It is a point of contention between my husband and I because I tend to snap at him, but I don't mean to and I try to help him understand that that it is neither his fault nor mine. It just is. Please tell me that I am not the only one with fibromyalgia who is easily startled!!
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Anyone Brits finding themselves kicked off the NHS list at their dentists in England? And given no warning?
I've heard there was a shortage, but this is ridiculous. The costs of private treatments are so high 😭
And no plans from the government to sort it out 🙄
Literally no dentist is taking new NHS patients and if you were on a list -quickly check if you haven't been kicked off!
www.google.com/amp/s/amp.theguardian.com/society/2022/may/24...
#nhs #dentist #nhsdentist #Asthma #ChronicFatigue #Fibromyalgia #FunctionalNeurologicalDisorder #IrritableBowelSyndromeIBS #Depression #Anxiety #occasional agoraphobia #BackPain #Overactive bladder
Anyone with Interstitial cystitis, what did it take for you to be finally diagnosed?
Had 6 courses of antibiotics, the current course is meant to last for 3 months.
Been a couple of weeks, but still dealing with: incontinence, taking ages to pee, intense and debilitating bladder pain... Exhaustion
My body is knackered and I really don't feel like the antibiotics are helping 😭
...and if I have to drink another cup of cranberry juice I'm going to hurt someone lol.
The Urologist discharged me with the latest batch of antibiotics and a quick fat shame (thanks doc 🙃).
Terrified about being fired from my job and failing my uni course 🙁
#InterstitialCystitis #BladderIncontinence #Overactive bladder #ChronicPain #Fibromyalgia #ChronicFatigue #AuditoryProcessingDisorder #Depression #Anxiety #IrritableBowelSyndromeIBS
FND enter my life in 2008, I wasn’t diagnosed until 2010 and I have dealt with many different types of symptoms, but these past few months have been hitting me pretty hard. In 2017 I woke up with my toes curled inwards. Long story short, I haven’t walked in two years, now I am getting hit hard with multiple symptoms, #severeendometriosis (on a wait list for surgery), ringing in my left ear (#Tintinitus ) since 3/25/2020, UTI for the whole month of May and I have been symptomatic every since. Had a ultrasounds of my pelvis bladder and my bladder/kidneys, waiting on my results (PCP, said it was #overactedbladder ). This is too much.
I have been dealing with a health problem for ten years without any diagnosis. I have seen so many doctors, spend a lot of money and have gotten no where. I ignored it, as I can go months between flare ups. But when it does flare, it is incredibly uncomfortable. This is a bladder problem, by the way. There are three possibilities; #InterstitialCystitis #PelvicFloorDysfunction #Overactive bladder . However, due to the other symptoms I feel in addition to the frequency make me believe it isn’t overactive bladder. The doctor I saw today seemed far too eager to dismiss the rest of my symptoms and my ten years of discomfort. Ten years of missing out on life because I need a bathroom everywhere I go. Ten years of missing road trips with friends. All my hopes that this doctor could help me went right out the window when he went straight to asking if I wanted him to write me a prescription for overactive bladder meds without any exam or diagnosis. I’m so upset by this and I’m feeling hopeless and no closer to a solution. What am I to do? I have a difficult time even working. How am I supposed to just live this way?
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