It's funny how different medications work differently for different people and different age groups. My 8 year old daughter recently had versed before a minor throat surgery and you should have heard her! She was giggling and singing random things (extremely loudly). She was also hallucinating. I've never seen anything like it. When they wheeled her down the hall she was screaming "WHEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEE THIS IS A FUN RIDE!!!" It was pretty funny.
Finally just had my PEG tube surgery today. I have been in the most pain from it I think I have ever been in my life. And no pain meds for home. Still scared to use it until the nurse comes tomorrow. I am still so grateful and thankful for the PEG and the fact I don’t have a tube on my face anymore after over 2 years. #worththepain !!!
I'm happy you found a system for your pain management that works for you I like that you show the real you and don't play to the camera. It's your genuineness that makes me love your channel. Please never change who you are.
I love it when you’re loopy!!! I’m having Botox injections in my stomach for gastroperisis on Friday morning. It’s kinda like an endoscopy and I’ll be put under. It really helps me to not feel nauseous or have vomiting. I’ve had it done in August and its been six months and really helps.
I go next week for injections and I have found the more I get them the more nervous I am. I have horrible anxiety and it gets worse each time. I'm so hopeful this round of injections work. I just want to not be in so much pain all the time. Thank you for your videos they mean so much to me.
Just had my first ketamine infusion treatment, and I was awake for most of time. Slept about 30 mins of 4 hrs of infusion. Like you, I don't like the loopy out of control ride ketamine sends you on. Definitely not fun, but the relief has been mild so far. Thinking I'll be asking for something to knock me out, and the versed at the end...might make the experience better for me too...yes the toradol was helpful too
#NoPain #NoLoopiness. I am glad that you feel much better coming out of the procedure. Even thought it is funny the things you say, you also have a lot of anxiety (Where is Harlow? Where is my cow? My feet are running away). So you feeling better after the procedure is great, and I am glad that you are taking the treatments well.
I'm with you on that one, Jaquie. I have had over 50 surgeries and I still cry like a baby just before they have to put me under. Not saying you cry like a baby but the feeling nervous thing. Its not fun. I love how positive you are about all your trials. I definitely admire you more than I could ever tell you.
I had a win with my Dr today. I felt that this time he really listened to me about my pain. We are now increasing my Norspan patch dose & I will have Endone for my breakthrough pain. As you said today, we learn to adapt with our pain but there are days you just need more pain relief to help you get through it. So glad you had a better post op effect, I wonder if it will make the recovery days better too? My Dr wants me to have more joint injections & I want to suggest we try the Toridol (did I spell that correctly?) but I’m not sure if it’s used here in Australia. Fingers crossed.
Jaquie, I'm really pleased that your pain management team was able to make an adjustment to your operative medications that gives you more comfort and peace when you wake up. I'd love an update on how you are doing with the CBD oil. Wishing you, Judd, and Harlow the best always.
When I was a paramedic our ER made it a point to use Versed to help people forget their horrible traumas. But it does not erase my memory. I'm so glad you speak up for yourself. And I'm so happy you feel better. It truly gladens my heart.
Hi Jaquie, your positivity is incredible. I was just diagnosted with POTS and Gastroparesis. I also have CVS. I am struggling with being positive and coping with my diagnosis. I was wondering if you have any tips on being positive and pushing forward.
I have a video called "Staying Positive with Chronic Illness" that you might like! (: Also a "Chronic Illness Support" playlist. Hang in there, you are not alone
I have gastroparisis as well . It sucks . I am getting a procedure done on the 9th to see if it’ll help food pass easier rather than sitting in my stomach and guts and causing pain
I’m not gonna lie, I’ve been watching your videos for awhile now and I don’t remember how I found your videos but I wouldn’t of known anything about chronic illnesses if it wasn’t for you. 😊 Getting more and more informed, thank you! 💕
I'm glad that you had a better experience this time. Sharing your experiences is not always easy to do but you do it. Thank you for sharing I truly appreciate it.
I’m just glad that they found something to make your procedures work better for you! I hope they fix up the electricity issue ASAP and that the remote start, gets to working.
I'm so glad that you had a better experience waking up from anesthesia! 100% you don't have any apologize owed to your viewers for taking the extra versed. The aim of your journey is to manage your pain and conditions so that you can live your life with the best quality possible. Waking up more peacefully is just another piece of that very complicated puzzle.
Good morning Jaquie, back at the operation again, good luck and keep resting. My operation is next month and thank you for your advice on getting my leg braces. God Bless!
I laughed so hard when you blamed the urn for your electrical problems. Also, it's great to see you feeling so good after each of your pain management procedures. There is always such a big change. I'm happy that it is working out well for you!
Jaquie, I have a question, what type of tests did you have to do to find out you had POTS and EDS ? And what were your symtoms to make your doctor decide to give you the tests? I ask becasue I find that pain pills dont really work for me, and then every ER doctor tells me that thru the vein the pain meds work better, but I find that thru my muscle they work better for me, Ive tried to tell the ER staff that, but I just get ignored . Connecticut is a terrible place to find doctors especially pain doctors, I had a GB who was a petatrican, who managed my pain, but he woudnt allow the PORT, now I dont have him, and I have the Port, but the last pain doctor I went too, basically wasnt really a doctor she was like APRN, type of thing, who basically just yelled at me for the amount of Dilaudid I was taking, and I was moved from 20mg every 4 to 4mg every 6 so Im hurting, ALOT !!! But I dont have the abiliy to go far out of town. SO it takes more for my body, if they arent using shots into my arms same as my iv pain meds when Im in the hospital. I also dont want to go back to that pain management if im gonna be screamed at even beore meeting the doctor!! Just curious ... Thanks... Kimberley
I'm not as educated in eds because I don't have it but I have POTS. POTS has to do with your heart rate and blood pressure it causes dizziness and passing out mainly along with other things that are involuntary functions. EDS I believe is what you want to check into because like Jacquie was saying her body was processing meds fast but I might be wrong and it's another illness. EDS is hypermobility. People deal with subluction, joints popping out, people with ports that aren't accessed all the time their ports can flip (I have a friend dealing with this right now) you can Google eds and look at pict that are a base line idea if you have it due to different body positions you can do
I appreciate that you guys share your life! I understand that you’re just living your life and that you don’t do things for the sake of vlogging! Take care! Sending love.
In my family we metabolize painkillers quickly, so morphine, tramadol, vicodin, etc. doesn't touch our pain. Novocaine and lidocaine don't work for my older sister, so she has to use septacaine. So I'm glad you found a dose to ease the loopiness! Even though it's hilarious to see, I understand wanting to be in control and not wanting to be bothersome if you were to be too vocal. Even if you're feeling better you should stick to your schedule with using the AFOs so when the pain management wears off you haven't overdone it with the AFOs and suffer the consequences!
I love the 3 of you!!…Jaquie please never feel the need to do something that you feel/know in your heart is not good for your health just to “entertain” people!!
Seeing your post procedure attitude being so incredibly positive was great! 😁 It seems you were even more animated than usual. Glad it was so positive!
I’m on a waiting list for an operation to remove cystic tissue that was left behind in an operation I had in 2005, the doctor is waiting for the government to approve the operation and then I have all the paperwork at work for the time off to ask for.
We totally understand that you don’t enjoy being loopy when you wake up!! Losing control is a scary thing so I’m so happy that you found a way to limit the loopiness ❤️ and I’m looking forward to that fun compilation 😂😂
You need to replace a fuse in your breaker box more than likely. Call an electrician or your maintenance for your building. It's usually not a big deal but it could start a fire.
I suspect it's compensatory muscle movements i have to make in the car to stop from being thrown around that can lead to more pain and fatigue. I also struggle with that with my EDS, it could be a similar cause for you jaquie. I think we don't realize how much our muscles have to engage when we go around corners and brake etc. Sometimes i have to recline fully in the car because i become too faint to not get shaken around. I feel more vulnerable when i can't see out the window though so i don't do it often
Your vlog made me happy (Ik that’s weird lmao) I’ve had a rough day in school. I have so many assignments and I have the SAT next weekend (which is a 4 hour test). I was getting so frustrated with some of the SAT studying so I started crying bc I was so stressed and frustrated but your vlog made me feel better (if that makes sense) anywho I hope you have a good day :)
Everyone asking why the couch is plugged in.. it's an electric couch that is controlled by a button to raise and lower the recliner part. It has to be plugged in to work.
Yeah those loopy things you say are hilarious, but I understand. I have friend hwo sometimes just falls and might be having convulses and she of course have no idea how long she has been fainted and so. I get it, it dosent feel nice when things you do are out of your own control :(
Ok so here's my 2 cents about the ketamine loopiness. Yes, it is somewhat hilarious what happens when you come out of your sedation but you are right, you shouldn't have to go out of your way to make us watch your vlogs. I totally support what you are doing, I watch because you inspire me to do better and be better not because of some hilarious antics but because you aren't afraid to show the world what the life of a spoonie is really like. If a chronic warrior such as yourself and Janeice from The Raw Life can get out of bed everyday and face the world then so can I. Keep doing what you are doing and never change!! Love you darlin' and #keepmoviningforward
I talked to my doctors and sadly I can't get ketamine at all for my pain. I'm so glad you're able to get pain relief. Thank you for sharing all of you journey with us.
Sorry to hear that :( Not many doctors know about Ketamine, I did not know about it. I was thankful my doctor was using it already on patients when I saw him and he thought it would help me.
The only thing I missed from the extra Versed, was even a tiny little, "No Pain!!!" I totally understand the need to control as much as possible. I think it's both an autism thing, and a chronically ill thing. (Incase I never mentioned it, also it would be pretty arrogant of me to assume you'd remember, I was diagnosed with Aspergers an an adult, before it was stricken from the diagnostics. My daughter is also an Aspie Girlie.) I don't have EDS, but because I am a big girl and because I have been on opioids for a very long time, I also am able to converse so cogently with drugs in my system. My last major surgery, I had a low blood pressure episode during the surgery. My recovery nurse (and they had one nurse for every TWO BEDS!!! I HAVE NEVER SEEN THE LIKE BEFORE IN MY LIFE!!!) thought I was a nurse myself or at the least a med student (University of Michigan is a teaching hospital) because I was so knowledgeable and lucid. I've also woken up in the middle of procedures because the nurses at the procedure centers didn't listen to my doctor (My first GI, Dr. Marvelous...he also saved my life, but that is another story) and failed to give me sufficient drugs to keep me under. The same nurses ignored me when I gave them important information about how to set an IV for me. I no longer have procedures in surgery centers. My current GI, Dr. Awesome, (Dr. Marvelous retired several years ago) forbids it. (I don't have bad veins, but they are wise to sticks and tend to duck and roll even when you think you have them. My skin, while not leather-like, is tougher than it looks, so you have to push harder than you think you do, and when you're having a colonoscopy done, you're automatically dehydrated to start with! At the time, I was getting Remicaid every 4 weeks, so at least one IV per month.)
I have a jaw surgery coming up, and I am requesting ketamine. I really hope they can do that. I'm really worried about the pain . I appreciate that you are sharing your journey! It has helped me in so many ways!
Do you have those outlets that have the test/reset buttons on it? Sometimes in my house one of the outlets will pop and take out a electrical line. Flipping the breakers won't help, but pushing the button on the outlet will fix it.
That great that they were able to control the loopiness and u werr able to wake up peacefully. I think u should get the surge protecter power strip if u have so many things to plug it. Maybe that will fix the issue with ge lights turning it off byitself.
Hey jaquie! I’m having a POP procedure on the 9th. Have you ever heard of it or had it done ? “minimally invasive endoscopy therapy, per oral endoscopic pyloromyotomy (POP)”
The loopiness people get actually kind of scares me. Watching you go through that in the past has eased my mind a little, knowing this is normal and it wears off. I do prefer the peaceful grogginess over the loopiness. Either way, I am glad things went well for you.
I think you passed the electrical curse to meee! lol. My upstairs lights won't work ahh. I've only ever been put out with propofol. It just makes me sleepy afterwords. When you wake up from ketamine, do you remember the loopy parts?
Not really it is mostly a hazy, faint recollection. Kind of like a dream but I can sort of recall the state I was in... But I also have gaps in my memory, like some parts of pre-op before I even got the Ketamine. It is weird.
My mother is loopy after surgery. The anesthesiologist suggested to increase her oxygen post surgery and it helps with the loopy feeling. Wonder if that would help you?
It's funny how different medications work differently for different people and different age groups. My 8 year old daughter recently had versed before a minor throat surgery and you should have heard her! She was giggling and singing random things (extremely loudly). She was also hallucinating. I've never seen anything like it. When they wheeled her down the hall she was screaming "WHEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEEE THIS IS A FUN RIDE!!!" It was pretty funny.
Actually, I missed your loopiness !! Glad you're responding better to the treatments everyday !
I’m so glad you had a better experience than normal with your anesthesia!
My best wishes for you on Rare Disease Day! 💜💜💜🦓🦓🦓
Finally just had my PEG tube surgery today. I have been in the most pain from it I think I have ever been in my life. And no pain meds for home. Still scared to use it until the nurse comes tomorrow. I am still so grateful and thankful for the PEG and the fact I don’t have a tube on my face anymore after over 2 years. #worththepain !!!
I'm happy you found a system for your pain management that works for you I like that you show the real you and don't play to the camera. It's your genuineness that makes me love your channel. Please never change who you are.
you and Judd are to cute together you two bring out the kid in each other lol.
I love it when you’re loopy!!! I’m having Botox injections in my stomach for gastroperisis on Friday morning. It’s kinda like an endoscopy and I’ll be put under. It really helps me to not feel nauseous or have vomiting. I’ve had it done in August and its been six months and really helps.
I go next week for injections and I have found the more I get them the more nervous I am. I have horrible anxiety and it gets worse each time. I'm so hopeful this round of injections work. I just want to not be in so much pain all the time. Thank you for your videos they mean so much to me.
Just had my first ketamine infusion treatment, and I was awake for most of time. Slept about 30 mins of 4 hrs of infusion. Like you, I don't like the loopy out of control ride ketamine sends you on. Definitely not fun, but the relief has been mild so far. Thinking I'll be asking for something to knock me out, and the versed at the end...might make the experience better for me too...yes the toradol was helpful too
#NoPain #NoLoopiness. I am glad that you feel much better coming out of the procedure. Even thought it is funny the things you say, you also have a lot of anxiety (Where is Harlow? Where is my cow? My feet are running away). So you feeling better after the procedure is great, and I am glad that you are taking the treatments well.
I'm with you on that one, Jaquie. I have had over 50 surgeries and I still cry like a baby just before they have to put me under. Not saying you cry like a baby but the feeling nervous thing. Its not fun. I love how positive you are about all your trials. I definitely admire you more than I could ever tell you.
I do enjoy the loopiness however I'm happy that you were more at peace this time waking up. I'll excited for the compilation video!
I had a win with my Dr today. I felt that this time he really listened to me about my pain.
We are now increasing my Norspan patch dose & I will have Endone for my breakthrough pain. As you said today, we learn to adapt with our pain but there are days you just need more pain relief to help you get through it.
So glad you had a better post op effect, I wonder if it will make the recovery days better too?
My Dr wants me to have more joint injections & I want to suggest we try the Toridol (did I spell that correctly?) but I’m not sure if it’s used here in Australia. Fingers crossed.
So glad things went well! Over here I have seen it spelled Toradol, it may be worth asking about! Can't hurt to mention it (:
Chronically Jaquie , Thanks for the spelling, it def can’t hurt to enquire about it.
Jaquie, I'm really pleased that your pain management team was able to make an adjustment to your operative medications that gives you more comfort and peace when you wake up. I'd love an update on how you are doing with the CBD oil. Wishing you, Judd, and Harlow the best always.
When I was a paramedic our ER made it a point to use Versed to help people forget their horrible traumas. But it does not erase my memory. I'm so glad you speak up for yourself. And I'm so happy you feel better. It truly gladens my heart.
I have had 42 surgeries and I am 30 years old. I still get nervous before any procedure or surgery. You are not alone Jaquie and been praying for you.
It might be a circuit on your neighbors electrical if you do have an apartment next to you they sometimes wire them that way
Light problems only mean one thing: STRANGER THINGS!
Hi Jaquie, your positivity is incredible. I was just diagnosted with POTS and Gastroparesis. I also have CVS. I am struggling with being positive and coping with my diagnosis. I was wondering if you have any tips on being positive and pushing forward.
I have a video called "Staying Positive with Chronic Illness" that you might like! (: Also a "Chronic Illness Support" playlist. Hang in there, you are not alone
I have gastroparisis as well . It sucks . I am getting a procedure done on the 9th to see if it’ll help food pass easier rather than sitting in my stomach and guts and causing pain
Chronically Jaquie Thank you so much, I will surely check those out.
Anyone else going back through all the Ketamine injection videos for all the lolz? Jaquie always made me smile 😅
That face at 8:14 is just too precious! I'm glad your pain management treatment went so well!
I’m not gonna lie, I’ve been watching your videos for awhile now and I don’t remember how I found your videos but I wouldn’t of known anything about chronic illnesses if it wasn’t for you. 😊 Getting more and more informed, thank you! 💕
Can you ask your seamstress to make a lining/scarf to prevent irritation from the brace?
I'm glad that you had a better experience this time. Sharing your experiences is not always easy to do but you do it. Thank you for sharing I truly appreciate it.
Hello Jacquie and Judd, I hope everything works out for you. Sending love prayers and support. You are awesome and a warrior. 😘💞
Things will get better for you. Lots of love and prayers for you all.
So glad that your pain management plan is even better now (without the loopiness)! Hope you're getting some relief :)
I’m just glad that they found something to make your procedures work better for you! I hope they fix up the electricity issue ASAP and that the remote start, gets to working.
I'm glad that you found a way to prevent the loopyness! It's funny to watch but it can't be fun to go though
I'm so glad that you had a better experience waking up from anesthesia! 100% you don't have any apologize owed to your viewers for taking the extra versed.
The aim of your journey is to manage your pain and conditions so that you can live your life with the best quality possible. Waking up more peacefully is just another piece of that very complicated puzzle.
Good morning Jaquie, back at the operation again, good luck and keep resting. My operation is next month and thank you for your advice on getting my leg braces. God Bless!
I laughed so hard when you blamed the urn for your electrical problems. Also, it's great to see you feeling so good after each of your pain management procedures. There is always such a big change. I'm happy that it is working out well for you!
Jaquie, I have a question, what type of tests did you have to do to find out you had POTS and EDS ? And what were your symtoms to make your doctor decide to give you the tests? I ask becasue I find that pain pills dont really work for me, and then every ER doctor tells me that thru the vein the pain meds work better, but I find that thru my muscle they work better for me, Ive tried to tell the ER staff that, but I just get ignored . Connecticut is a terrible place to find doctors especially pain doctors, I had a GB who was a petatrican, who managed my pain, but he woudnt allow the PORT, now I dont have him, and I have the Port, but the last pain doctor I went too, basically wasnt really a doctor she was like APRN, type of thing, who basically just yelled at me for the amount of Dilaudid I was taking, and I was moved from 20mg every 4 to 4mg every 6 so Im hurting, ALOT !!! But I dont have the abiliy to go far out of town. SO it takes more for my body, if they arent using shots into my arms same as my iv pain meds when Im in the hospital. I also dont want to go back to that pain management if im gonna be screamed at even beore meeting the doctor!! Just curious ... Thanks... Kimberley
I'm not as educated in eds because I don't have it but I have POTS. POTS has to do with your heart rate and blood pressure it causes dizziness and passing out mainly along with other things that are involuntary functions. EDS I believe is what you want to check into because like Jacquie was saying her body was processing meds fast but I might be wrong and it's another illness. EDS is hypermobility. People deal with subluction, joints popping out, people with ports that aren't accessed all the time their ports can flip (I have a friend dealing with this right now) you can Google eds and look at pict that are a base line idea if you have it due to different body positions you can do
I appreciate that you guys share your life! I understand that you’re just living your life and that you don’t do things for the sake of vlogging! Take care! Sending love.
I hate feeling out of control so I completely understand. I'm really glad you were able to find a dosage that helps. :)
In my family we metabolize painkillers quickly, so morphine, tramadol, vicodin, etc. doesn't touch our pain. Novocaine and lidocaine don't work for my older sister, so she has to use septacaine. So I'm glad you found a dose to ease the loopiness! Even though it's hilarious to see, I understand wanting to be in control and not wanting to be bothersome if you were to be too vocal. Even if you're feeling better you should stick to your schedule with using the AFOs so when the pain management wears off you haven't overdone it with the AFOs and suffer the consequences!
I love the 3 of you!!…Jaquie please never feel the need to do something that you feel/know in your heart is not good for your health just to “entertain” people!!
i feel like i get just as many smiles from normal videos as i did from past loopyness
Seeing your post procedure attitude being so incredibly positive was great! 😁 It seems you were even more animated than usual. Glad it was so positive!
Jaquie you are my inspiration to keep fighting on these battles 🌼
I’m on a waiting list for an operation to remove cystic tissue that was left behind in an operation I had in 2005, the doctor is waiting for the government to approve the operation and then I have all the paperwork at work for the time off to ask for.
We totally understand that you don’t enjoy being loopy when you wake up!! Losing control is a scary thing so I’m so happy that you found a way to limit the loopiness ❤️ and I’m looking forward to that fun compilation 😂😂
i liked seeing u wake up on a more controlled state its peaceful and i get the need for control thing
You need to replace a fuse in your breaker box more than likely. Call an electrician or your maintenance for your building. It's usually not a big deal but it could start a fire.
I suspect it's compensatory muscle movements i have to make in the car to stop from being thrown around that can lead to more pain and fatigue. I also struggle with that with my EDS, it could be a similar cause for you jaquie. I think we don't realize how much our muscles have to engage when we go around corners and brake etc. Sometimes i have to recline fully in the car because i become too faint to not get shaken around. I feel more vulnerable when i can't see out the window though so i don't do it often
Hey jaquie and I love that you are open and honest with us
Jaquie you're amazing warrior w your pain management 😊❤️💚💚💪🏻💪🏻
I love to see you smile.
This time you didn't scream NO PAIN 😂
delfin wasser yep
Your vlog made me happy (Ik that’s weird lmao) I’ve had a rough day in school. I have so many assignments and I have the SAT next weekend (which is a 4 hour test). I was getting so frustrated with some of the SAT studying so I started crying bc I was so stressed and frustrated but your vlog made me feel better (if that makes sense) anywho I hope you have a good day :)
We have remote start on my mom's car and it has not worked more times then it has worked.
Everyone asking why the couch is plugged in.. it's an electric couch that is controlled by a button to raise and lower the recliner part. It has to be plugged in to work.
I am glad to hear that you are feeling better and you are right that we are all different with meds may god bless you and your family💙💕💙💕💙💕
I still think pain management procedure is a mouthful😂 how about PMP just a suggestion
Yeah those loopy things you say are hilarious, but I understand. I have friend hwo sometimes just falls and might be having convulses and she of course have no idea how long she has been fainted and so. I get it, it dosent feel nice when things you do are out of your own control :(
That outlet is like the National lampoon's Christmas vacation one where everything was plugged into one outlet.😂😂😂😂
I love watching jaquie waking up it’s so funny!!!
Ok so here's my 2 cents about the ketamine loopiness. Yes, it is somewhat hilarious what happens when you come out of your sedation but you are right, you shouldn't have to go out of your way to make us watch your vlogs. I totally support what you are doing, I watch because you inspire me to do better and be better not because of some hilarious antics but because you aren't afraid to show the world what the life of a spoonie is really like. If a chronic warrior such as yourself and Janeice from The Raw Life can get out of bed everyday and face the world then so can I. Keep doing what you are doing and never change!! Love you darlin' and #keepmoviningforward
Thumbs up for Harlow nose art lol!
Judd wouldn't like my electrical outlets either...All of them are packed with plugs! I am also a fire hazard, waiting to happen, lol!
You both are so funny together love it so happy that your thing went well today 😍😍😍👍🏻👍🏻👍🏻
What type of back pack is this in the video when you are sitting on the couch? Love it! - Holly
I talked to my doctors and sadly I can't get ketamine at all for my pain. I'm so glad you're able to get pain relief. Thank you for sharing all of you journey with us.
Sorry to hear that :( Not many doctors know about Ketamine, I did not know about it. I was thankful my doctor was using it already on patients when I saw him and he thought it would help me.
Sometimes the remote start requires you leaving the key in the car to have it actually start
Hi Jacquie, you go through so much everyday. God bless you. You are always in my prayers.
For your electrical problem maybe you could use a heavy duty power strip.
You guy's are SO ADORABLE!!!!!!!
HI I got a 9 week old puppy on Sat she is part st benard part Akita I'm so busy and happy she's going to be my mobility service dog
My vision is being weird today. I thought the title on the picture said ketamine infection instead of ketamine injection. I was very confused.
Aw I miss singy, happy Jacquie. So many great laughs 😂
The only thing I missed from the extra Versed, was even a tiny little, "No Pain!!!"
I totally understand the need to control as much as possible. I think it's both an autism thing, and a chronically ill thing. (Incase I never mentioned it, also it would be pretty arrogant of me to assume you'd remember, I was diagnosed with Aspergers an an adult, before it was stricken from the diagnostics. My daughter is also an Aspie Girlie.)
I don't have EDS, but because I am a big girl and because I have been on opioids for a very long time, I also am able to converse so cogently with drugs in my system.
My last major surgery, I had a low blood pressure episode during the surgery. My recovery nurse (and they had one nurse for every TWO BEDS!!! I HAVE NEVER SEEN THE LIKE BEFORE IN MY LIFE!!!) thought I was a nurse myself or at the least a med student (University of Michigan is a teaching hospital) because I was so knowledgeable and lucid.
I've also woken up in the middle of procedures because the nurses at the procedure centers didn't listen to my doctor (My first GI, Dr. Marvelous...he also saved my life, but that is another story) and failed to give me sufficient drugs to keep me under. The same nurses ignored me when I gave them important information about how to set an IV for me.
I no longer have procedures in surgery centers. My current GI, Dr. Awesome, (Dr. Marvelous retired several years ago) forbids it.
(I don't have bad veins, but they are wise to sticks and tend to duck and roll even when you think you have them. My skin, while not leather-like, is tougher than it looks, so you have to push harder than you think you do, and when you're having a colonoscopy done, you're automatically dehydrated to start with! At the time, I was getting Remicaid every 4 weeks, so at least one IV per month.)
we all enjoy the loopy Jacquie! God bless
Return of "work what finds for you" 😂😂
I have a jaw surgery coming up, and I am requesting ketamine. I really hope they can do that. I'm really worried about the pain . I appreciate that you are sharing your journey! It has helped me in so many ways!
My remote start is finicky too!!
Silly Judd, she is Mrs. Beckwith (sp?) not Ms. Blake!!
Do you have those outlets that have the test/reset buttons on it? Sometimes in my house one of the outlets will pop and take out a electrical line. Flipping the breakers won't help, but pushing the button on the outlet will fix it.
That great that they were able to control the loopiness and u werr able to wake up peacefully.
I think u should get the surge protecter power strip if u have so many things to plug it. Maybe that will fix the issue with ge lights turning it off byitself.
Glad the procedure went well and I hope Ford we’re able to unjinx the car too!
8:20 When something (maybe a manatee??) touches your foot in the water
That was a much better way for you to way up =3 i'm glad you guys figured it out!!!
Hey jaquie! I’m having a POP procedure on the 9th. Have you ever heard of it or had it done ?
“minimally invasive endoscopy therapy, per oral endoscopic pyloromyotomy (POP)”
The loopiness people get actually kind of scares me. Watching you go through that in the past has eased my mind a little, knowing this is normal and it wears off. I do prefer the peaceful grogginess over the loopiness. Either way, I am glad things went well for you.
I would call the landlord or maintenance people. It sounds like the internal wireing needs to be looked at.
God bless you and jedd. I love your Harlow. Glad everything went good.❣️❣️❣️❣️👍
youre eyes at 8:22 😂😂😂
The loopiness is just a added advantage. Your vlogs are entertaining and informative without them too. Glad you had a better experience.
Hope everything will do good today for you juqie
that face!!!!!!!!! that was soooo funny!!
I might as my pain management doctor about this particular treatment.
I’m going to Pain Management tomorrow I hope she can do something for my muscles. The shots didn’t help last time.
Best of luck!
Try a power strip instead of the outlet extenders?
I think you passed the electrical curse to meee! lol. My upstairs lights won't work ahh.
I've only ever been put out with propofol. It just makes me sleepy afterwords. When you wake up from ketamine, do you remember the loopy parts?
Not really it is mostly a hazy, faint recollection. Kind of like a dream but I can sort of recall the state I was in... But I also have gaps in my memory, like some parts of pre-op before I even got the Ketamine. It is weird.
And, it also depends on the infusion. Each time is different!
you need to get plug where you can plug in many things
lol it was funny when you were loopy so the car auto start doesnt work?
My mother is loopy after surgery. The anesthesiologist suggested to increase her oxygen post surgery and it helps with the loopy feeling. Wonder if that would help you?
Really really quick at 7:34 .... there's a man's voice in the background. Kind of reminds me of the haunted mansion voice over.... lol
I'm glad the extra Versad worked and that you woke up peacefully. It is about figuring out what works for you. Thanks for showing us your journey.
Why does your couch need to be plugged in to the electricity?
Try double locking then holding the lock button :)