Search
Search
About
Log in
Join
Experiences with
Head pain
Posts
Communities
14,372 public posts
Filter results
Anyone elses bones absolutely ache??
One of my recurring pains at the moment has been aching bones. It feels like the centre of all my bones (mostly arms, fingers and legs) has this deep rooted numbing pain and I'm at such a loss with it. Someone with fibromyalgia has noticed a few things about how I am and thinks I have fibro as well
One of my recurring pains at the moment has been aching bones. It feels like the centre of all my bones (mostly arms, fingers and legs) has this deep rooted numbing pain and I'm at such a loss with it. Someone with fibromyalgia has noticed a few things about how I am and thinks I have fibro as well
ArtyPal
in
Endometriosis UK
2 years ago
What else is available?
I have done Carbo/Taxol, Avastin, Carbo/Caelyx, Rubrac a and now Anastrazole. I have a scan coming up, but lately can feel the cancer spreading and am resorting to pain killers. Can anyone who has had this many lines of chemo tell me what else was available for them to try, and also how successful it
I have done Carbo/Taxol, Avastin, Carbo/Caelyx, Rubrac a and now Anastrazole. I have a scan coming up, but lately can feel the cancer spreading and am resorting to pain killers. Can anyone who has had this many lines of chemo tell me what else was available for them to try, and also how successful it
27-359
in
My Ovacome
2 years ago
Please help. Do you suffer from any of these?
Sometimes I get a shooting
pain
through my temples in my
head
making me squint. When I'm sitting down, I always have to either move my fingers or my feet. Always have shaky hands. Doctors don't think it's anything neurological.
Sometimes I get a shooting
pain
through my temples in my
head
making me squint. When I'm sitting down, I always have to either move my fingers or my feet. Always have shaky hands. Doctors don't think it's anything neurological.
greysanatomy1
in
Pain Concern
1 year ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Flow diverter op.
I had a ruptured aneurysm in 2018 which I had coiled, but have had
head
pain
since, but accepted that as side effects along with short term memory probs, processing and daily life stuff.. But now I have another and the surgeons want to fit a flow diverter to seal this area off š¤š¤·āāļø..
I had a ruptured aneurysm in 2018 which I had coiled, but have had
head
pain
since, but accepted that as side effects along with short term memory probs, processing and daily life stuff.. But now I have another and the surgeons want to fit a flow diverter to seal this area off š¤š¤·āāļø..
Purplepop
in
Neuro Support
2 years ago
Mental Health and Endometriosis
I have read books about endo I change diet, I start meditation even tried do yoga but unfortunately
pain
is every where, kidney, abdominal ,leg ,hand,
head
..back so can't do even daily routine without sweating and
pain
.
I have read books about endo I change diet, I start meditation even tried do yoga but unfortunately
pain
is every where, kidney, abdominal ,leg ,hand,
head
..back so can't do even daily routine without sweating and
pain
.
JustLiLi
in
Endometriosis UK
1 year ago
Lip Biopsy - Is a lack of/missing saliva glands a āthingā?
Hello, I wonder if anyone can advise me. Iāve struggled with worsening sicca symptoms for years, the dry eyes from childhood. In the midst of a long and bad flare, I eventually got referred to a ālupusā rheumatology clinic, following a weak pos ANA and speckled IgG, blood result. This was as Covid hit
Hello, I wonder if anyone can advise me. Iāve struggled with worsening sicca symptoms for years, the dry eyes from childhood. In the midst of a long and bad flare, I eventually got referred to a ālupusā rheumatology clinic, following a weak pos ANA and speckled IgG, blood result. This was as Covid hit
UrsaP
in
Sjogren's Support
2 years ago
Elreada: minimal effective dose
As a metastatic G9 5+4 I have always cared more (unless
pain
ever has a gun at my
head
) about QOL. in 2012 when I was diagnosed with 5 bone spots on my pelvis I was up for surgery or radiotherapy but was sent away with a zoladex prescription. It would be different if i was diagnosed now.
As a metastatic G9 5+4 I have always cared more (unless
pain
ever has a gun at my
head
) about QOL. in 2012 when I was diagnosed with 5 bone spots on my pelvis I was up for surgery or radiotherapy but was sent away with a zoladex prescription. It would be different if i was diagnosed now.
Rickytarr
in
Fight Prostate Cancer
1 year ago
Fibromyalgia and Lisfranc
In one way it was a relief because I honestly though I was going round the bend and I think my family though pt it was all in my
head
eg headaches, joint
pain
, confusion, forgetfulness, tired all the time not to mention losing my balance and falling but I think this was primarily due to me being tired
In one way it was a relief because I honestly though I was going round the bend and I think my family though pt it was all in my
head
eg headaches, joint
pain
, confusion, forgetfulness, tired all the time not to mention losing my balance and falling but I think this was primarily due to me being tired
Hamer5
in
Fibromyalgia Action UK
2 years ago
Aches and Pains
I came off Rubraca in November, and since then have developed severe back ache. It hurts when I walk, sit and when I am in bed, but not continually! I am having a scan in a couple of weeks as the oncologist thinks it could be lymph node involvement behind my spine. I have been given Oramorph for pain
I came off Rubraca in November, and since then have developed severe back ache. It hurts when I walk, sit and when I am in bed, but not continually! I am having a scan in a couple of weeks as the oncologist thinks it could be lymph node involvement behind my spine. I have been given Oramorph for pain
27-359
in
My Ovacome
2 years ago
Round ligament pain first trimester
Is that round ligament
pain
? Iām trying to not over dramatise in my
head
or Iāll worry Iāve torn or done something to the baby š Iām 10 weeks x
Is that round ligament
pain
? Iām trying to not over dramatise in my
head
or Iāll worry Iāve torn or done something to the baby š Iām 10 weeks x
PrincessGurn1984
in
Fertility Network UK - Pregnancy Support
1 year ago
Pain medication recommendations for knee & ankle swelling & inflammation
I find that swelling in either of my knees or ankles triggers my RLS. Since I had a knee replacement 6 months ago, the swelling happens frequently as both legs readjust to the post-surgical healing. A new study revealed that ibuprofen and other NAISDS can cause fatal kidney disease, so my GP took me
I find that swelling in either of my knees or ankles triggers my RLS. Since I had a knee replacement 6 months ago, the swelling happens frequently as both legs readjust to the post-surgical healing. A new study revealed that ibuprofen and other NAISDS can cause fatal kidney disease, so my GP took me
Bganim1947
in
Restless Legs Syndrome
2 years ago
Help/advice about periods please!
I'm messaging here because I've been dismissed by male doctors before and I'm not sure whether to make an appointment or not. I've basically always had irregular periods but they've been getting worse and worse - heavier and more painful and I can never predict when I'll get it. Cycle length varies
I'm messaging here because I've been dismissed by male doctors before and I'm not sure whether to make an appointment or not. I've basically always had irregular periods but they've been getting worse and worse - heavier and more painful and I can never predict when I'll get it. Cycle length varies
Lizardelle
in
Women's Health
2 years ago
Updated
I have been on benepali for 5 weeks and I am feeling it working at last! I am not in as much pain as I was 5 weeks ago. I am only taking one lot of pain killers a day and sometimes 1 naproxen, so much improved. My fatigue has nearly gone. It only comes back when I do too much or on a Friday before my
I have been on benepali for 5 weeks and I am feeling it working at last! I am not in as much pain as I was 5 weeks ago. I am only taking one lot of pain killers a day and sometimes 1 naproxen, so much improved. My fatigue has nearly gone. It only comes back when I do too much or on a Friday before my
Carolsos
in
NRAS
2 years ago
Short Frenulum
I can expose the
head
of my penis when flacid and erect. I have no
pain
when peeing or with erections. However, it isn't particularly natural for me to pull it back when masturbting etc. and the foreskin always rolls back so only around half of my glans are exposed when i do pull it back.
I can expose the
head
of my penis when flacid and erect. I have no
pain
when peeing or with erections. However, it isn't particularly natural for me to pull it back when masturbting etc. and the foreskin always rolls back so only around half of my glans are exposed when i do pull it back.
healthhelp12
in
Men's Health Forum (Penis Health)
1 year ago
Private GP to get NHS referral
Hi Ladies I hope you are doing as well as it can be A quick question and a few background notes. Suffering from pain for 10 years. The pain got stronger over time and now lasts longer. Last couple of years in particular were the worst. So far I couldnāt get even the right painkillers from my gp but
Hi Ladies I hope you are doing as well as it can be A quick question and a few background notes. Suffering from pain for 10 years. The pain got stronger over time and now lasts longer. Last couple of years in particular were the worst. So far I couldnāt get even the right painkillers from my gp but
Thisisme-
in
Endometriosis UK
2 years ago
Sciatica/nerve pain when walking - what do I do next?
I am getting tired of this pain - and the pain does cause fatigue. To give context, I started getting sciatica in 2020. I thought it was due to less movement because of COVID. Over the couple of years, itās got worse, in addition to elongated, irregular periods and brown spotting. I canāt walk without
I am getting tired of this pain - and the pain does cause fatigue. To give context, I started getting sciatica in 2020. I thought it was due to less movement because of COVID. Over the couple of years, itās got worse, in addition to elongated, irregular periods and brown spotting. I canāt walk without
Catinboots
in
Endometriosis UK
2 years ago
Shaking hands
Hi I have been diagnosed with peripheral neuropathy plus I have RA orRD and I have posted on here before.Iām struggling with both conditions now. Iām only on methotrexate plus the occasional pain pills. The peripheral is bad enough but the hand tremors now are exhausting and I donāt feel well most
Hi I have been diagnosed with peripheral neuropathy plus I have RA orRD and I have posted on here before.Iām struggling with both conditions now. Iām only on methotrexate plus the occasional pain pills. The peripheral is bad enough but the hand tremors now are exhausting and I donāt feel well most
orange33
in
Neuropathy Support
2 years ago
Ovaries & tubes removed- 3 days post op
Hey, So Iāve finally had my op after it being cancelled the first time. Was in surgery longer than expected. Iām 3 days post op, yesterday was a pretty good day, today already feels like a really bad day. I was told after surgery I am not allowed my HRT back due to abdominal growths they had to remove
Hey, So Iāve finally had my op after it being cancelled the first time. Was in surgery longer than expected. Iām 3 days post op, yesterday was a pretty good day, today already feels like a really bad day. I was told after surgery I am not allowed my HRT back due to abdominal growths they had to remove
JH21
in
Endometriosis UK
2 years ago
Started Peginterferon!
Started well five weeks ago with no side effects but now am suffering from a lot of
pain
in my arms, back and
head
and other odd places. My question to you all good folk is āshould I stick with it for a little longer?ā
Started well five weeks ago with no side effects but now am suffering from a lot of
pain
in my arms, back and
head
and other odd places. My question to you all good folk is āshould I stick with it for a little longer?ā
Fairbank
in
MPN Voice
2 years ago
struggling to see the point in anything, just want to join my mum.
I know there are people worse off but they donāt live in my
head
, i do.
I know there are people worse off but they donāt live in my
head
, i do.
Mimsyblue
in
Anxiety and Depression Support
1 year ago
1
...
69
70
71
...
100
Next page
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Endometriosis UK
2620 results
Fibromyalgia Action UK
1335 results
NRAS
972 results
View top 10 communities
Sort by
Most Relevant
Newest