วีดีโอ

Usually affects humans at birth and is called (obstructed birth) obstructed childbirth is the narrowing of the vagina in a woman and the impact of the fetal brain with the female pelvis at birth and must immediately turn the natural birth to a caesarean section after a maximum of two hours in order not to occur bleeding in the fetus and this leads to bleeding in the brain of the fetus and thus lack of oxygen in the child and cerebral palsy accompanies the child throughout his life and becomes unable to eat through the mouth

@@chandraneepurhooa5418thank you! Yes, I still have my GJ feedube tube and rely on it for 95+% of my nutrition, water, and some meds

I'm confused

No, I need Ollie. Ollie isn't there just because I felt like it. He is a (multipurpose, but mainly a) medical and cardiac alert Service Dog that cannot be replaced by any medical equipment. There currently isn't any medical equipment that comes close to what Ollie does. Under the ADA, Service Dogs are considered “medical equipment”. So, just as I have the right to bring a wheelchair, feeding tube, oxygen tank, etc., I have the right to have Ollie with me. That's why it's really important for him to be groomed often (2x a month), always wiping his paws down to keep them clean if he's not wearing his booties, get frequent checkups with his vet, and that he's up to date on all his vaccinations. You are far more likely to sick from another human than a Service Dog that meets all the requirements. He doesn't come in contact with any food so there's nothing to worry about there. I agree that not every Service Dig handler follows the requirements, but they are the exception, not the rule. They should not affect my rights as a disabled Service Dog handler. Please look up ADA.GOV if you want more information. I'll comment the link that focuses on Service Dogs. I hope that answered your question.

The general ADA link with common questions about Service Dogs www.ada.gov/resources/service-animals-faqs/ And Q. 10 is actually the law about open salad bars, since that may answer your question the closest. Q. 32 talks about restaurants and how they are allowed to be accompanied by their handler but how they are not allowed to sit on the chairs for concerns just like yours. This is all under the ADA (Americans with Disabilities Act) and there's what it says on that same link “The Americans with Disabilities Act authorizes the Department of Justice (the Department) to provide technical assistance to individuals and entities that have rights or responsibilities under the Act.” I hope this all answers your questions and/or concerns.

@@michelewhite1900s This isn't my audio (as mentioned in the pinned comment and description). Unfortunately, just because you haven't experienced need it, doesn't mean others haven't. To share my own experience with SSI, even though I'm not married- I have SSI and it would be altered if I got married. As an example, I live at home with my parents and I couldn't afford to pay them rent like I wanted to (and I would if I got the money from SSI to help pay for my part of the bills). But because my “household income” is a certain amount, I get significantly less. I am unable to even pay for all of my medications, copays (even with absencindary insurance), feeding tube supplies, and other medical supplies, contributing toward household bills, let alone rent. I have to notify them immediately if I get married or my living situation changes. So, it is true that someone's “household” income could affect their SSI and some of it could be “taken away” if their marriage status changes. I know of multiple couples who continue life as if they are married but have chosen to get a divorce on paper so they can increase their SSI to be able to afford basic living and medical expenses. They have also always had separate bank accounts because if you have over $2,000 you will not get any income that month (which happened to me after my grandpa wrote me a check to pay for classes at my local JC and I had about $2,050 and I couldn't afford medications that month). The point is that the system is messed up and there is a lot of room for improvement. I recognize that I'm incredibly fortunate to have the support of my family. The majority of people in my situation are not as lucky. I'm very grateful for the support that I have. I don't know what to do without them. I am not super knowledgeable about how all the systems work, but this is my personal experience.

@@snuggies8037 I'm so so sorry you have gone through that! My heart goes out to you!! 🤍

@@alliegunderson544 awe! I love knowing Ollie has so many twins out there! 💚🐾

Actually, Ollie is a goldendoodle but he looks just like a SP. Most people asssue he is a SP, or at least until they see his tail. 🐕‍🦺

@@thatonepossum5766 this is very true. I’m so sorry that happened to you!

@@Chronically.sarahdayton luckily it hasn’t happened yet, it’s just something I’m aware of and cautious about.

@@stormyeffects4795 thank you 💚

@@michellecolegrove I'm sorry that someone made you feel so awful. I wish I could say it got better but it doesn't. I have learned how to respond to people, if I do at all. A lot of it is misinformation or ignorance. Regarding the harnesses, it really depends on they type of work they do. Because Ollie does mobility, he has to wear a harness that is safe. Unfortunately, The company that made Ollie’s everyday harness I use now is no longer in business. I am actually waiting on a new one from Misty’s Dog Gear (on IG). I bought an x back this time (his current one is a Y front). If you don't need mobility, you may not need a harness. You could just get straight front vests for labeling reasons. Ollie’s cape is custom and it's from PatienceAndLove143 on Etsy and I love it. I also use the One Tigris vest as a cape with patches and I like that as well for days I don't need mobility or extra bulk (like the airport). I also use it around holidays (like Christmas)!because I have specific patches that I love to theme out but you could do it that way and have a few sets of patches to swap out bc it's a lot of fun and it makes it special. I have used Bridgeport harness before during his training, and I liked that a lot but I prefer biothane over leather. Idk if this is helpful. It truly depends on what you need. I have a full gear tour on my channel. It's linked in the description and it's the most viewed video on my channel so it should be easy to find. I hope that helps. 💚

@@Behind-the-ears4_4 I couldn't agree more!

@@Chronically.sarahdaytonwonder if there is a way to report them

@@Waff._Z It's something known as imposter syndrome. I've personally struggled with it as long as I've been “sick”. I know how hard it can be to struggle with that and the constant second guessing yourself. It's tricky. I still struggle with it now, even though I'm dependent on a feeding tube, and my port for infusions, take over 2 dozen medications, have a Service Dog, unable to live on my own, am in need of a liver transplant, etc. I hope that you learn from me and be more kind to yourself. And most of all, know that *you are valid*. 💚

​@@Chronically.sarahdayton I'm sorry i didn't see this for so long but ty for taking the time to talk to me ❤

Yes agreed. I have symptoms of ADHD but I always wonder if I’m not “disabled” enough to seek diagnosis.

@@1313fidel 💚💚💚

Thank you! Sorry, I'm not sure I understand. 😅 What do you mean by profiles?

@@Chronically.sarahdayton profile pictures, sorry I'm not good with english.

@@colorfulphoenix23 no worries! I have dyslexia, so I'm not good at it either lol. Do you mean like the one with the pride flag in the profile picture? I just updated mine. I also just made a community post using that so you can let me know if that's what you mean. Is it that what you mean or do you mean sharing other people’s accounts? It’s hard to explain so I hope you understand what I’m trying to say 😅

@@jessicalingo4346 I completely agree. A lot of people don’t see it that way and tend to misinterpret my view of it. I’m glad someone else designated with this. 💚

@@Chronically.sarahdayton I commented on the fact that service animals are considered medical equipment in some areas but not in others on another post and I was so excited I wasn't the first to say that. I do hope that changes in the future. Unfortunately I can see it being a money trap since insurance companies are a beast with common required medications. So in some ways I'm happy they're not because of that reason but I still very much think the things i mentioned should still be available. I could also see fake sa owners trying to take advantage of this.

The vest doesn't make the dog, the training does. I used a cheap vest from Amazon during a lot of Ollie’s training. It's totally okay to use them! The problem is that people think that getting their pet dog (who doesn't have any training) a harness and “certificate” (they are fake and illegal) means their dog is a service dog and they think that they can take their pet everywhere. I hope that makes sense.

Yeah, it's a huge problem, unfortunately. That behavior is unacceptable, even *if* it was a legitimate service dog (and if it was, that handler needed to leave and get their dog out of that environment and regain control. We all have our bad days and mistakes, but that was just not okay imo). People and their fake “service dogs” make the real Service Dog teams look bad and that's why we have such a bad rep (along with so many other huge issues like safety, access issues, Karens, etc.)

Hi! So, u have a full video about how I set up my feeds if you want to know more about that. Yes, G-J (gastro-jejunal) tubes leak the same as G (gastro) tubes. J tubes are just like g tubes but they have an extension into the small bowel (or jejunum). Granulation is kind of like scar tissue but it keeps getting irritated and the stomach acid leaking sends it in a vicious cycle. It’s super painful because it’s new tissue and it has a lot of nerve endings. When mine is bad, I clean my stoma like 6x a day (depending on how leaky my tube is). Tube pads can help, but when my tube is really leaky, I use gauze because it’s disposable. Plus some tube pads have stitching on the inside, and I got really bad granulation tissue from the friction. That’s why I will use gauze sometimes. I hope that helps!🤍

I have all of that too! I also have dysautiomia, and a few other things, and I really appreciate everyone coming together to support one another!

@starlight_gaxcha7516 💚💚💚

It depends on the person, their symptoms, what medications/treatments they are on to mitigate their symptoms, etc. Not everyone with POTS passes out. It's a choice they should make with their doctor’s recommendation. It's just like any other health issue. Personally, I do not drive, but that's for many reasons and POTS is only one of them. I'm grateful to have someone to help me and drive me where I need to go. But just because I don't drive doesn't mean everyone with POTS can't.

This is totally the behavior of someone who “doesn't care” 💀

Hi! So, I used my sweat and swabs and froze them until I was ready to train. There are some great TH-cam videos that go into depth about it. I have also now trained him to alert hypoglycemia using my saliva. It sounds gross, but that’s the best way I’ve found, or at least that’s what works best for Ollie and I. Thankfully, Ollie naturally picks up a lot of it so scent training was a bit easier once he knew how to alert (using paw or nose, and occasionally “jump” while we’re at home and I’m not paying attention to his alerts). Sorry I can’t give a detailed answer, but there are many videos that can explain it far better than I can. I hope that’s somewhat helpful 💚

@Chronically.sarahdayton thank you so much i appreciate it!!

Thank you! I have a video on my channel of Ollie’s gear tour. That video has chapters and links in the description to everything to make it easier for y’all. That video is linked in the description of this video too. I’ll link it here, but TH-cam has taken the link function sometimes. I hope that helps! Link- th-cam.com/video/NeIBGKlK1PM/w-d-xo.htmlsi=_lGmo7pgWZP_a5VC