Guest guest Posted July 16, 2006 Report Share Posted July 16, 2006 Tracie...Thanks for the informations. Again I will be saving it for future reference. I picked up shoe inserts for the Plantar Fasciitis Thursday and since they are hard material it seems to be making them worse. Going to call them tomorrow. I've been waiting for several weeks for these. Is there anything that helps? It is really bad first thing in the morning. I've been doing stretching. My primary care says sometimes a difficult case need to be cast, but if it is the sarc would that really help. thanks again Ruth > > In a message dated 7/11/06 11:19:54 PM Pacific Daylight Time, > olehomepla@... writes: > > > > What do you mean by " hard > > muscles " in your back? I have been struggling for a while with > > morning back pain in the large muscles between my shoulder blades > > and my lower back...and have been told it is Fibro. Are these the > > same muscle you are talking about? > > For me, all the muscles thru my back and chest are like concrete. I can > exercise, and initially- they get " more solid " or " pumped up " as body builders > would want them to become. But for me, they don't soften up--even after an hour > massage. they are so atrophied that any small injury becomes a huge problem. > This is what sarcoidosis does to muscles and ligaments. It takes the > " elasticity " away. I can run my hands down my arms, and feel the granulomas down my > forearms, and you can visually see the lumps. > In the lymphs-- mine feel like a " land mine. " Depending on where the > inflammation of the day decides to settle, it can be a constant problem spot, or it > can come and go. Unlike a cyst, where you can generally feel the free floating > sac-- these are anchored--and when the flare is really in its nasty stage-- > its a bitch. > I am learning what makes mine more severe--dairy and refined sugars and > dehydration. So I've been cutting the dairy out of my diet- going with Rice Dream > for cereal, and non-dairy yoghurts, Almond or Soy Milks, but soy is difficult > to digest. > I also swear by Milk Thistle tea and capsules, MSM powder for muscle and > joint pain (no condrontin (sp)). My liver enzymes and Liver function tests are > all normal now, and I don't get as much of the lactic acid buildup that I was > suffering from since I cut out the dairy. > Also, since I'm not gorging on dairy, I can take a small amount of > calcium/magnesium and not have a problem with it. > > I too have CT, but I never > realize that it could be from the Sarc nor has > > anyone mentioned it. I now am dealing with Platar Fasciitis...is this more > > granduloma too? This is one thing I'm not too familar with-- Plantar > > Fasciitis that is. What they do know is that sarcoidosis loves feet and hands. The > > bones in my feet are " lumpy " -- and my ankles have both severe arthritis as > > well as sarcoid granulomas. my Rheumi injected one of the ankle joints to see > > if it would help-- but I got so little relief, he stated that it's sarc > > damage to the bones rather than arthritis. (We get the 'spurs' that many people > > get- but the inflammatory reaction shows that it's not bursitis. LOW ESR > > rates generally--and if it was 'true arthritis'--that sed rate would be way up.) > > > I am thankful that I am on the remicade...this last treatment left > > me very tired for about a week, but my left eye is showing no > > inflamation and the right is very little. So the iritis is settling > > down a lot. I am still having the swelling in my upper inner eye > > lid. Have wondered about seeing an ENT about it..what do you think? > > > Yeah on the iritis! This is excellant. Very excellant! As far as the > eyelids-- an ENT--EAR, NOSE AND THROAT-- isn't gonna help. An Ophthalmologist (EYE > MD) is what you need. > Restasis is showing alot of improvement with helping with those lacrimal tear > glands that are under the eyelids. (The conjuctiva--the white of the eye) > actually goes from the inside of each eyelid starting at the eyelashes, and up > and around the fold of the inside of the eye- then over the eye to where it > connects to the cornea. > There are a large number of lacrimal (tear) glands along the conjuctiva, and > if they are inflammed by dryness or inflammation (even crying dries out your > eyes) so using artificial tears is very, very important. > Restasis is a 'cyclosporine' eye drop, and it reduces the inflammation of > those glands. When the glands become less inflammed, they produce more of the > right balance of tears-- so you're eyes aren't as sore feeling. It is by > prescription-- and the MD can probably give you some samples to try-- along with > Sustane or Hypotears or something on that line. Use the tears as often as you > feel the need (actually more often--since we wait till we're in pain to do > something)-- and use the Eyegel tears at night-- and you'll see a huge difference. > (Use the Restasis as directed--it is an antibiotic type eye drop). > > > My neuro systems are greatly inproved. : )! I see the Neurologist on > > Thursday for a check up and an wondering what he will say. He has > > talked about NS and Multi system Sarcoidis but has never wanted to > > give me that dx. > > Our MD's hate the dx of multi-system or NS. Once they give it to you, they > then throw up their hands -- and arent about to admit they know crap about it. > So that's where we come in. We've gotta learn about it ourself, and take the > info to them. ARRGGH. > > Since the Remicade has shown such great > improvement I hope he will see > > the light now. > > Take in some of the articles written by Dr. Sharma and Dr. Baughman. These > guys are doing everything they can to figure out this disease, and what's > happening is amazing. The American Chest Physicians has some articles by them, as > does the American Rheumatology and Immunology Journals. Neurologists don't > seem to be onboard-- unless we come in with the boat. > > I'll look forward to hearing what your MD's have to say when they see how > well you're doing now that you're on the Remicade. > > Take care, > Tracie > NS co-owner/moderator > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.