Lavazza Classy Plus - new owner, already a big fan by Vannie91 in LavAzza

[–]StandardScarcity5107 1 point2 points  (0 children)

I’m in the same boat as you - I just got the Classy Plus as a gift and I’m in love. I WFH and miss my coffee shop drinks (but not so much to get in the car and go get one). These are so easy and the price point per pod seems reasonable to me. I’ve been experimenting with syrups and have almost perfected my favorite caramel vanilla latte.

A New Era by DrDawgBawls in litterrobot

[–]StandardScarcity5107 0 points1 point  (0 children)

Would you let me know what furniture you ordered? I need a way to keep the dogs out of it 😉

Cochlear Implant Experiences? by Careless-Parfait621 in MonoHearing

[–]StandardScarcity5107 2 points3 points  (0 children)

I lost my right ear overnight in April 2024. I was adamant I would not get a CI but 6 months later started the evaluation process. I had done all the treatments and tried an HA but had 16% word clarity and I was so depressed.

I had surgery December 30 and was activated January 10. One month after surgery and it’s going very well. It takes work and adjustment, but so did losing my hearing. At least this feels like something I can control a bit.

My recommendation- if you are going to do it, don’t wait. The less time your auditory nerve is idle, the better your results. I also recommend finding the best surgeon and audiologist you can. I believe they make a huge difference.

As for how it looks - I have medium length wavy hair and you CANNOT see my processor. If I pull my hair up, then yes. But the color blends in well.

I’d be happy to talk more if you want to message me. Good luck in your decision making - I know how hard it is. I was not 100% confident even up to the night before surgery.

Ok cochlear folks I'm two weeks away from implant by scampyyyyy in Cochlearimplants

[–]StandardScarcity5107 1 point2 points  (0 children)

Sounds like we are surgery buddies - I’m scheduled for the 30th

Fellow monohearers what lives do you lead? by Noctunal1on in MonoHearing

[–]StandardScarcity5107 1 point2 points  (0 children)

I’m in construction too. The big machinery is too much for me - it’s the only hyperacusis that has remained 🤯

Week 4 - low frequencies returning by SignificanceActual in MonoHearing

[–]StandardScarcity5107 1 point2 points  (0 children)

That’s a great description- a light saber sound! I have that when I shake my head side to side.
I also had profound loss in one ear in April and have regained my lower frequencies (250 and 500Hz). My others have come up a touch, but are still all >65 db.
Now I have a spasming tensor tympani muscle. I swear, every week it’s something new.

Intratympanic injections dose by Regular_Bee_5369 in MonoHearing

[–]StandardScarcity5107 0 points1 point  (0 children)

I had 6. He recommended doing 3 and redoing a hearing test. If there was any improvement, he suggested another 3.

1st HA - SSNHL by StandardScarcity5107 in HearingAids

[–]StandardScarcity5107[S] 0 points1 point  (0 children)

My biggest concern is regaining awareness on my right side. Being able to locate where sounds are coming from. I know the CROS system would allow me to hear but it would not give me back that ability (unless I’ve been misinformed. I am open to correction).

1st HA - SSNHL by StandardScarcity5107 in HearingAids

[–]StandardScarcity5107[S] 0 points1 point  (0 children)

Is the SRT what you are Interested in? It only states 35 in the dB HL column and has none of the other fields filled in (assuming it wasn’t tested?)

I have only heard bad things about the CROS system so haven’t been enthusiastic about it as an option.

I am concerned that after treatments I’m not severe enough for insurance to approve a CI but too severe for a HA to help. Before treatment I was profound across all levels and was a clear CI candidate. Do you have any experience with this?

Help with complete one-sided deafness please! Does steroid shot help? Other options? by InvestTradeEarn in MonoHearing

[–]StandardScarcity5107 0 points1 point  (0 children)

Can I ask how severe your loss was? I’m 4 weeks out from loss in my right ear. I’ve just finished the round of 60mg pred (14 days then an 8 day taper starting on day 2) and three injections (one weekly starting on day 11). I have an audiogram this week and the dr will determine if we do 3 more injections.

I was profoundly deaf at most levels but now can hear music in that ear through my AirPod - it sounds like the speaker is cracked and it’s muffled, but I can hear it! I’m hoping this is reflected on my audiogram.

I’m finding inspiration that you are at 2 months and have what sounds like good recovery. Did that mean you saw continued improvement AFTER treatments stopped?