Search
Search
About
Log in
Join
Experiences with
Flomax Relief MR
Posts
Communities
202 public posts
Filter results
Burning sensations
Hi I was diagnosed last month- spent a week in the hospital on IV steroids. Went home ok and today (a month later) my legs are burning hot I can barely walk. Went to the ER and my neurologist said go home he doesn’t want anymore steroids. I am confused and I don’t know what to do for the burning feels
Hi I was diagnosed last month- spent a week in the hospital on IV steroids. Went home ok and today (a month later) my legs are burning hot I can barely walk. Went to the ER and my neurologist said go home he doesn’t want anymore steroids. I am confused and I don’t know what to do for the burning feels
ktaylor8899
in
My MSAA Community
6 years ago
Frequent urination post Brachytherapy
Hi Everyone, The doctor prescribed my husband 0.4 mg (once a day) flomax to take around bedtime to relax the bladder. However, it does not work. My husband has been taking this for about 10 days now and since the Brachy (last Friday) his urination routine has gotten out of control having to go the restroom
Hi Everyone, The doctor prescribed my husband 0.4 mg (once a day) flomax to take around bedtime to relax the bladder. However, it does not work. My husband has been taking this for about 10 days now and since the Brachy (last Friday) his urination routine has gotten out of control having to go the restroom
anthonyq
in
Advanced Prostate Cancer
6 years ago
My introduction
Hello, fellow ms'ers! My name is Shannon, my Dx came in Oct 1999, I was 29 then. I have RRMS. Been on Copaxone, Rebif, then began in the clinical trial for Fingolimod... Began taking Gilenya (aka Fingolimod) as soon as it was approved by FDA for release. Was on it until sometime in April 2018
Hello, fellow ms'ers! My name is Shannon, my Dx came in Oct 1999, I was 29 then. I have RRMS. Been on Copaxone, Rebif, then began in the clinical trial for Fingolimod... Began taking Gilenya (aka Fingolimod) as soon as it was approved by FDA for release. Was on it until sometime in April 2018
Shannondixon
in
My MSAA Community
6 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Results 😪😭
Well im back rough day yesterday. Went to the doctors they said i cant be without meds cause i they said i have aggressive ms needed to be on a medication so they're going to put me on ocrevus while I'm waiting for my insurance to approve it they told me to stay on rebif I am so scared to be on ocrevus
Well im back rough day yesterday. Went to the doctors they said i cant be without meds cause i they said i have aggressive ms needed to be on a medication so they're going to put me on ocrevus while I'm waiting for my insurance to approve it they told me to stay on rebif I am so scared to be on ocrevus
Jackjosh
in
My MSAA Community
6 years ago
Medicine
I have some questions for you guys i was diagnosed with ms may 2011 and i tested positive for the jc virus. I was on rebif rebidose 22mcg but the made me stop it. They said it was messing with my blood work. Im scared to change medication, completely terrified. I dont have many options. Im really scared
I have some questions for you guys i was diagnosed with ms may 2011 and i tested positive for the jc virus. I was on rebif rebidose 22mcg but the made me stop it. They said it was messing with my blood work. Im scared to change medication, completely terrified. I dont have many options. Im really scared
Jackjosh
in
My MSAA Community
6 years ago
Unexplained rash after 2week flolan infusion
I had a 2weeks treatment of flolan infusion which ended on friday. I noticed a small pimple on my left jaw line on thurday and noticed another one on my chick on friday after my last infusion. I felt it might just be stress after the last treatment. But Saturday every thing was ok when I just decided
I had a 2weeks treatment of flolan infusion which ended on friday. I noticed a small pimple on my left jaw line on thurday and noticed another one on my chick on friday after my last infusion. I felt it might just be stress after the last treatment. But Saturday every thing was ok when I just decided
ijeasike
in
LUPUS UK
6 years ago
Here I go... LDR Brachy seed guys say HEY!
Hi all. Been a few months... Having LDR seed procedure at MSK tomorrow with Dr. Zelefsky. I had another MRI which showed the tumor unchanged from the MRI in October, but evidence of prostatitis, which I could have told them! I wonder if this was from the biopsy? Who knows. Bloodwork and chest Xray fine
Hi all. Been a few months... Having LDR seed procedure at MSK tomorrow with Dr. Zelefsky. I had another MRI which showed the tumor unchanged from the MRI in October, but evidence of prostatitis, which I could have told them! I wonder if this was from the biopsy? Who knows. Bloodwork and chest Xray fine
PianoMan212
in
Prostate Cancer And Gay Men
6 years ago
New to all this. Not even sure what to ask.
Hi all, I am 52, just diagnosed in February with AdvancedPC. My PSA shot from 3 to 130 in less than 12 months; Gleason 9. Lymph nodes in pelvic area; negative in bone scan. Started immediately (early March) with Bicalutamide and Lupron shot 2 weeks later. I am taking Bicalutamide and Flomax daily (in
Hi all, I am 52, just diagnosed in February with AdvancedPC. My PSA shot from 3 to 130 in less than 12 months; Gleason 9. Lymph nodes in pelvic area; negative in bone scan. Started immediately (early March) with Bicalutamide and Lupron shot 2 weeks later. I am taking Bicalutamide and Flomax daily (in
chillywilly
in
Advanced Prostate Cancer
6 years ago
Slow recovery from Chemo, Round 4, Session 2
PSA 1124, Age 59, Stage 4, Dx 3-22-16 So after watching my PSA slowly climb from the nadir at 1.45 on 12/19/16, 2017 was a year of steady increases and a bunch of therapies tried, and failed. After my first chemo session of 6 cycles from 7/18/16 thru 10/31/16, along with 3 month Lupron shots and Zometa
PSA 1124, Age 59, Stage 4, Dx 3-22-16 So after watching my PSA slowly climb from the nadir at 1.45 on 12/19/16, 2017 was a year of steady increases and a bunch of therapies tried, and failed. After my first chemo session of 6 cycles from 7/18/16 thru 10/31/16, along with 3 month Lupron shots and Zometa
ontheroad589
in
Advanced Prostate Cancer
6 years ago
New to this forum
Hello I'm 54 years old. I have relapsing remitting MS for 17 years. I am on Rebif
Hello I'm 54 years old. I have relapsing remitting MS for 17 years. I am on Rebif
Linda243
in
My MSAA Community
6 years ago
High AST levels
Hi, ive been taking rebif rebidose since January and my liver enzymes are high. What is the next best course of therapy since i now know rebif is not for me? Thanks.
Hi, ive been taking rebif rebidose since January and my liver enzymes are high. What is the next best course of therapy since i now know rebif is not for me? Thanks.
Muchomonty
in
My MSAA Community
6 years ago
Stomach, ribs, breast & ear (all in one)
Hello all In February i started having a flareup. My fingers became very painful, i had diarrhoea, so i contacted my dr who immediately asked me to come into hospital and be admitted for a flolan infusion. I already had an appointment to have the infusion at the day unit (SMDU) Manchester. My experience
Hello all In February i started having a flareup. My fingers became very painful, i had diarrhoea, so i contacted my dr who immediately asked me to come into hospital and be admitted for a flolan infusion. I already had an appointment to have the infusion at the day unit (SMDU) Manchester. My experience
ijeasike
in
LUPUS UK
7 years ago
Please i need advice
I have been very unwell nearly a month and am waiting patiently for my flolan infusion. But am struggling so much with my dry mouth down to my throat is dry, painful and tight. This mean that i have lost my voice. The voice loss can come anything. But lately under my neck is swollen. My mouth is so dry
I have been very unwell nearly a month and am waiting patiently for my flolan infusion. But am struggling so much with my dry mouth down to my throat is dry, painful and tight. This mean that i have lost my voice. The voice loss can come anything. But lately under my neck is swollen. My mouth is so dry
ijeasike
in
LUPUS UK
7 years ago
Really???
REALLY!! Each year an individual is diagnosed, at alarming numbers, with multiple sclerosis known as MS. Many often fear or even wonder what this diagnosis brings, other than how celebrities like Montel Williams describe his symptoms. When I was diagnosed I didn't know or understand what multiple sclerosis
REALLY!! Each year an individual is diagnosed, at alarming numbers, with multiple sclerosis known as MS. Many often fear or even wonder what this diagnosis brings, other than how celebrities like Montel Williams describe his symptoms. When I was diagnosed I didn't know or understand what multiple sclerosis
crystaljarvis15
in
My MSAA Community
7 years ago
Not the best of times
Hi all! If have noticed in my last response to Coco about my feet pain, i have been struggling. I took my son out for his birthday last Saturday and that took abit out of me. Then Sunday i was so keen on houvering the house. Since i have been trying out my new light weight houver. I also helped my son
Hi all! If have noticed in my last response to Coco about my feet pain, i have been struggling. I took my son out for his birthday last Saturday and that took abit out of me. Then Sunday i was so keen on houvering the house. Since i have been trying out my new light weight houver. I also helped my son
ijeasike
in
LUPUS UK
7 years ago
Living with MS
I was diagnosed with Ms in 2012. I was on the Medication Rebif and had to change because it was not working for me. Now I'm on Gilenya and it seems to be working for me. My neurologist put me on Ampyra to help with my walking also. It seems that the Ampyra assistance program was terminated Dec.
I was diagnosed with Ms in 2012. I was on the Medication Rebif and had to change because it was not working for me. Now I'm on Gilenya and it seems to be working for me. My neurologist put me on Ampyra to help with my walking also. It seems that the Ampyra assistance program was terminated Dec.
SBLinda
in
My MSAA Community
7 years ago
Flolan
Hi can anybody help With the Flolan treatment I have just had a five day course at the local hospital as a inpatient The Question i have ' is Does anybody have this as a outpatient . Its all pretty new to me . The first year of Crest and Raynaurds. I'm hoping that i can do this as outpatient in the
Hi can anybody help With the Flolan treatment I have just had a five day course at the local hospital as a inpatient The Question i have ' is Does anybody have this as a outpatient . Its all pretty new to me . The first year of Crest and Raynaurds. I'm hoping that i can do this as outpatient in the
Psg83
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Worried sick about my PIP mobility rate been taken
Hi all I just want to know how anybody has coped with the pressure of being in benefit. I want to be healthy again, get a job and become independent. But whenever i try to explore or practice that independence, i have to look over my should incase someone goes to report me that i am not disabled enough
Hi all I just want to know how anybody has coped with the pressure of being in benefit. I want to be healthy again, get a job and become independent. But whenever i try to explore or practice that independence, i have to look over my should incase someone goes to report me that i am not disabled enough
ijeasike
in
LUPUS UK
7 years ago
Flolan infusion
Has anyone had flolan infusion to dilate blood vessels, and if so how effective is this treatment.
Has anyone had flolan infusion to dilate blood vessels, and if so how effective is this treatment.
Marthab
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Secondary Progressive
1st diagnosed with RRMS 2009 have used Copaxone Rebif and now Avonex. Have been told by doctor that we are now looking at Secondary Progressive. He is not yet changing Medication and I have next appointment in Jan 2018. Currently on Avonex. I feel that Avonex is not a correct Medication. What have others
1st diagnosed with RRMS 2009 have used Copaxone Rebif and now Avonex. Have been told by doctor that we are now looking at Secondary Progressive. He is not yet changing Medication and I have next appointment in Jan 2018. Currently on Avonex. I feel that Avonex is not a correct Medication. What have others
chickadee59
in
My MSAA Community
7 years ago
1
...
7
8
9
...
11
Next page
10
Filter results
Clear filters
Posted in
All communities
Advanced Prostate Cancer
64 results
My MSAA Community
55 results
Prostate Cancer Network
37 results
View top 10 communities
Sort by
Most Relevant
Newest