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.

my pharmacy have told me they won’t be ordering any more of my Clenil Modulite 200 as it’s been discontinued. I’m really panicking as I’ve been on this medication for 25 years and my asthma is well controlled and the thought of changing meds after 25 years is making me feel like I’m going to have an

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've been on Orgovyx + Abi + 5mg Prednisone now for 3 months. I've had to hound my doc for an A1C and lipid profile, since these are known to affect them. My A1c has moved from the upper range of normal to well within diabetes. It was 5.5 and is now 6.7, ouch. That 5mg of prenisone is like eating

Hey Guys, I would like to glean some collective wisdom/experience from this amazing group. The end of this month will mark my one year anniversary of Salvage radiation therapy IMRT / IGRT Conventional Fractionation 7000 cGy / 35 fractions to prostate fossa concurrent with 5000 cGy / 25 fractions

Post my dad’s PC diagnosis in Dec 2024(PSA:38) with semi vesicle invasions, we started firmagon injection. After 3 month firmagon, dad’s MRI review shows left semi vesicle involvement,PSA dropped from 38 to 1.4. Doc suggests prostatectomy. Post second opinion with RO we were advised to undergo VMAT

I started 24 months of Orgovyx and Nubeqa back in October. And I completed 28 fractions of IMRT two weeks ago. I have noticed a not-insignificant case of gynecomastia that has progressed over the past month or two. No tenderness associated with this by the way. After meeting with my MedOnc last week

I'm 78 years old. In May/June 2024 I had 44 sessions of IMRT. I've been on Orgovyx for one year. The ADT is really affecting me - I've gone from a very active happy life to one that is quite dreary. The main SEs are lack of energy and weakness. My urologist and RO want me on Orgovyx for at least

I was told SBRT is not appropriate for high risk GS 9? Could Prostox confirm this over IMRT or CMRT?

Hello Everyone. Been a little while since I've posted but, unfortunately, I am back ; ) I am 57. Had RP in October (2020). Pathology was G9 pT3bN1M0 with ECE, SVI and positive margin. Had 39 IMRT salvage radiation sessions with 18 months of ADT (Lupron and Zytiga). PSA was less than .05 and testosterone

I was diagnosed with oligometastatic PCa in Feb 2022 (see my profile). I had one met in my right iliac crest. I had 37 fractions of IMRT (including to the met) and completed 2 years of ADT which ended in April 2024. My PSA has been undetectable (<0.025 ng/mL) in my three monthly tests since June 2022

Is this standard procedure?

Updated my profile. I have never been undetectable, now 0.58. Two years post surgery and one year since IMRT. Anyone else similar? I have had low grade bladder cancer, removed, and almost finished intervesical therapy. I have appointment with M.O. on Thursday. Any ideas or comments?

Hi all. I’m looking for advice and opinions to help me make a wise decision. 74 year old diagnosed in June 2023. PSA:16.23. MRI: 1) multiple prostatic nodules with prostatic capsule maintained without evidence of metastatic spread. 2) few mildly prominent mesorectal lymph nodes, etiology uncertain.

Good Morning My husband was diagnosed with Gleason 9 in July 2023 with PSMA showing questionable node in pelvis. He had 26 rounds of IMRT whole pelvis radiation in November and December 2023 and has been receiving monthly Firmagon injections. Monthly blood tests have been good with PSA less than .05