am once again building a resistance to my weekly treatments. The reason I had to stop treatments a year ago was due to the exact same reason. Since I am taking the name brand medication the pharmacist suggested I go back to trying the generic. The rash starts within 12 hours after consuming the last glass and goes into two days. I assume that is because it takes my paralyzed organs a few days to even start processing the liquid nightmare. It feels like a horrible sunburn with the chills and sweats. This time the rash broke out on my neck, back and arms. Its happened the past two treatments so now I must be very careful but thankfully the rash did ease up today. Although what I must endure on a weekly basis is not normal its still a must with my unique medical condition.

We are still determined to go out and celebrate the luck of the Irish this weekend but it wasn't going to happen today. There was just way too much going on and the day seemed to fly by! The weather is still bringing us summer like temperatures but it will quickly be coming to an end by later next week. This gal will be more than happy. At least I got a sneak peak of how my body is going to react this spring and summer. Two words: Not good. Better keep my boxing gloves close by for a long fight over the next six months. WHEW!

Later this evening I got some wonderful news regarding the Greyhounds and I am hoping to share it with everyone very, very soon! Indeed it is St. Patrick's Day weekend and may the luck of the Irish also be with you. May it be GP-FREE! CHEERS! 


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
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March 15, 2012
Is It Winter? Spring Or Summer?
Mood:  lazy
Now Playing: Day 699-The Final Road To Survival

I slept horrible! Between the treatment getting stuck inside my intestines, Littleblue bouncing back and forth between the couch and the floor, sweats and the monsoon rain it was a sleepless night. The only positive thing was since the storms produced some serious high winds, hail and lightening most lost their electric. This means my dentist appointment will once again need to be moved to next week. Good news for me because I only got around four hours of sleep and wasn't physically in any way, shape or form capable of dealing with dental work today. Its already been such a hectic week that it might be better to wait things out a few days. I don't have any pain but that's only because of the extensive nerve damage from my GP.

Its not normal to have your heat running one day then your air conditioner turned on the next day but welcome to destroying our ozone layer. Thanks folks! Now we are having record heat while it is still winter. Its not even officially spring yet as the temperatures will continue into the low 80's over the next four days. I already had the sweats last night from treatment so around 4am I got up and turned the air conditioner on. Thank goodness I am not sick 'YET' but I won't push my luck by knocking on any wood either!

My friend has a new project on their hands since buying a large piece of gym equipment last week. The equipment just arrived Monday and since hes being putting it together solo we both realized the directions that say it takes 2-3 hours has now turned into 4-5 hours. Oreo and Pumpkin have been busy playing Supervisor but today its been more like sleeping on the job. Hahahaha! Hes hoping to have it finished by this weekend so my GP room can be back to normal. Gym memberships anymore are so expensive with all sorts of hidden fees that its smarter to buy your own equipment. Its also nice to work out in the privacy of your own home and be able to watch what you like on TV. I sure do miss working out but mostly connecting with people-society. With my spine a mess and dealing with numerous GP problems the best I can do is walk. Its nice having the small park right in front of the house but looks like the rest of the week I might have to just settle for my treadmill. That is if I can catch a break with the Hell-In-A-Jug side effects. By that time I might be due for my next treatment. GEES!!

St. Patrick's day is this weekend and I always try to celebrate. The past four years I had to wait and play things by ear and this time will be no exception. Hopefully by Saturday the rain will ease up a bit and so will my GP-Drano treatment. If not Littleblue promises to be my couchbuddy for the weekend. Hee,hee,hee,hee,hee...


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: March 16, 2012 2:06 AM EDT
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March 14, 2012
Yep! It's That Day Again...
Mood:  don't ask
Now Playing: Day 698-The Final Road To Survival

Here we go again and again and again...

Seems I am far from alone. Many others who have to endure the wicked treatments in order to not become toxic are as well feeling my pain this evening. UGGGG! I like to literally call this treatment, "Treatment From Hell!" Why you may ask? Well because here I am at 11pm and it still has yet to work. My intestines are a mess and seems the past month I am having more problems getting treatment to work that it continues to go into the next 24 hours.

I don't do well thinking about what I am consuming with the toxic poison so I tend to pour my heart and soul into other important issues in life. Helping the Greyhounds is still a work in progress and I am hoping to soon have a positive outcome to this sad story. All in good timing!

My friend has also gotten involved stepping in to speak on my behalf regarding new legislation to put a stop to Ohio Dog Auctions which will stop Puppy Mills. Sad when people lose the meaning of life and treat animals cruelly.

http://www.banohiodogauctions.com/Legislation.html

These are some of the same individuals who lost their brains to the evil eye of the almighty dollar. I believe in the ole saying, "An eye for an eye. A tooth for a tooth." If the bill passes in Ohio it will make it illegal to auction and sell dogs which will put a quick stop to those just like the individuals breeding Greyhounds for money and not providing food, water or proper shelter. Call me one of those individuals that won't give up without a fight! By being AWARE has allowed me to CARE. I might run the Gastroparesis Awareness Campaign but that doesn't mean I don't have other passions in life saving lives, even the furry kind! When you are sick and dying who is always there for you by your side? I know who is for me.

Well this is a short but sweet blog for today. I have Drano still waiting for me and a very long evening ahead! Maybe I need to toss back a few of my friends vitamins after finishing up treatment. Appropriate name for them isn't it?

"ALIVE." Hahahahaha! Mere coincidence? I think not!


Posted by GastroparesisAwarenessCampaignOrg. at 11:00 PM EDT
Updated: March 14, 2012 11:35 PM EDT
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March 13, 2012
Connecting Together With GP Patients :)
Mood:  celebratory
Now Playing: Day 697-The Final Road To Survival

Wow! what a very long and busy day! Might be a good thing keeping my mind busy and off of treatment that must be delayed due to extremely low blood sugar.

Because the weekly treatments are highly dangerous any problems that arise I must hold treatment off for 24 hours because its not worth risking my life. Not that enduring the Hell-In-A-Jug isn't risking your life to begin with...I did my best getting my blood sugar levels up to a safe range but it took until this early evening and by that time forget it! Way too late and I didn't feel like being up all night. The crazy warm weather isn't helping matters. I already miss my snow. Sigh...The flowers are all blooming and the way things are going the grass might need to be cut by next weekend. YIKES! Soon everyone will have their pools open. This might be by next weekend so get your rafts out! I'll bring the Drano. Hahahahaha! Dranotini's for everyone!....

This weekend we are having our first 2012 Gastroparesis Meet and Greet so if you are in the area or can travel we would love to have you join us!

GASTROPARESIS MEET AND GREET 2012

Sunday March 18th

Where: Dave & Buster’s

 Springdale, Ohio

Time: 5pm-?

There will be a group of us getting together for a Gastroparesis Meet and Greet here in Springdale, Ohio March 18-Sunday at 5pm. The location is a restaurant and entertainment center called, “Dave & Buster’s.” The directions and online link are listed below. We would love to have those in the surrounding area join us so please if you are interested stop on by, the more the merrier!  Family, friends and loved ones also welcome. If you plan on coming send us an email so we can get a general idea for table seating J

If you need any further directions you can contact us via email or if you get lost on the way to the restaurant you can contact Kimberly or Jennifer at:

Email-Kimberly/gpawarenessfund@yahoo.com    Cell phone-Kimberly/513-652-6571

Email-Jennifer/jennifer.shumate@gmail.com     Cell phone-Jennifer/336-262-6843

Dave & Buster’s online directions/map to the Springdale/Cincinnati, Ohio location:

http://www.daveandbusters.com/Locations/Default.aspx?search=45246

11775 Commons Drive, Springdale, Ohio 45246 /513-671-5503

We look forward to meeting everyone and please don’t forget to bring your cameras! J

Kimberly, Jennifer and Melissa


Posted by GastroparesisAwarenessCampaignOrg. at 11:58 PM EDT
Updated: March 14, 2012 2:21 AM EDT
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