Experiences with

Deep heat

Severe Pain in Right Hand Although not completely free of pain, the combination of Deep Heat & Valtarol Gel, mixed together, and rubbed in has relieved the pain by about 70%. instead of the pain being across the whole hand it is now concentrated around the thumb I have had a couple of chats

Interestingly, whilst recently in Australia, I asked a Pharmacist if he had anything he could give me to ease the pain, he suggested mixing Deep Heat and Voltarol together and rubbing that into the hand, although it has not stopped the pain completely, it has reduced the area of pain to the region of

Went to see the doctor 6 weeks ago and he told me to take paracetamol and deep heat!! After two weeks of popping paras (which may have increased liver damage? See later in post) no change so i went back to see a helpful doc who reduced statins and bisoprol dosage.

Deep heat relieves the pain in my shoulders and upper arms but only lasts about an hour or so. I take cocodamol 30mg but they don’t help. I am on blood thinners so can’t take ibuprofen. Do you have any advice?

I took two ibuprofen, rubbed some deep heat on my shoulder and went back to bed. Woke the next day with only a bruised feeling in my heart. Walked about the entire day feeling a bit odd with the bruised heart. Eventually dialled 111 and was told to go to A and E.

Salt pool, deep heat .

The only thing that helps is heat - Deep Heat or a hot water bottle. I'm stiff, and the pain can be sharp if I cough, or move too quickly. Sorry for three paragraphs before the question - could this be a PMR flare?

I have purchased some Deep Heat muscle rub thinking it would help my aches and pains, but on the leaflet enclosed it states that people taking anticoagulants should not use it owing to the ingredients interacting with this medication. I take Warfarin.

Question is , since being on the medicine, I am constipated headaches, sickness, dizzy, tired, fed up, and now when i take my vitals, even before i take my meds in morning and eve, my bp is 102/63 my heart rate is 59 - 61, my heart rate and bp makes me so cold like a deep freeze which gives me light

My legs are jumpy in the evening, I use loads of 'Deep Heat' on them every evening and they are interfering with my sleep as my calf's keep cramping when I am in bed. Even putting a Tens device on them does not help much.

I don't take tablet form medication but use heat and salt baths but I am really struggling. Any tips or over the counter rubs for muscles I've tried deep heat voltral the usual suspects I don't feel they work

He took paracetamol & used Bio Freeze, similar to deep heat. He got progressively worse, a GP diagnosed Frozen Shoulder over the phone, prescribed Co-Codamol & Naproxen. Within days he was in a state of collapse, couldn’t walk and lost a lot of weight.

What else can I do , I use a deep freeze gel but that’s not doing anything to help tonight 😢😢😢

But nothing a pain killer and deep heat can sort. I'm joining a park run group this Saturday so running with other people should be a big help I hope. Tho don't mind on my own as earbuds and music. Not had wee 👁️ eye op yet hope it's soon. Well hope your all doing well. Love to all..❤️❤️❤️x

had DBS five years ago lately my left arm which worse affected side feeling numb and has electrical feelings. any one has the same? What could it be?

I’ve tried everything exercise, diet, CL, DBS. Cl does not help at all. DBS does not help. I have dystonia on my right side. Constant pain in my shoulder, hip, and feet. This is the end. Don’t tell me to think positive!! I’m begging God to take me now. My poor hubby and kids (adult). What can I expect

It's been 3 months since my DBS surgery and 6 weeks since switch on. Since then I've had two follow up conversations with the programmer, both telling me to leave my medication alone and increase the stimulation slowly. Since switch on I've been troubled by severe dyskinesia. Its exhausting. My next

https://www.science.org/doi/10.1126/sciadv.ado4927?fbclid=IwY2xjawJVMGZleHRuA2FlbQIxMQABHRBDa9RJWMGOFOYxLDnqxNsFaANf9RTriEX2OOQMySm4AdwkZzAJlkgGmg_aem_C7Z_4PXuqgDEIWF8E8v8jg

As a follow up to my recent post...and to recap, 6 months into Tinnitus that started following performing at a gig with excessively loud stage volume....on Mirtazipine for 4 months (hoping to taper off in August) and 10 CBT sessions in...... I currently take care with noise, wear hearing protection

Hi all. You might remember that I recently posted about voice issues. There was a great response which I’m thankful for. However,I think I’ve realised that there are definitely two things at work: one is the PD of course and your possible solutions were pertinent here. Second though is the DBS which