Experiences with

Non-Invasive Ventilation

Frequent exacerbations requiring 4 or more courses of prednisolone per year, usually 40 mg per day for 5 days or more COPD on long term home -invasive ventilation (NIV). Patients on long term oxygen therapy.

Hello, I'm Josaphat from Madagascar. My first symptom for Behçet disease appeared in Mars 2020. I had sores in my mouth. After that It started to appear my genital. I consulted doctor for many times and they always suggested me to use either antibiotics or aciclovir. With time, my situation became worse

Back again with an old problem. Had my cryoablation 15 months ago and went through the usual recovery with the help of all you nice folks. So I need some more help. The past 3 weeks my flutters have been returning. I've been stressed lately and I'm sure that helped to start them. So I went on Klor-con

“If a patient’s blood oxygenation level continues to deteriorate despite non-invasive efforts, such as an oxygen mask, then invasive mechanical ventilation becomes the only option of treatment,” explains Prof.

Hello this is my first time posting so be kind. I have MS and have been prescribed Klor-Con M20 potassium as a result of diarrhea. Now I am having Trigeminal Neuralgia (TN) events sometimes 3-times per day and as you know if you have had them they hurt. I read somewhere that a person said to avoid bananas

I was given small amounts of Oramorph for my breathlessness which seemed to help as well as my nebulisers and my non invasive ventilation machine. since being released from hospital I have have noticed there are times in the day when I am at home when I start to slowly panic and have to try and calm

Somebody on FB had a link to a Noni Juice Cures PD page (they were selling Noni Juice) so I figured I would look for some science behind it. I will probably add this to my diet. Morinda citrifolia mitigates rotenone-induced striatal neuronal loss in male Sprague-Dawley rats by preventing mitochondrial

or invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO) with a recommended dose of 4-mg once daily for 14 days or until hospital discharge, whichever comes first.

Hello everyone, My dad has been on a ventilator due to covid for nearly 7 weeks now, the last week they have been weaning him off the ventilator and sedation, he has done so well with his breathing they have put him on a high flow oxygen (via his trachy) so a form of non invasive ventilation and been

I’m extremely vulnerable being on oxygen and non invasive ventilation but sod that when my husband needs help. He went to hospital checked and sent home with antibiotics where later on he promptly collapsed again.

So I went to get blood work done today because I started 25mg Synthroid (brand name) two weeks ago but because I have been experiencing runs of NSVT (not SVT) and slower than normal heart rate (in the 50s) they wanted to repeat it. They also had me stop the Synthroid yesterday until we figure it out

We found that patients with prior use of ⍺ 1- AR antagonists had 12.9% lower incidence of mechanical ventilation compared to non-users (OR = 0.86, 95% CI 0.78-0.95, p = 0.002; AOR = 0.83, 95% CI 0.75-0.92, p < 0.001).

It’s open to those who have non invasive ventilation (NIV) or someone who cares for someone who had NIV treatment. Here’s the link https://www.facebook.com/groups/79190966928/?ref=share I have been given permission from BLF to post this. Thank you

I have severe RLS. It has mostly been under control for awhile after years of different meds. All of a sudden, for about 2 months now it’s like I don’t even take any medicine. It’s been a nightmare. And I haven’t been able to understand why? Last night out of desperation I was looking at all my meds,

Well he became very ill on Feb 1 and was blue lighted to hospital, put on iv antibiotics, steroids etc. and in the end was given non-invasive ventilation. I was told to prepare for the worst but he battled through. Then his heart rate went through the roof (220bpm).

I have severe COPD and have had it for about 10 years, my consultant at the hospital has loaned me a NIV machine ( non invasive ventilation machine) because I am a CO2 retainer which I use during the night.

invasive ventilation and hard lungs still not absorbing oxygen very well at the moment I use it 10hours every night and 4 hours during the day I have to carry special warning cards about asthma attacks whilst having this condition as you can’t be ventilated mechanically I have to go back in 3 months

Hi my MPN friend, lot happening from my last 3-4 month. I have Et for 26 years only on aspirin and platets was 400-500, but after holidej (long flight) my hct go up to 48 and put me on venosection for8 month , was bad and put me on interferon weakly (only 5 weaks) and my old hemo. Told me I have PV

I have severe breathing problems and on non invasive ventilation. I just wanna know I don't feel too good. My chest feels heavy and painful but can you have a chest infection without a cold & cough? & when I take my ventilator mask off my SATs drop & i am breathless.

Here is a list of the medications that can impact swallowing and why this happens: Dysphagia as a side effect of medication Medications that affect the smooth and striated muscles of the esophagus which are involved in swallowing may cause dysphagia. Medications with anticholinergic or antimuscarinic