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insurance issue
hi guys, My mother was diagnosed with her2+ve braa we ya cancer stage 4. doctor recommended the below medications : Paclitaxel + cyclophosphamide + phesgo+ zolodronic acid . I have corporate insurance in new India insurance with mediassist. These people are not approving phesgo which is targeted
hi guys, My mother was diagnosed with her2+ve braa we ya cancer stage 4. doctor recommended the below medications : Paclitaxel + cyclophosphamide + phesgo+ zolodronic acid . I have corporate insurance in new India insurance with mediassist. These people are not approving phesgo which is targeted
Srikalakm
in
Breast Cancer India
6 months ago
Proton Therapy Had PT Therapy 15 years (2009) ago 5 year follow Up No Cancer Just Diagnosed with Mets in Bone/Pelvic Lymph Nodes in 2024
Had PT Therapy at MD Anderson 15 years ago with Pencil beam radiation. Gleason at the time 2009 was 6 (3 +3) and PSA was 5.9. I am now 73. Successfully treated and follow up every year for 5 years showed my PSA at between .2-.4. For 15 years up untiil now, no symptoms. According to MD Anderson,
Had PT Therapy at MD Anderson 15 years ago with Pencil beam radiation. Gleason at the time 2009 was 6 (3 +3) and PSA was 5.9. I am now 73. Successfully treated and follow up every year for 5 years showed my PSA at between .2-.4. For 15 years up untiil now, no symptoms. According to MD Anderson,
Rcole727
in
Advanced Prostate Cancer
4 days ago
Treatment stopped
We thought Erlotinib was working for my dad, his tumour had reduced significantly on October scan ( started on drug Aug 23) but Jan scan showed growth, cough back and has been getting steadily worse with weight down to 7 stone ,diarrhoea and debilitating fatigue. Although Oncologist thought a standard
We thought Erlotinib was working for my dad, his tumour had reduced significantly on October scan ( started on drug Aug 23) but Jan scan showed growth, cough back and has been getting steadily worse with weight down to 7 stone ,diarrhoea and debilitating fatigue. Although Oncologist thought a standard
Adaughter
in
The Roy Castle Lung Cancer Foundation
6 months ago
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Excellent speech/voice app for PWP.
FIrst a disclaimer - i am not associated in any way with the app i want to recommend, just a fellow 'parkie' looking for an app to help/complement my speech therapy. I was looking for something comparative with my speech therapy ( long vowels, functional terms, reading, improvized speech analysis..
FIrst a disclaimer - i am not associated in any way with the app i want to recommend, just a fellow 'parkie' looking for an app to help/complement my speech therapy. I was looking for something comparative with my speech therapy ( long vowels, functional terms, reading, improvized speech analysis..
inovator
in
Cure Parkinson's
6 months ago
Low cortisol
My 40 year old daughter has Hashimoto's on T4 /T3 combination therapy for 6 years. Optimal levels plus optimal B12, folate, vit d and ferritin.Dutch test has shown very low cortisol levels throughout the day. She says she doesn't have any stress, doesn't drink alcohol or coffee, goes to the gym 2 or
My 40 year old daughter has Hashimoto's on T4 /T3 combination therapy for 6 years. Optimal levels plus optimal B12, folate, vit d and ferritin.Dutch test has shown very low cortisol levels throughout the day. She says she doesn't have any stress, doesn't drink alcohol or coffee, goes to the gym 2 or
redhead41
in
Thyroid UK
6 months ago
Me again
Hi, here again. He's doing really well. He's out in the chair each day, still hoisted but he was trying to stand and they had to tell him no you're not strong enough yet. Monday he was in the chair when I got there and they didn't put him back to bed until I left. He was getting tired towards the end
Hi, here again. He's doing really well. He's out in the chair each day, still hoisted but he was trying to stand and they had to tell him no you're not strong enough yet. Monday he was in the chair when I got there and they didn't put him back to bed until I left. He was getting tired towards the end
Hidden
in
British Heart Foundation
6 months ago
How Do Those on T3 or Combo Therapy Navigate TSH Obsessed Doctors
After my pitiful NHS results in December ( before starting self sourced T3) my GP increased my Levo to 200mcg a day. I haven't been taking that much, obviously as I'm taking 150mcg of Levo and 12.5mgs of T3. The GP I spoke to said retest February and unfortunately my surgery have been uncharacteristically
After my pitiful NHS results in December ( before starting self sourced T3) my GP increased my Levo to 200mcg a day. I haven't been taking that much, obviously as I'm taking 150mcg of Levo and 12.5mgs of T3. The GP I spoke to said retest February and unfortunately my surgery have been uncharacteristically
Sparklingsunshine
in
Thyroid UK
6 months ago
Oxygen levels
I have had COPD for around 15 years and it is getting steadily worse. I have the normal inhalers , have a air physio device, a nebuliser and recently have been accepted for oxygen therapy. On my last visit to hospital I was given the device that checks your oxygen levels. As I have only had this device
I have had COPD for around 15 years and it is getting steadily worse. I have the normal inhalers , have a air physio device, a nebuliser and recently have been accepted for oxygen therapy. On my last visit to hospital I was given the device that checks your oxygen levels. As I have only had this device
jackwok
in
Lung Conditions Community Forum
6 months ago
Music therapy
https://www.youtube.com/watch?v=yZsQ1FZtHw0 Most of us know about binaural beats, rife frequencies, rhythmic auditory stimulation, multiple wave oscillation etc and may even find them beneficial. I thought this YT video was interesting though, not least because some years ago I experimented with
https://www.youtube.com/watch?v=yZsQ1FZtHw0 Most of us know about binaural beats, rife frequencies, rhythmic auditory stimulation, multiple wave oscillation etc and may even find them beneficial. I thought this YT video was interesting though, not least because some years ago I experimented with
PDKiwi
in
Cure Parkinson's
6 months ago
wax treatments
having had an appointment with the specialist nurse yesterday I have been referred to occupational therapy for some help with my clawed hands. Really hoping I can get some positive help as I do suffer at times with pain and stiffness despite doing exercises. She also mentioned a wax bath treatment which
having had an appointment with the specialist nurse yesterday I have been referred to occupational therapy for some help with my clawed hands. Really hoping I can get some positive help as I do suffer at times with pain and stiffness despite doing exercises. She also mentioned a wax bath treatment which
Clangerscat
in
Scleroderma & Raynaud's UK (SRUK)
6 months ago
stage 3b/c inoperable non small cell lung cancer. Cannot tolerate durvalumab, (pneumonitis) No mutations - any hope?
hi, Im 57 and was diagnosed with inoperable non small cell lung cancer in October 2022. Since then Ive adopted a dairy, gluten & sugar free diet , organic only & prinipally vegan. I take millions of supplements a day plus Chinese traditional Medicine. I’ve had 3 rounds of chemo, then combined radio
hi, Im 57 and was diagnosed with inoperable non small cell lung cancer in October 2022. Since then Ive adopted a dairy, gluten & sugar free diet , organic only & prinipally vegan. I take millions of supplements a day plus Chinese traditional Medicine. I’ve had 3 rounds of chemo, then combined radio
ohayeai
in
The Roy Castle Lung Cancer Foundation
6 months ago
EP consult
The cardiologist I see is not able to provide medical management of my paroxysmal afib due to my low heart rate and low blood pressure (can't risk pushing either value lower), so I am hoping for an ablation. This morning, due to a cancellation, I was able to bring my initial EP consult forward by 1
The cardiologist I see is not able to provide medical management of my paroxysmal afib due to my low heart rate and low blood pressure (can't risk pushing either value lower), so I am hoping for an ablation. This morning, due to a cancellation, I was able to bring my initial EP consult forward by 1
Desertflowerchild
in
Atrial Fibrillation Support
6 months ago
Seyfried press-pulse metabolic strategy for aggressive advanced prostate cancer
I'm writing on behalf of my brother who was diagnosed one year ago with stage four prostate cancer metastasized to the bones. His oncologist initially started him on anti-androgens and radiation with some positive initial results. In the past couple of months his numbers are going in the wrong direction
I'm writing on behalf of my brother who was diagnosed one year ago with stage four prostate cancer metastasized to the bones. His oncologist initially started him on anti-androgens and radiation with some positive initial results. In the past couple of months his numbers are going in the wrong direction
4mybrother
in
Advanced Prostate Cancer
5 days ago
Omg just received the prescription for peppermint capsules 🙈
Hi AGAIN everyone ❤️ This saga is beyond belief🤷♀️ just reading the leaflet accompanying the peppermint oil capsules. First there's a lot of 💩 fillers in it , as well as containing 0.2 ml of actual peppermint oil, it also contains the following. Gelatin, glycerol, purified water, titanium divide
Hi AGAIN everyone ❤️ This saga is beyond belief🤷♀️ just reading the leaflet accompanying the peppermint oil capsules. First there's a lot of 💩 fillers in it , as well as containing 0.2 ml of actual peppermint oil, it also contains the following. Gelatin, glycerol, purified water, titanium divide
birkie
in
Thyroid UK
8 days ago
Update on visit to gp🙈
Hi everyone ❤️ Update on visit to gp yesterday, firstly I will say she was one of the most down to earth gps I've ever seen👍 she had all my information to hand, she'd obviously done her homework which is rare with some , if not all gps today. I took my roseway information and tablets [ NDT] with me
Hi everyone ❤️ Update on visit to gp yesterday, firstly I will say she was one of the most down to earth gps I've ever seen👍 she had all my information to hand, she'd obviously done her homework which is rare with some , if not all gps today. I took my roseway information and tablets [ NDT] with me
birkie
in
Thyroid UK
9 days ago
Covid again - watch this space!- Update
Hi all, remember my post above from last week well I said I would update Monday after the test. You guessed it…. I fell really ill. I went out for a walk Monday morning and wasn’t feeling that bad but Monday afternoon it started taking hold of me, just feeling really poorly (what do I mean by poorly?
Hi all, remember my post above from last week well I said I would update Monday after the test. You guessed it…. I fell really ill. I went out for a walk Monday morning and wasn’t feeling that bad but Monday afternoon it started taking hold of me, just feeling really poorly (what do I mean by poorly?
Investigator1
in
Vasculitis UK
9 days ago
Psa and sacrolotic joint
I was diagnosed with psa 6 months ago .due to scalp psoriasis and swollen toes fingers knee pain ect .does any one else suffer from sacrolitis with there's and there spine neck my hips are so painful should I ask my rheumatology doctor other questions .does this happen with psa .he said my mri showed
I was diagnosed with psa 6 months ago .due to scalp psoriasis and swollen toes fingers knee pain ect .does any one else suffer from sacrolitis with there's and there spine neck my hips are so painful should I ask my rheumatology doctor other questions .does this happen with psa .he said my mri showed
Vic1977
in
Beyond Psoriasis
11 days ago
Things, regimens,etc that are probably RLS worthless.
THINGS THAT DO NOT WORK FOR RLS All of us with RLS/PLMD have slightly different symptoms. We have tried various 'remedies' to try to relieve our RLS symptoms. We have read articles, some interesting, some ridiculous (bar of soap) that make amazing promises. And there is an entire array of things to
THINGS THAT DO NOT WORK FOR RLS All of us with RLS/PLMD have slightly different symptoms. We have tried various 'remedies' to try to relieve our RLS symptoms. We have read articles, some interesting, some ridiculous (bar of soap) that make amazing promises. And there is an entire array of things to
fritz34
in
Restless Legs Syndrome
6 months ago
The Brightwell
I heard about The Brightwell from a friend. It's a centre for neurological and physical recovery and I aim to take my chap for Hyperbaric Oxygen Therapy (HBOT). Has anyone else tried anything like this for anoxic brain injury?
I heard about The Brightwell from a friend. It's a centre for neurological and physical recovery and I aim to take my chap for Hyperbaric Oxygen Therapy (HBOT). Has anyone else tried anything like this for anoxic brain injury?
AngelLeBuff
in
Headway
15 days ago
I turned 47 yesterday, and I've never bothered about aging before but today I feel sad and old and ugly.
I've been in remission from severe MDD for over 3 years. I had minor bouts when younger but I developed peripartum depression with my last child and it lasted 4 1/2 years. I was hospitalized 10 times, tried 16 different medications, ECT, ketamine, TMS. It was a horrific time of my life and I never want
I've been in remission from severe MDD for over 3 years. I had minor bouts when younger but I developed peripartum depression with my last child and it lasted 4 1/2 years. I was hospitalized 10 times, tried 16 different medications, ECT, ketamine, TMS. It was a horrific time of my life and I never want
StillClimbing
in
Major Depressive Disorder (MDD) Support
19 days ago
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