Experiences with

Atimos Modulite

Hello, can anyone help please? My doctor has moved me from a symbicort 100/6, one puff twice a day to Clenil Modulite, one puff twice a day. Has anyone has had a similar change and if so, what are the pros and cons please?

I’m newly asthmatic (started treatment end of January - currently on Ventolin and clenil modulite inhalers) I’m relatively well controlled but it is all still very new to me. I’m due to travel on a plane next week for 10 hours and I have no idea how my asthma will be while on the flight. Has anyone got

I have been dignosed with Hyperventilated lungs but have been given no info. I am exhausted most of the time and cannot walk more than 100 metres without having to rest. Can anyone tell me if this is normal. Is there any medication for this condition? I use Clenil Modulite inhaler 200mg. The waiting

Anyone had any problems starting this inhaler?, I find myself quite heavy on the chest and taking sore heads, been on this for 4 days after being switched from clenil modulite, thanks

I have been taking fostair for some months. As I get use up the doses, the inhaler gets clogged up. The cleaning instructions say wipe the mouth piece inside and out, but you don't wash it like you do the clenil modulite inhaler. The hole gets clogged up over time as wiping it does not properly clean

Ive been diagnosed with mild asthma after waking up one morning with a tight chest (im a fit and otherwise healthy non smoking 40 year old). I currently have 2 doses of 100mg Clenil Modulite twice a day and have been doing so for over a year. I also sing in a band and in the last 2-3 months ive noticed

I am taking Clenil modulite 100 two puffs a day. Getting really nasty raised red spots all over my chin and around my mouth. Can anyone help please, would really appreciate your thoughts on this.

Hi all, Just came on here looking for some words of wisdom or advice. It’s really depressing me having my asthma unmanaged when i play football at the moment especially when I’m trying to excel in my football. I’m currently on clenil modulite and have been for around 2 months but really not seeing any

Hi all, Been on clenil for around 2/3months - two puffs twice a day. (I’ve tried to stay consistent but have forgotten a couple of times)However, I don’t believe my asthma is any better when playing football and my airways are still closing up. I’ve tried fostair and didn’t get on with the long acting

Hi everyone I hope you are all well. I have just been given my asthma plan. I have also had my clenil modulite changed to Fostair. Just wanted to ask what your experiences have been with Fostair? Is it a ‘stronger’ inhaler than clenil and any advice of what you have experienced would be much appreciated

Good Morning All , I started my Eligard ( 6 month )on Dec.9 2021, Zytiga ,(250mg ) Prednisone ( 5 mg) on a low fat breakfast on Feb. 1 2022. My Testosterone is at 9ng/dl . My PSA was at 4.19 on Dec. 2021 . My primary dx was gleason 4+3 downgraded to 3+4 by John Hopkins . I had Sbrt , 5 sessions on 2016

I started on 36 months of ADT in Feb 2020 (Neoadjuvant) followed by 44 sessions of IMRT from May 2020 to July 2020 with Continuous ADT from Feb to now. When does the 36 months start from? From the first injection in Feb or from the finish of IMRT in July. I’ve found conflicting answers on line.

I am writing from Spain with universal health care . I received a diagnosis and second opinion from Uiversity of Navara for curative treatment and of course one favored RP . The first opinion IMRT + 18months ADT. I am scheduled for RD (dont know when)but on the report I see possible T3? That to

I asked same question few months ago. I had IMRT in nov 2019 on prostate and pelvis , seminal vesicules: Prostate 60 GY in 20 fractions and pelvis 48 GY boost. Technique IGRT dyamic arctherapy... Starting January 2022, I started having occasional red blood spots on toilet paper. I have no constipation

Hello all. First post. I’m 54, dx with Gleason 9, PSA 45; RP with ePLND September 2021; Stage IVA, pT3bN1cM0; EPE, positive margin, SVI, 8/27 + LNs with LVI, microscopic bladder neck invasion. Persistent PSA six weeks post RP @ 4.0. ADT+abi started November 2021, with rapid PSA response. Has been <0.01

I wrote in a few months ago with a more favorable seeming diagnosis, but little factual information, and left feeling like i had plenty of time to decide on a course of action. After meeting last week with Dr. Johnson at Huntsman Salt Lake (who I really liked, btw), I now need to get on the stick it

Diagnosed August 2019 at 81 yrs with Gl 9 and PSA 6.7. Treatment: Casodex followed by HDR Brachy, 25 sessions IMRT and 18 months ADT. Treatment ended just about a year ago and PSA remains undetectable. Testosterone was 300 just prior to diagnosis but thus far it too remains undetectable. Have always

Hello , Im stage 4 Oligo . Just finished 25 IMRT , 03/08 to pelvic field , taking Eligard , started Zytiga , prednisone 02/01. This is all new for me so I can get worried real quick . Current PSA .04 , down from .22 . Testosterone was <7 on 02/24 and now 03/29 its 9 ng/dl . So is this T reading no good

Good Morning all , I just completed my 25 days of IMRT , Tomotherapy on 03/08/22 to the pelvic region . Also had 3 sessions of SBRT to 1 lymph node in the pelvic area , Oligometatastic 01/13. So I just received lab results yesterday from Univ. of Chicago . AST-(Sgot) 26....... 8-37 ALT-(Sgpt) 24--

Looking for input: Diagnosed in June 2020 with Oligometastatic prostate cancer via CT & Bone scans. (spot on right pelvic bone) / removed prostate via surgery in July 2020, have been on Lupron & Erleada since Aug 2020 & did IMRT radiation to pelvic bone in Feb 2021. My PSA is currently undetectable.