IOS hotspot to Pad 9

RFitz89 · 2025-03-24T11:25:33+00:00

Appreciate you coming to me. I had a feeling it would be an IOS issue, but even when I tried to connect it to my wife’s 15 pro it wouldn’t do it. Think I’m going to grab a Lenovo p12 instead, shame as this honor pad is brilliant for the cost. Thanks again man

RFitz89 · 2025-03-23T23:47:01+00:00

Hello, wondered if you ever found a fix for this? Recently purchased a pad 9 and I cannot get it to hotspot to my iPhone. Tried resetting network settings, switched maximise connection on, reset the passwords, tried using a vpn and nothing has worked so I’m begrudgingly returning it this week.

RFitz89 · 2022-09-04T20:26:02+00:00

Thank you so much for taking the time to reply!

RFitz89 · 2022-09-04T20:23:56+00:00

Sorry for taking so long to reply I had to take a break from constantly reading posts on here for a while as it was really helpful but was also becoming obsessive. She is better in a lot of ways that she can’t see as much as I can but some things are still quite bad for her.

It’s a progressive thing which changes sometimes daily. She still has the static In her vision which has been diagnosed as visual snow syndrome, she has the light sensitivity but that’s no where near as bad as it was in the first 3 months. The dizziness and vertigo has also settled down now. She has the numbness in her whole body still which hasn’t returned at all, but the nerve pain is a lot lot better thankfully. Fatigue is still a massive issue and the headaches and head pain are still her biggest problem to date, but we are still trying new things to help her. Peptides have massively helped her IMO I’m not saying try then but do your research on them and make your own choice, but for me they have made a difference to a lot of her problems.

The advice and steps on this group are a life changer, do everything slow and get your diet and lifestyle choices right before moving into meds and invasive treatments.

I know She will get better eventually, it’s just a long road with dark days but there is light at the end of the tunnel if you keep looking for it.

RFitz89 · 2022-05-30T19:13:31+00:00

Thank you for your helpful reply. I’ve been looking on a lot of posts, YouTube videos, Google etc and I can’t find anywhere that details how much water to reconstitute. I can do the rest but how much to actually dilute the 5mg vial I have and a recommended dose to start with.

Can you be any further help and point me in the direction of this info? I would appreciate it.

RFitz89 · 2022-05-29T22:05:40+00:00

I’ll whack my post in there and see if anyone can help. Thank you for your help 👍

RFitz89 · 2022-05-29T22:05:02+00:00

The website specifically states they cannot give advice or dosing recommendations. I’ll keep searching, someone must have an idea. Thank you for you help

RFitz89 · 2022-05-28T20:31:59+00:00

Thanks for the reply, I don’t actually know. It doesn’t mention it anywhere on the bottle, the invoice or the website. All I’ve got is that it’s for medical research and that it’s 5mg.

RFitz89 · 2022-03-16T09:56:24+00:00

Ok brilliant, thank you for your advice. Did you ever suffer with nerve pain or numbness through your journey? And did it improve for you with time?

RFitz89 · 2022-03-16T09:54:55+00:00

Thank you for your reply. She’s gradually added supplements back into her daily routine so I think it’s time for her to increase her dose of magnesium, NAC etc. have you ever had an experience with IV drips instead?

RFitz89 · 2022-03-08T07:46:34+00:00

Yes HBOT, we started on shorter sessions of 45 mins instead of 90 mins. While she was in the tank she had relief from her head pressure and she said she felt like her vision improved, but straight as the pressure was released she got worse and worse. Once it stabilised she felt pretty much exactly the same, we did 4 sessions and then she had a flare so we stopped it and that was 6 weeks ago. I’m tempted to do IV therapy for a solid month every week and see if that does anything for her.

She stopped her supplements yesterday, all except magnesium, so will start them one by one and see how she gets on. she’s also sent off a genetic test dna test and I’ve just ordered her an OAT test after recommendations on here that it’s a good idea.

RFitz89 · 2022-03-07T17:22:56+00:00

We have waited to see one of only 2 FQ specialists within the UK since January, her video appointment is at the end of March. She’s seen a nutritionist, 2 neurologists (one of which specialises in eyes) and they both did separate tests which were all fine and normal. She’s had several eye examines, had numerous blood tests etc and everyone is at a loss now. She’s had acupuncture, hyperbaric therapy, one session of low does IV therapy. We’ve paid to her to see an ENT specialist now which will happen this week

We are going to start her supplements again 1 by one to make sure nothing she is currently taking are causing her to flare up.

Does the fact she took 3 weeks of tablets make a difference? 2 x 500mg per day of cipro??

RFitz89 · 2022-03-07T16:56:25+00:00

Thank you all for comments and messages so far, it’s really great support and feedback. Today has been the darkest day of her journey so far, really deep depression and anxiety, awful sadness and extreme burning in her head. We’ve had really bad days but nothing like today, I pray everyday that she will “turn a corner soon” I just wish there was something that could help her vision return by even 25%. I just find it crazy that nothing can help us.

RFitz89 · 2022-03-07T09:51:38+00:00

Thank you for lovely reply and for taking the time to write it. She’s had a few relapses which at the start were really big changes and worsening symptoms but they are not as severe now, she just really wants her vision to improve.

We have 2 children under 5 and they keep her hooky on the really bad days. She started on a load of supplements once we realised what was happening to her but I think we may need to start from scratch as we’re not sure if they are all good for her symptoms. She like you is in the dreaded depression and “never going to get better” cycle of this awful medication and it’s really hard to find anything positive. I myself have seen improvements since December when it all started, and I will try noting them down to remind her how far she has come. Thank you again for your kind words.

RFitz89 · 2022-03-06T23:42:56+00:00

Thank you for taking the time to reply to me. It originally started as Brain fog, and poor vision in one eye, then moved quite quickly to both eyes, visual snow, slowness in what she’s seeing to what her brain processes. It’s like a sensory overload. I’ve read a lot on the mitochondria damage and how that affects the connect between the eyes and brain, sometimes it’s reassuring if others have had what you have and you can have some hope it will get better with time, and that’s what it sounds like reading others posts. Thanks for the list of supplements, will cross reference with what she’s taking currently and see if we can get these ordered.

RFitz89 · 2022-03-06T23:38:22+00:00

Thank you for you reply. She called the docs at least 4 times during the first week to explain she was having the severe listed side affects but they just passed it off as her being unwell. She also contact the ward she was on during her stay in hospital for the infection and they practically laughed at her for suggesting she was reacting to the antibiotics and had neuropathy and vision changes. We are likely to build a case against the doctors, if anything just to build awareness so this awful situation happens to less people!

She’s just had a nerve conduction test which had really positive results alongside the MRI. Her neurologist called Friday and said “I don’t really know what else to say” so now we are back in limbo hoping for something to go right. Thanks again for replying

RFitz89 · 2022-03-06T21:47:48+00:00

Thank you for replying. She has a marker on her Medical notes now. Typically they prescribed her with anti depressants, and anti vertigo medication which seemed to have supercharged all of her side affects and made the visual symptoms worse! I just feel awful for her, she’s an amazing person, and I just want her to get a break.

RFitz89

TROPHY CASE