Experiences with

Atimos Modulite

My doctor changed my inhaler from Atimos modulite to Serevent. I've been using it for two days. My question is how long do you have to use serevent for it to take full effect? Have any of you had experience with this inhaler? Thank you for all your replies.

There I received a prescription for Atimos modulite 12, Flixotide 250. In case of infection, additional Pulmicort and Salbutamol to the nebuliser. I checked all these new drugs to see if they were on the NHS list. It turned out that they are.

Does anyone else experience problems with the quality of their inhalers?. I have been on Clenil Modulite for two years now and over that time I have experienced problems relating to the inhalers. The past two Clenil inhalers I have had have both clogged up and I haven't been able to get any medication

Hello everyone, just want to ask anyone out there experiences with trelegy. I need to stop my duaklir genuair and clenil modulite and try something else as I absolutely can't do anything at the moment because of my breathing. Still really breathless after 2 weeks of finishing my clarithromycin and

I have just been prescribed Qvar 100 after I had to stop taking Seretide 125 due to side effects. I was prescribed the Seretide a week ago as the Clenil inhaler wasn't doing much to control my asthma (waking up several times a night, needing my ventolin inhaler multiple times a day etc). The Seretide

After reading this forum I do feel for the people suffering with different forms of Asthma/COPD. I decided to write this thinking that when I was told I had COPD, to me it was a massive shock, and did not know what to expect, hopefully some of you might see in my post something helpful I am almost

Hi thank you for allowing me to join the group and was wondering if this is still active but I’ll post my query here. white female, 39 years old (38 at time of spirometer) 166cm tall, weight 55.0kg November 2023 I come down with that horrid virus that’s fleeted us and was generally unwell with it,

I have recently seen a couple of posts about taking/not taking Bisoprolol if you have asthma, but does that relate to those inhalers containing Salbutamol sulfate I have been taking 5mg of Bisoprolol twice a day for the past 12 years. (Paroxysmal Afb) plus the same of Ramipril and Doxazosin. Some

My 2nd bcr was 2019. Treatment included imrt 25x to the pelvic floor, abiraterone and lupron injection monthly. Undetectable psa until yesterday. I know at 0.05 the level is very low. It does appear to be my 3rd bcr. What are the next in Treatment protocols? Thank you. I'm receiving care at MSK in nyc

I had physician appointment today for possible hyperbaric oxygen therapy (HBOT) 40 treatments. I had salvage IMRT to bed and pelvic lymph nodes 8/2022. I felt great for nearly 2 years until cystoscopy on 7/31/24 recommended by MO because of a few very very small clots noted in urine but no real blood

I devloped radiaton cystitis 5 years following IMRT & HDR, with blood in my urine and several blockages due to clotting. I was able to find a wound care clinic with Hyperbaric Oxygen treatment (HBOT) available nearby and was able to start HBOT approximately 6 weeks after onset of bleeding. After 10

I’m wondering if others are having the same difficulty that I am. I had IMRT and HDR Brachytherapy 4 years ago along with 12 months ADT. About a year and a half ago I started testosterone replacement therapy since it wasn’t coming back on its own. PSA is remaining undetectable so all is good there. Erections

I just finished Day 11 of 40 days of IMRT. I meet with MO on Thursday. I've been on Lupron only since 2018 and I know we'll discuss the topic of adding Zytiga, Xtandi, Darolutamide, of Erleada. Is it OK to add any of those while I'm early into radiation?

Update from Doug Adv Pca St IV. Taking Abiraterone 250 mg and Pred 5mg daily since 2019. PSA still 0.2 to 0.3mg/ml last 3yrs.. Radiated my prostate IMRT 42x’s Sep-Dec 2005. Last 6 months 19yrs later I’m having Urethral issues. 1. I self Cath 7-8 X/day. Urinary retention since July 2005 2. neurogenic

On sept 2023, radical prostatectomy with Gleason of 9, multifocal Extra prostatic extension, with negative margins , negative nodes and negative seminal vesicles, PSMA negative. At month 6 PSA started to climb, reaching 0.2 at month 8(May) post RP. With a negative MRI and PSMA, I started Lupron injection

Was diagnosed in 2023 with PSA of 8.9, after a biopsy was found to have 2 lesions 1 was benign and 1 was a Gleason 6. Fast forward a year and my PSA went up to a 13.9. Had a second biopsy and was found to now have 3 lesions, 1 benign, 1 a Gleason 6 and a third that is a Gleason 7 (3+3=6, 3+4=7 unfavorable

I had blood work this past week and the Pathologist did a perioperative (for knee replacement) analysis for anemia. They determined that I have mild ACD, Anemia of Chronic Disease. It is usually caused by inflammatory disease like cancer. The symptoms are the same as the ADT drugs except for the loss

I'm on Orgovyx + Abi for three months, (started recently) hoping to shrink my prostate to assist IMRT. After IMRT I'll have brachytherapy . I'll be on Org/Abi for 12 or 18 months, depending upon the outcome of that test that assesses aggressiveness. My cancer is Gleason 4+4, a small extension (~5mm

Currently one month into a 24-month sentence of ADT (Orgovyx + Nubeqa) for my node-positive PCa. IMRT starts early January. My side effects are milder than expected, mainly hot flashes in the evening and overnight. However I am quickly growing tired of waking several times a night as these hot flashes

Has anyone heard of any preliminary results of the PACE-C trial? I am looking for any clinical data regarding the long term effects of SBRT on patients with advanced prostate cancer, if anyone knows of any other studies please share. We are deciding on salvage treatments after RP. IMRT is the gold standards