Experiences with

Ovestin

I prefer t[u]o not[/u] use something like Ovestin. Does anyone have any info on the Best Bio-Identical Oestrogen Cream. If from personal experience that would be great.

Do you think ovestin could trigger an endo flare? Could it be my own estrogen just happened to sky rocket at the same time I was using the cream causing too much estrogen? The flare seems to be calming down now, but for 6 days I've had this flare and started ovestin 7 days ago, coincidence?

I used Ovestin cream for almost month every night... but i didn feel any change..i am still very dry,painful and intercourse is impossible mision..any advise?

Do you think ovestin could trigger an endo flare? Could it be my own estrogen just happened to sky rocket at the same time I was using the cream causing too much estrogen? The flare seems to be calming down now, but for 6 days I've had this flare and started ovestin 7 days ago, coincidence?

I have stuffed with this condition for yrs after the menopause.I eventually found a good bladder consultant who started me on Hiprex and Ovestin cream . My flare ups are less frequent but still every few months causing great distress .

Hi,I have been using Ovestin 1mg for 18 months. I am 64 and went through the menopause 10 years ago. My GP is quite happy to keep issuing repeat prescriptions but I am wondering if it is safe to keep using indefinitely.

I have had multiple recurring meningiomas with subsequent infections since 2020. I have undergone radiation treatments x2. The first was 5 times/week x 6 weeks. The next was called TrueBeam. It was only one treatment in November of 2023, but it left me with brain lesions (areas of necrosis on the brain

Hi Ladies I am currently being treated for first recurrence and are getting Carbo/Doxil and Keytruda. I recently had an echocardiogram and it showed a lot of pericardial effusion. I was immediately rushed to ER and then off to radiology intervention to insert a drain. I was admitted to critical care

Lytenava (bevacizumab gamma), is the first licensed version of Avastin for wet age-related macular degeneration. The treatment was approved by the National Institute for Health and Care Excellence (NICE) for use in the NHS last year. Join our monthly webinar as professor Andrew Lotery will break down

Anyone had same situation.? If so...Any vision improvement after shots?

Had AMD for 3 + years and have Avastin eye injections in 1 eye every 4-6 weeks. Overall I have made improvement with little side effects. As of today I have gone to a lower 2.5 strength readers from 3.5 strength after getting 20/20 on eye chart exam. Anyone else have a similar experience?

Had an retinal and arterial vein occlusion which resulted in distorted vision in one eye being a cobweb like result. Was given eye injection of avastin but didnt improve vision. Anyone else have same issue and if so what course of treatment did you do and was it successful in improving vision?

Dear lovely ladies, My mum finished her first line chemotherapy treatment (she has 3a2 hgsoc; hrd negative); avastin was stopped after the first cycle because she had a bacterial infection that caused stomach bleeding (and avastin was never reintroduced after that). Other than this experience, the chemo

My AMD was treated first with Avastin injections but had a rare reaction and was changed to Eylea HD. Now I have a rash that has spread with severe itch. Dermatologist has ruled out every known skin condition and biopsies are negative for cancer. I have read from reliable sites that this can be a reaction

My story is I’m back on tread mill again. Started Chemotherapy again after Avastin didn’t work as maintenance. Disappointing especially as Olaparib also didn’t work for me in 2023. After being mostly bald for the past two years (was told Caelyx wouldn’t lose my hair!). As I now have grown hair

Hello, I’m new to the community. My wife was diagnosed March 23 with stage 4b OC. surgery right away six rounds of chemo and just about to complete her 24 cycles of Avastin. We are scared of death of the lack of a parachute. I’m sure this is a common concern. Not just a physical, but this mental aspect

Hi everyone, I’m on weekly taxol and two weekly avastin. I was told I will be on this now until I can no longer tolerate it or until it stops working. I had a CT before Christmas and had a partial response. My CA125 has decreased from 1250 to 95. My consultant is now saying a partial response is the

So background I have had issues since December 2019 when I first developed CNV and I was given Avastin to help. I received an indifferential dx of PIC/POHS at this time. I received routine injections in my right eye once there was recurrence after the first injection until I became pregnant in spring

hi all. , I was first diagnosed in 2020 and have managed to get here with various chemotherapy’s . Unfortunately , Avastin and Olaparib didn’t work for me. As a last resort I am on Caelyx but after only 2 treatments I am breathless. I had great hopes to move on to Elahere but unfortunately it is not

Firstly, "Merry Christmas" 🥰. My storyso far: I was diagnosed after a blood test in April 22 for minimal symptoms just needing to wee alot! With a CA 125 of 2248 🤯 and after further biopsies,scans and more biopsies Staged at 4b hgsc. My life as I knew it fell apart and would never ever be the same