chronic migraine

HoneyJ
Online Community Member Posts: 1 Listener
Looking forward to chatting to others who experience chronic migraine for help, support and advice on how to best cope with the pain and strategies to help prevent them but still have some fun in life 




1
Comments
-
Hello @HoneyJ and a warm welcome to the community. Glad to have you with us. I have had a quick look, and members have discussed chronic migraines previously here, You might find it useful to have a look.
You may also find relevant discussions in the Dealing with chronic pain thread.
Things may be a little quiet today, but bear with us and others will be along in due course to chat to you and share with you
In the meanwhile, if you have any questions you would like to ask or anything more you would like to tell us, please don't hold back. We are here for you.
Warmest best wishes,
Richard1 -
Hi @HoneyJ, welcome to the community!0
-
Welcome1
-
Hi again @HoneyJ, just thought I would introduce you to @sunflower who also has experience with chronic migraines and has recently joined the forum!0
-
Hi @honeyJ welcome!
In the few short days I've been on here I've received more relevant advice and support than I have from anywhere else. You've come to the right place!
I'm really struggling right now with chronic migraine. It's a truly difficult time. Everyone's experience is different.1 -
Hi I’ve been having really bad migraines for about 30 years now and there never seems to be an answer to controling them, when if feel one coming on ( and it all depends on which side of my head it is) i take a tablet or if it’s really bad i have one of my lnjections. I don’t know anyway of controlling them but if anyone has answeres that be good. NC0
-
The user and all related content has been deleted.0
-
Hi everyone. I can totally sympathise with Migraine sufferers. I've had them all my life (in 52 now) but for the last 8 years they have been constant along with cluster headaches! After attending Neurology for 3 years and trying every medication available I was finally referred for BOTOX injections. Every three months, they do help but haven't taken them away altogether. I've had 3 rounds so far and I have to say the last round hasn't helped much at all.... I suffer with other illnesses to, Fibro, JHD, SAI, Hypothyroidism to name a few.... I've been in bed most of this week and have to say sometimes life sucks. Currently waiting to attend Neurology to see if I have MS. Does anyone have MS on here, I'd really like some more info...... #frustrated #fedup......0
Categories
- All Categories
- 15K Start here and say hello!
- 7.1K Coffee lounge
- 83 Games den
- 1.7K People power
- 108 Announcements and information
- 23.6K Talk about life
- 5.5K Everyday life
- 305 Current affairs
- 2.3K Families and carers
- 858 Education and skills
- 1.9K Work
- 504 Money and bills
- 3.5K Housing and independent living
- 1K Transport and travel
- 868 Relationships
- 254 Sex and intimacy
- 1.5K Mental health and wellbeing
- 2.4K Talk about your impairment
- 858 Rare, invisible, and undiagnosed conditions
- 916 Neurological impairments and pain
- 2K Cerebral Palsy Network
- 1.2K Autism and neurodiversity
- 38.4K Talk about your benefits
- 5.9K Employment and Support Allowance (ESA)
- 19.3K PIP, DLA, ADP and AA
- 7.8K Universal Credit (UC)
- 5.5K Benefits and income