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Urgent: Synarel nasal spray! Desperate to sneeze after but holding it in!
Just started Synarel nasal spray today. I took it 10 min ago but now desperate to sneeze and blow my nose!! When can I do either???
Just started Synarel nasal spray today. I took it 10 min ago but now desperate to sneeze and blow my nose!! When can I do either???
Mrs_MT
in
Fertility Network UK
5 months ago
Antihistamines and tinnitus
I have had right sided tinnitus for over 4 months. I have seen ENT, audiology , MRI etc. There are no reasons found for the tinnitus. I am partially habituated but it can lead to loss of sleep at night. However, I get pollen allergies at about this time of year and start taking antihistamine - ceterizine
I have had right sided tinnitus for over 4 months. I have seen ENT, audiology , MRI etc. There are no reasons found for the tinnitus. I am partially habituated but it can lead to loss of sleep at night. However, I get pollen allergies at about this time of year and start taking antihistamine - ceterizine
norcar
in
Tinnitus UK
11 months ago
What comes after, what comes next?
I have posted a few times about my dad. Stage 4, mets to 8+ bones at time of diagnosis, PSA at 137 (10/22.) Lupron twice a year, Bicalutamide, failed at 7 months, Xtandi failed at 4 months, currently on Zytiga. We met with my dad’s oncologist on 4/24. My Dad’s PSA dropped from 2.47-1.46 and pain has
I have posted a few times about my dad. Stage 4, mets to 8+ bones at time of diagnosis, PSA at 137 (10/22.) Lupron twice a year, Bicalutamide, failed at 7 months, Xtandi failed at 4 months, currently on Zytiga. We met with my dad’s oncologist on 4/24. My Dad’s PSA dropped from 2.47-1.46 and pain has
lgutman
in
Advanced Prostate Cancer
5 days ago
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Need to vent to people who will get it.
As the title says. I'm struggling right now and just wanna cry, but can't because I'm on holiday and it's my birthday and I should be having a wonderful time. I had to get a taxi and come back to my hotel around 5pm and haven't moved from the bed since. I feel exhausted. It was only a 20min walk from
As the title says. I'm struggling right now and just wanna cry, but can't because I'm on holiday and it's my birthday and I should be having a wonderful time. I had to get a taxi and come back to my hotel around 5pm and haven't moved from the bed since. I feel exhausted. It was only a 20min walk from
Diagnosis_Collector
in
LUPUS UK
10 days ago
Had my nasal surgery, in mom's house
My nose doesn't stop running. Mom was cute but started to trigger me especially when trying to make sis study faster. All day in hospital, no food till 8pm, three times drawn blood, anesthesia, waiting... Wondering when to go back. I don't like both my living options.
My nose doesn't stop running. Mom was cute but started to trigger me especially when trying to make sis study faster. All day in hospital, no food till 8pm, three times drawn blood, anesthesia, waiting... Wondering when to go back. I don't like both my living options.
Against_the_current
in
Anxiety and Depression Support
11 months ago
Another Pred journey
I have been 5 years on Pred and 3 years on Actemra A bit of up’s and downs but did very well with no side effects ( except bone loss) Lately got to 3 and poof back to square one again after major flare. Up to 20 mg with a probable 2 year tapering schedule. Probably same thing will happen again below
I have been 5 years on Pred and 3 years on Actemra A bit of up’s and downs but did very well with no side effects ( except bone loss) Lately got to 3 and poof back to square one again after major flare. Up to 20 mg with a probable 2 year tapering schedule. Probably same thing will happen again below
Sunny1947
in
PMRGCAuk
2 months ago
PEP for asthma
Morning. Due to being immunocompromised …on Rituximab infusion. I keep getting the same chest infection. Had three lots of antibiotics over 4 weeks. I was considering buying a PEP to try and keep my chest clear. Has anyone any advice on which to buy please? TIA
Morning. Due to being immunocompromised …on Rituximab infusion. I keep getting the same chest infection. Had three lots of antibiotics over 4 weeks. I was considering buying a PEP to try and keep my chest clear. Has anyone any advice on which to buy please? TIA
Evie3
in
Asthma Community Forum
2 months ago
Update- transfer confirmed, thinnish lining though
I had a scan today to check to see if some fluid in my uterus had cleared up. At my last scan my lining was 8.6mm and I was put on progesterone and told that my lining would not shrink now. I saw a different Dr today and was alarmed when she said my lining was "6.4mm" she then spent about 2 minutes silently
I had a scan today to check to see if some fluid in my uterus had cleared up. At my last scan my lining was 8.6mm and I was put on progesterone and told that my lining would not shrink now. I saw a different Dr today and was alarmed when she said my lining was "6.4mm" she then spent about 2 minutes silently
Here4ivfinfo
in
Fertility Network UK
2 months ago
Bronchiectasis .. currently using Aerobika .. but just wondering has anyone / does anyone use the Evergreen Pari-o-pep mucus clearing device
Hi Has anyone tried the above device?..I get on ok with my aerobika but wondering if it’s worth spending £35 on the Evergreen Pari -o Pep? If it speeds things up I’d be interested in buying one 🙏
Hi Has anyone tried the above device?..I get on ok with my aerobika but wondering if it’s worth spending £35 on the Evergreen Pari -o Pep? If it speeds things up I’d be interested in buying one 🙏
Phill1
in
Lung Conditions Community Forum
3 months ago
Latest COVID-19 guide for immunocompromised blood cancer patients from the International COVID-19 Blood Cancer Coalition (ICBCC)
The latest Patient Impact Statement has been released by the International COVID-19 Blood Cancer Coalition (ICBCC). Titled [i]"Navigating a post-pandemic world: A guide for immunocompromised blood cancer patients"[/i], it aims [i]"to help you navigate and manage the risks arising from the combination
The latest Patient Impact Statement has been released by the International COVID-19 Blood Cancer Coalition (ICBCC). Titled [i]"Navigating a post-pandemic world: A guide for immunocompromised blood cancer patients"[/i], it aims [i]"to help you navigate and manage the risks arising from the combination
CLLerinOz
Volunteer
in
CLL Support
3 months ago
constipation!!!
Hello anyone I have got this constant gnawing ,scratching ,pinching ETC going on in my bum and for 3/4 months really bad constipation frightened to poop in case I "UNBLOCK" myself to the nasty stuff I just can't control I looked it up on DR GOOGLE and it came up with Proctalgia Fugax/ Levator Syndromeas
Hello anyone I have got this constant gnawing ,scratching ,pinching ETC going on in my bum and for 3/4 months really bad constipation frightened to poop in case I "UNBLOCK" myself to the nasty stuff I just can't control I looked it up on DR GOOGLE and it came up with Proctalgia Fugax/ Levator Syndromeas
bungi1961
in
Bowel Disease Support
4 months ago
polymorphic eruption of pregnancy
Hi I am 6dp5dt. From the beginning I noticed a rash in lower part of abdomen. It was later appeared also near belly button (then disappeared), then under breast (then disappeared) and the only mark left is the lower abdomen one. Reading online made me realize it might be associated to PEP (or PUPPP
Hi I am 6dp5dt. From the beginning I noticed a rash in lower part of abdomen. It was later appeared also near belly button (then disappeared), then under breast (then disappeared) and the only mark left is the lower abdomen one. Reading online made me realize it might be associated to PEP (or PUPPP
super_ano
in
Fertility Network UK
5 months ago
Update: post-radiation and New meds
Hello Friends and warriors! Dragonfly is updating the latestest treatment... Radiation to the sacrum and L5 (10 treatments) ended on Dec 4th but since then I've had a rollercoaster of side effects...mostly stiffness and muscle spasms that catch me unawares when I get up or sit down. I truly thought
Hello Friends and warriors! Dragonfly is updating the latestest treatment... Radiation to the sacrum and L5 (10 treatments) ended on Dec 4th but since then I've had a rollercoaster of side effects...mostly stiffness and muscle spasms that catch me unawares when I get up or sit down. I truly thought
Dragonfly2
in
SHARE Metastatic Breast Cancer
5 months ago
Anxiety
I suffer from bad anxiety, and PTSD from childhood to now, and am 61 years old. I'd like to join this group to see what others do, or get new ideas on helping with these issues. I do mindfulness and breathing techniques, adult coloring. Can't do a lot of exercises because of DDD, and other back problems
I suffer from bad anxiety, and PTSD from childhood to now, and am 61 years old. I'd like to join this group to see what others do, or get new ideas on helping with these issues. I do mindfulness and breathing techniques, adult coloring. Can't do a lot of exercises because of DDD, and other back problems
Tacoblue
in
Anxiety and Depression Support
3 days ago
Sertraline for PTSD symptoms
hi, I’m new to this forum - usually post on NRAS forum, as I have Rheumatoid arthritis. but I also have long history of trauma, PTSD/CPTSD.. last year has got particularly worse (albeit my RA meds have also severely impacted me mentally) I’m going through incredible amounts of stress atm and my
hi, I’m new to this forum - usually post on NRAS forum, as I have Rheumatoid arthritis. but I also have long history of trauma, PTSD/CPTSD.. last year has got particularly worse (albeit my RA meds have also severely impacted me mentally) I’m going through incredible amounts of stress atm and my
Sapphire1701
in
Heal My PTSD
7 days ago
new user
hey everyone- not really sure how this works but I’m a 40 y/o lgtbq female whose been diagnosed as bipolar, depression, ptsd, anxiety, etc—- mostly bc I haven’t responded to any of the treatments I’ve received over the past 2 decades. Currently unemployed in the mental health field. Don’t have much
hey everyone- not really sure how this works but I’m a 40 y/o lgtbq female whose been diagnosed as bipolar, depression, ptsd, anxiety, etc—- mostly bc I haven’t responded to any of the treatments I’ve received over the past 2 decades. Currently unemployed in the mental health field. Don’t have much
So_It_Goes
in
Anxiety and Depression Support
15 days ago
Sensory Processing and PTSD
I found this article really interesting (yet to read it all, initially attracted to images): https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2021.625490/full
I found this article really interesting (yet to read it all, initially attracted to images): https://www.frontiersin.org/journals/neuroscience/articles/10.3389/fnins.2021.625490/full
Lady4
in
Functional Neurological Disorder - FND Hope
17 days ago
a beautiful practice
over the years I have done yoga in many different studios but it did very little for me. Before ptsd it was the key to my happiness, and after my body was too tense and stuck in fight or flight to let the postures in. This kind of yoga is what I need. Enjoy https://www.youtube.com/watch?v=wCJfXwm97rw
over the years I have done yoga in many different studios but it did very little for me. Before ptsd it was the key to my happiness, and after my body was too tense and stuck in fight or flight to let the postures in. This kind of yoga is what I need. Enjoy https://www.youtube.com/watch?v=wCJfXwm97rw
Agara33
in
Heal My PTSD
27 days ago
Many years after lithium toxicity
Is there anything to treat neurological problems and PTSD caused by long-term effects of lithium toxicity ?
Is there anything to treat neurological problems and PTSD caused by long-term effects of lithium toxicity ?
petersurvivor
in
Headway
1 month ago
Hopelessness
I've been diagnosed officially with PTSD this week which is not a shock. I begin EMDR sessions next week so hope those are able to help. I have these bouts of feeling hopeless. I'm trying not to go too hard on myself but just feel that things will never get easier. Cry myself to sleep most nights with
I've been diagnosed officially with PTSD this week which is not a shock. I begin EMDR sessions next week so hope those are able to help. I have these bouts of feeling hopeless. I'm trying not to go too hard on myself but just feel that things will never get easier. Cry myself to sleep most nights with
Hidden
in
ICUsteps
1 month ago
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