Shingles

I'm on my 3rd divorce we've been apart for 13+ yrs. married 24. He purchased this foreclosure home said I could fix it up and live in it. Use his benefits when he passed, he lives with his gf for 13 yrs. This past Nov. I was blindsided by divorce pprs claiming I owe him all this money, he claims he's in debt he's taken out multiple loans & credit cards he took out most of the equity in the house I'm fixing up. In our state I'm responsible for half his debts. I'm on a low fixed income .
Also I have been following the Ukraine war. Sending messages of hope praying for them. Then I get these guys pretending they are soldiers sending pics trying to romance me then asking for money. I know about scamming I don't fall for it. I feel like I have this big bulls eye target on my back. Why does me caring cause all the nasty people to show up?
#ADHD #Anxiety #Fibromyalgia #Cronic Fatigue# #Osteoporosis #Osteopenia #Raynard syndrome #Peripheral neuropathy #Gout #Shingles

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Hi, my name is LUVMYNYX2. I'm here because I've been suffering from Fibromyalgia and Syringomyelia for over 10 years. My day starts with waking up feeling very stiff in my whole body. It feels like Rega Mortis is setting in. I force myself up feeling tired all the time. My right arm is the most painful, a burning, stinging, scrapping feeling. Very tender to the touch. It feels like the way Shingles is described, except without a rash. Then there is pain around my ribs and pressure in the middle of my spine. It feels like a dagger is in my back. Sore breast too. This pain is every day all day. I work and drive all day and every bump in the road intensify the pain. I take Lyrica 200mg three times a day along with over 1100mg of acetaminophen and Ibuprofen. I get very little relief with that. Doctors have no idea how much hell I'm going through with this horrid pain. When the pain is more intense it raises my blood pressure to stroke range and I don't have high blood pressure. My treatment has been consisted of dry needles on top of my shoulders, vitamin injections in my hands were the worst treatments and very painful. I've had physical therapy 4 times. I was taking also units of Vitamin D three time a week and 2500 of Vitamin B12 3 times a day for pain and protection of my liver and kidneys. Doctor's are only concerned with not giving opioids to protect their licenses while I suffer but yet there is treatment for substance abusers still being served Meth to avoid the issues they go through, I'm not drug addicted, don't want to be high or out of my mind. I just want somebody somewhere to treat my pain so that I can live my life. All I do is work and off to the bed. I have to work with prices getting higher and higher. I'm only 67 and feel bad when my grandchildren want me to do things with them. I also have asthma and stays out of breath here lately. Thanks for listening.

#MightyTogether #Fibromyalgia

FATIGUED OR WHATEVER

Hi, my name is Podiceps73. I'm here because I have been very active all of my life and enjoyed outdoors immensely. And now things have changed. And no one can put a finger on exactly what has happened- but a few people have their opinions which is all that they are.

In January 2022, I received my booster injection for Covid 19. Within three days I developed a slight rash on my abdomen. Two days later it was confirmed that I had Shingles. I was 72 years old and was ignorant of the need to be double immunised and my Doctor (who is a dedicated physician) failed to see the warning on my health pages. I had Shingles twenty five years earlier so never thought of it recurring. The latest Shingles rash passed and no more skin pain occured. I had moderate pain and a rash of about 50mm diameter on my LHS abdomen and a few spots on the side and back.

A fortnight later I was finding it difficult to speak normally and when I did speak I was so slow getting the right words out that it was becoming a serious concern to say the least. My movements had also slowed down and we described at as the speed of an old sloth- I was truly very very slow. I was checked out by the local Hospital ED and no identifiable issues found.

Two or three weeks later I was referred to a Regional ED with suspected mini-strokes. I spent three nights in hospital and a thorough assessment occured including MRI of my brain. Still nothing found. One prior experience that I had was videod to show the Doctors just what was happening. I was sitting in a lounge chair reading and I had my legs crossed. I thought I will put them straight- in other words my intention was to lift my right leg off my left leg. Pretty simple procedure. We normally just automatically get on with it. But for some reason try as I might, I could not lift my right leg for even one millimetre- it was stuck there for about 15 minutes.
By this time I was wondering if this was just a load of "it's all in your head" stupid! But I sensed that it was real. This became my new reality and I had repeated episodes.

When I walked my legs felt as if they weighed a tonne and I could at best shuffle along; my arms also just hung heavily and required a bit of mental assistance to be lifted; my turning movements were slow just like a sloth- lifting my arms and legs required planning because my automatic functions had stopped working. I wondered if there was one part of my brain wanting to move and the other normally responding part failing to coperate.

The next four months saw the arrival of new changes that suggest I have to get used to this long term. And still no one has an answer.

If you've been working through your own chronic pain for a while now – what would you tell someone who's just been diagnosed that you wish you had known?

I'll start...

I wish someone had told me to NEVER compare myself to others who were also sick. Pain management looks different for everyone. #ChronicPain #Neuropathy #neuralgia #ComplexRegionalPainSyndrome #Fibromyalgia #Nervedamage #MultipleSclerosis #Arthritis #Shingles #Migraines #BackPain #Cancer

Once again I woke up nothing but shooting chronic pain on top of all this bone internal pain shingles have have got me burning inside and out I don't know if I can take it anymore #ChronicPain #Shingles #Suicide

Have been having Shingles outbreaks for the last 2 years…now on my 4th attack. So painful. Wonder if it is connected to Lymes?