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.

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

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

This paper should be of interest to any patient who had RT after his prostatectomy or is considering it now. It was of special interest to me, as I pushed for and got adjuvant IMRT at just 3 months after my RALP surgery. [i](Rather that the 6-month wait-period that was common at that time.) [/i]My push

I have completed one session of brachytherapy in Sept and am currently undergoing 25 sessions of whole-pelvis IMRT administered by MSK (details in my bio). Despite a low Decipher score, my cancer has adverse features, including cribriform and gross EPE. I am considering extending Orgovyx to a total of

so I had an mri in area of pain ( lower back) and no Pca found. So given I have only 3 bone mets per CTPETPSMA , my next step should be imrt to those Mets, correct?

I underwent 35 sessions (70 Gy) of IMRT salvage radiation therapy (SRT) to my prostate bed only in July and August 2022. Now, 27 months after the radiation ended, I am seeing traces of blood in my stools about 10% of the time. There were a couple of instances where the spots were more noticeable. The

Please see my bio for my situation. One arm of the Stampede trial compared ADT alone to ADT+Abiraterone for high risk PCa. This resulted in a "Strong" recommendation in the European Prostate Cancer guidleines: [i]"Offer IMRT/VMAT plus IGRT to the prostate in combination with long-term ADT and

Basically the title. Now that my cT3b is, after PSMA PET scan revealed a sub-cm (7mm) pelvic lymph node lesion, cT3bN1, my agreed-upon RT plan (28 IMRT fractions to the whole pelvis, followed by 5 fraction SBRT boost to my prostate tumor) is in question. My insurance won’t likely approve any SBRT or

Full details in bio. PSA trends and question below: 09/2021, before RP: 45 10/2021, after RP: 4. 12/21, after one month of ADT + abi: 0.04 01/22, just before IMRT began: 0.01. 04/22, after IMRT completion: <0.01. 04/202 — 02/2024: uninterrupted, no variation, same lab, same equipment, monthly tests

At the 1st visit with the MO consultant, bicalutamide and Leuprolide injection was recommended for 6 months before 20 IMRT sessions and HDBT plus continuation ADT for 18- 24 months. There was also mention of chemo, but I've explained I would like to leave that for later, if required. Clinical trial of

Hey Warriors Just a quick update note. Feel free to comment if desired, however no responses are required or expected. It has been a year since diagnosis via Biopsy. GG3 (Gleason 4 +3) cT3aN1M1a. PET Scan showed in addition to PSMA uptake on Prostate gland, PSMA uptake on Pelvis/Iliac Lymph Nodes

Hello all, my husband is 10 months out from his IMRT radiation and for the past week every now and then he gets a little burning sensation at the start of the urination. It’s every now and then but not every day. He’s on monthly Firmagon injections. He had a blood test on Thursday when he got his injection

Hi all. First post in this group (I am also on APC). I had a busy week meeting with MedOncs and RadOnc as I’m about ready to start treatment. —my very high risk cT3b is now regional N1 with a 7mm pelvic sidewall node lesion (SUV 3.5) Because I’m not on Medicare, “it’s a coin flip” per my RO whether

Hi all. Update after a busy week meeting with MedOncs and RadOnc: —my very high risk PCa is now regional n1 with a 7mm pelvic sidewall node lesion (SUV 3.5) Because I’m not on Medicare, “it’s a coin flip” per my RO whether my insurance will cover the planned SBRT boost, since it’s not NCCN standard