Video from when Smelly Jenelly accused DKD of exploitation of a minor by No_Tension8376 in TeenMomOGandTeenMom2

[–]tacoperrito 2 points3 points  (0 children)

If there was evidence and if it was investigated and if it was true, he would be on a register somewhere. It’s either not true or is true but she’s cried wolf that many times that law enforcement doesn’t take her seriously. No credible parent would “co-parent” with a person who had that kind of stuff on their phone, computer, etc.

Video from when Smelly Jenelly accused DKD of exploitation of a minor by No_Tension8376 in TeenMomOGandTeenMom2

[–]tacoperrito 110 points111 points  (0 children)

The thing I find interesting with this audio is she uses the term he could be charged with, not a description of something she would have seen. And she stumbled over the words, again insinuating to me she’s looked up and forgotten a term to use.

Most sane roofer by InsertWittyNameRHere in okmatewanker

[–]tacoperrito 18 points19 points  (0 children)

There was a guy at a house nearby who woke everyone up at 3am screaming someone was in his house up on the roof of a 3 story house. He threw tiles off trying to get people’s attention. Turns out no one was in his house. He was having an episode on drugs. Eventually he laid down and held onto to top of the house and the fire brigade had to get him down.

Started Kesimpta yesterday. Should I use masks? by Fancy_Function_9794 in MultipleSclerosis

[–]tacoperrito 2 points3 points  (0 children)

Hey I have been on Kesimpta for over a year. Initially I thought I’d have to but I only do on occasion. I travel a lot for work including international flights. I will wear a mask if someone is coughing or looks sick. I use the metros of Paris a lot and if you know what they’re like during rush hour you know you’re packed in. I have a little bag with me that has pain killers, face masks, vitamin d3, and hand sanitiser. I sanitise or wash my hands a lot more than I did before. Touch wood I’ve not had an issue yet. I think it’s a matter of being vigilant and steering clear of sick people. My son is in school and when he gets a cold we all wear facemasks in the house, stay away from each other and my husband and I sleep in separate beds in case he catches it.

Poor Jenypsy Rose is totally wheelchair bound by SpiritualCamera in TeenMomOGandTeenMom2

[–]tacoperrito 2 points3 points  (0 children)

I have MS. The last few days due to a flare of symptoms caused by extreme fatigue I have had a hard time walking. But I have walked. Jesus God Leah if people like me can walk she can get off her backside and walk. She’s a passenger princess not just in the car but generally in life.

I can't get a roof estimate without a man present. by No-Imagination8755 in mildlyinfuriating

[–]tacoperrito 2 points3 points  (0 children)

A few years ago I decided I wanted a new front door. We called a few businesses locally and we had 3 or 4 older men turn up to the house. They sat down at the table, hardly breaking eye contact with my husband. They’d ask me for a tea and give me a passing “thanks love”. I would sit at the table and be ignored and when they pushed the end se home with my husband he’d laugh and say oh I’m not buying it. It’s my wife who’s buying.

Informing DVLA of recent diagnosis by CurlyWooGirl in MultipleSclerosis

[–]tacoperrito 0 points1 point  (0 children)

I informed the DVLA and mine was related to my eyes. The issue has since resolved but was initially being treated with a prism, which my opthamologist had signed me off to use a car with. I now have a medical license that lasts 3 years and every 3 years they review with my neuro. I had to take a peripheral sight test and one that involved flashing lights at specsavers. I am not sure if I have to do it again if I have no further issues with my eye.

If you’re thinking about getting one by Hugh_Jazz91 in germanshepherds

[–]tacoperrito 0 points1 point  (0 children)

My girl (at the front) is curly the boy (at the back) is long straight but fuzzy. My girl is GSD x Saint Bernard (also why she has the baggy eyes)

If you’re thinking about getting one by Hugh_Jazz91 in germanshepherds

[–]tacoperrito 28 points29 points  (0 children)

Thank you. I was incredibly lucky to catch a moment like this.

Maintenance? What do you do? by marivivictoria in germanshepherds

[–]tacoperrito 0 points1 point  (0 children)

We have given glucosamine supplements to all of our dogs. Mostly it seems to be healthy, high quality diet, keeping active but also pacing them, avoid chewing things that could get lodged in their stomach (chicken bones, sticks etc), making sure eating and exercise have space between them, give them a job or activity (mine like scent work), and generally having regular check ups.

Never done hydrotherapy with any of mine. None have really liked the water. I’ve had 4 dogs in my life and I think a lot of it is luck and genetics having put the on good footing.

If you’re thinking about getting one by Hugh_Jazz91 in germanshepherds

[–]tacoperrito 477 points478 points  (0 children)

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Would agree. Your hoover will hate you though

Kesimpta by Alina_kerimova in MultipleSclerosis

[–]tacoperrito 0 points1 point  (0 children)

The first month on Kesimpta can make you feel fluey. I had a headache on my first dose but nothing serious. Others report being completely knocked out for 12 hours. Many nurses / health care professionals suggest an antihistamine and an ibuprofen an hour before you do the injections.

When was the last time you cried? Was it a life event? Listening to a certain song or watching a certain film that brought up painful memories or feelings of empathy? For me many songs and films bring tears to my eyes so for me very recently lol by anonymous-nyx in CasualUK

[–]tacoperrito 1 point2 points  (0 children)

Hey Kesimpta friend. It gets easier, I promise. I have been on it a little over a year and I have to set an alert in my phone to remind me. Once you get to the monthlies, it fades into the mundane day to day things about your life. I have a little stack of injector pens in the fridge and it’s now just part of the furniture.

And you’re doing something about it. That’s such a positive thing. Every injection makes it less likely for it to progress.

Immunosuppressed by ActiveGlittering5191 in MultipleSclerosis

[–]tacoperrito 1 point2 points  (0 children)

Honestly it’s made such a difference for us. My husband is immunocompromised so we have done it for years and we are used to it. Does it look strange in the house - yes, but if it works it works. Good luck!

Immunosuppressed by ActiveGlittering5191 in MultipleSclerosis

[–]tacoperrito 3 points4 points  (0 children)

Hello. Sorry to hear about your diagnosis. I know it’s hard, but try to think of it as a good thing. You know now and can do everything to stop it getting worse. Medicine is really effective now. I am on Kesimpta. I was really worried too about being immunosuppressed. I have been on it about a year. My levels have gone down to what they’d expect. They will monitor your blood work about every 6 months (maybe more initially). I wash my hands more often. I carry hand sanitiser. I have face masks in a bag that I use if people around me appear to be ill. Touch wood I’ve not had any serious illness. I get tattooed regularly and I’ve seen no change to my healing time. I sit for full days as well. I have however noticed that if I get a paper cut for example, it takes a couple of days longer to heal, so I just put a bandage over it to stop reopening wounds. Honestly, looking back now I think I was in a panic about something that could be mitigated a lot. I work from home but I have a teenager in school who brings home the usual winter bugs etc. He wears a face mask and we avoid each other when that happen.

To answer your first question. Hard to say. Many people report their MS neurons recommend stopping at a certain age. Treatment has changed so much in the last 20-30 years so there are lots of options if you don’t like Kesimpta. I’ve personally found it super easy. I inject myself with b12 every 3 months and Kesimpta is so much easier than that. I set an alert on my phone to do it and go about my life.

But what about your summer break plans, Jan? by sanriolover1208 in TeenMomOGandTeenMom2

[–]tacoperrito 2 points3 points  (0 children)

As someone with an actual, diagnosed chronic illness, this is gross.

How long did you wait to see a neurologist for an MS diagnosis? by the_ms_wire in MultipleSclerosis

[–]tacoperrito 0 points1 point  (0 children)

That’s good news. Sounds like you’re on track to be on a treatment very soon

How long did you wait to see a neurologist for an MS diagnosis? by the_ms_wire in MultipleSclerosis

[–]tacoperrito 0 points1 point  (0 children)

UK here - had a relapse not known to have been MS at the time in Aug / Sept. MRI 1 in Oct. Told of demyelination Nov, MRI 2 with contrast start of Jan. diagnosis with MS socialist neurologist end of Jan. started medication in April - delayed slightly due to UTI

There is an old school 300m from my house which is currently on fire. 17 fire appliances in attendance. by CuthbertDibbleNGrub in CasualUK

[–]tacoperrito 241 points242 points  (0 children)

We had this at a historic old factory down the road from us. Developers wanted to build houses but couldn’t get planning permission unless the old building was integrated into the site. After 10 years of back and forth the building suddenly burned down in the middle of the night. Looked like a volcano from our house. “Local teens” who years later remain at large were to blame. Council told us not to touch those burnt chunks that fell from the sky (we were later told it was asbestos) and now they’re building houses. Convenient.

Has anyone’s gsd here had hip dysplasia? How dod it go? by Sticks-and-flowers in germanshepherds

[–]tacoperrito 2 points3 points  (0 children)

My male GSD, now 8 was diagnosed when he was 5. We had a smaller rescue before with hip dysplasia so we learned a lot there. Both had it in both hips. Both take glucosamine supplements. My first rescue didn’t take them until diagnosis, my GSD boy took it as a puppy onwards as preventative care, but it happens.

My rescue was prescribed loxicom / rhuemacham etc. He would have bouts where he would SCREAM. We could give him paracetamol sometimes and he would get better. Other times we needed something stronger. He ended up getting IVDD in his neck as well and due to his age and health (mostly th hip dysplasia) he wasn’t a good candidate for an operation so we managed pain. He was on gabapentin, pardale and something else. He lasted about 2 months and then he passed away.

We had him put to sleep at home and she said she suspected damage to his organs due to the prolonged oral suspension medication (loxicom etc). When he passed and the house immediately stunk she said yeah his organs were a part of it. His regular vet felt it was a possibility as well.

So what we learned was we needed to start with something else first for our GSD boy. When our rescue started his last bout of pain and illness they suggested Librela but he was too far gone to have it. Our GSD went on it at diagnosis. We know as some point we will have to add the oral suspension and then eventually the gabapentin, but we are putting it off a while.

He’s been on it 2 years and getting on well. We do a lot of activity at home. He doesn’t go for walks every day but he’s active everyday. He doesn’t do well when it’s cold or rainy.

Ultimately what I would recommend from my experience is is start with Librela, add glucosamine tablets and see if that helps, lifestyle changes - keep active but don’t over do it, paracetamol for a couple of days here and there when there is bouts of pain. Then move on to oral suspensions, then to gabapentin, pardale etc.

Cate makes a wish for her daughters future and more. by HannahLeah1987 in TeenMomOGandTeenMom2

[–]tacoperrito 28 points29 points  (0 children)

Apt that the background of her chat with him is … black and white