she sounds like my wife. these broads are tough as nails. they sent my wife home with a 10 day supply of oxy that last surgery and the night I got her home she was already off it and back to the ibuprofen for a couple days. their pain tolerance inspires me to hide how much I'm in pain half the time lol.Thanks guys….she is doing much better today. Even tried to talk me into hopping in the hospital bed with her. I told that was the Morphine talking, and she said “no they quit giving me Morphine yesterday.![]()
He is going to keep her probably 3 more days and continue with the IV antibiotics and test again Friday to see if she can come home. We like it that they started giving her probiotics and all the yogurt she wants. She wanted me to thank you guys for all the kind words, and the thoughts and prayers you sent her way. She said she could feel the love.![]()
Yeah we were surprised he wanted to keep her a few days extra, but he said because her immune system is probably weak from her MS medicine he is wanting to be safe and make sure.Hey that 230 by 10 is pretty great! aren't we pretty close to PR territory there? I can't remember where you had maxed your 10 rep sets at...
She sounds pretty great, I'm sorry that she has had to stay in the hospital.. thats a longer stay than I would have expected!
He said this one hits some people’s immune system harder than others and after the last couple of kidney infections he said we may need to change.
hmm thats interesting. my buddy has had that issue for years with various a.d.d. meds. he finally came out with a combination/dosage that seems to be dialed in his brain at times would be just a mess. it got to where we could always tell when he changed rx and I'd be like... yo Ian, you left your right shoe and and jacket in the bathroom again, did you change your meds?Honestly those medicines all seem to work great in the beginning for MS, but after a while it’s like the disease adapts and it’s less effective,
You have no idea how much that last comment fits me. LMAO! Thank goodness, I have a high IQ or I would be pretty useless. LOLI was going to ask if that might be playing a role. She goes home this weekend?
hmm thats interesting. my buddy has had that issue for years with various a.d.d. meds. he finally came out with a combination/dosage that seems to be dialed in his brain at times would be just a mess. it got to where we could always tell when he changed rx and I'd be like... yo Ian, you left your right shoe and and jacket in the bathroom again, did you change your meds?
haha yeah I get that. most of the a.d.h.d. people I know are also by far the most intelligent people I know. I can't tell you how many times Ian has left his gymbag in my car when we run down for a lunch session. Or the time we get into my car, drive a 1/2 mile down the road and he goes "oh we need to go back, my gym bag is in my truck"@gphagan1 Man, I know how that can be with the MS stuff, my MIL just finished her chemo / radiation for metastasized lung cancer, and the stress from it has her MS in full effect right now. Poor thing is slurring her words, having a hard time doing any normal physical activities, forgetting what she was saying. Just on the MS Struggle Bus... Her mind takes a MASSIVE HIT when she gets sick, and the MS kicks in. Like it truly just takes her out so hard. She is supposed to come out in 2 weeks but I am not sure if that is ideal or if we should ask her to give it another month so she can recover a bit more, and really enjoy her stay. She will be with us for 3-4 weeks this time, which will be nice to have her around, and after the cancer got so bad they originally just kind of gave her a death sentence we do not want to lose any time with her. Luckily a change in doctors and facilities they came up with a new experimental way to attack it and she got to ring the bell about a month ago!!! The radiation sickness has hold of her now so her MS resilience is crumbling under that load. So this is one MS outbreak I am sure she does not regret.
You have no idea how much that last comment fits me. LMAO! Thank goodness, I have a high IQ or I would be pretty useless. LOL
We’re hoping she can go home this weekend. The MS flare up has her Neurologist just wanting to be very cautious because of how serious this infection was, so the Urologist and the Infectious Disease Doctor, they called in because of MRSA, with her Neurologist will all decide together when she can go. Her Neurologist talked to us this morning and said they don’t want to put a time table on when she can go home because any relapse from the MRSA coming back would be way more serious.I was going to ask if that might be playing a role. She goes home this weekend?
hmm thats interesting. my buddy has had that issue for years with various a.d.d. meds. he finally came out with a combination/dosage that seems to be dialed in his brain at times would be just a mess. it got to where we could always tell when he changed rx and I'd be like... yo Ian, you left your right shoe and and jacket in the bathroom again, did you change your meds?
Man that is very sad for your mother in law…just one of those diseases whether MS or Cancer is brutal, but both of them together I know is a true nightmare. Hopefully the chemo has really helped and her MS will calm down so she can have some relief.@gphagan1 Man, I know how that can be with the MS stuff, my MIL just finished her chemo / radiation for metastasized lung cancer, and the stress from it has her MS in full effect right now. Poor thing is slurring her words, having a hard time doing any normal physical activities, forgetting what she was saying. Just on the MS Struggle Bus... Her mind takes a MASSIVE HIT when she gets sick, and the MS kicks in. Like it truly just takes her out so hard. She is supposed to come out in 2 weeks but I am not sure if that is ideal or if we should ask her to give it another month so she can recover a bit more, and really enjoy her stay. She will be with us for 3-4 weeks this time, which will be nice to have her around, and after the cancer got so bad they originally just kind of gave her a death sentence we do not want to lose any time with her. Luckily a change in doctors and facilities they came up with a new experimental way to attack it and she got to ring the bell about a month ago!!! The radiation sickness has hold of her now so her MS resilience is crumbling under that load. So this is one MS outbreak I am sure she does not regret.
You have no idea how much that last comment fits me. LMAO! Thank goodness, I have a high IQ or I would be pretty useless. LOL
I'm with you there!!!! I can't tell you how grateful I was to be in America with my wife's cancer!!!You know I know I complain about the health care system a lot, but all these doctors and nurses are doing a fantastic job, and I’ve got to say it’s refreshing seeing how much they truly care.
Yeah MRSA is super serious, I don't think many people realize how bad it truly is. While unpleasant to have to stay she should definitely be there until the doctors are comfortable letting her leave. Especially with her having an MS flare up.We’re hoping she can go home this weekend. The MS flare up has her Neurologist just wanting to be very cautious because of how serious this infection was, so the Urologist and the Infectious Disease Doctor, they called in because of MRSA, with her Neurologist will all decide together when she can go. Her Neurologist talked to us this morning and said they don’t want to put a time table on when she can go home because any relapse from the MRSA coming back would be way more serious.
You know I know I complain about the health care system a lot, but all these doctors and nurses are doing a fantastic job, and I’ve got to say it’s refreshing seeing how much they truly care.
Man that is very sad for your mother in law…just one of those diseases whether MS or Cancer is brutal, but both of them together I know is a true nightmare. Hopefully the chemo has really helped and her MS will calm down so she can have some relief.